Next Article in Journal
LC-MS Profile, Gastrointestinal and Gut Microbiota Stability and Antioxidant Activity of Rhodiola rosea Herb Metabolites: A Comparative Study with Subterranean Organs
Next Article in Special Issue
A Review of the Potential Benefits of Plants Producing Berries in Skin Disorders
Previous Article in Journal
Toxicity of Necrostatin-1 in Parkinson’s Disease Models
Previous Article in Special Issue
Assessment of the In Vivo Antioxidant Activity of an Anthocyanin-Rich Bilberry Extract Using the Caenorhabditis elegans Model
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Antioxidants
Volume 9
Issue 6
10.3390/antiox9060525
antioxidants-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

The AMP-Activated Protein Kinase Plays a Role in Antioxidant Defense and Regulation of Vascular Inflammation

by
Thomas Jansen
1,†,
Miroslava Kvandová
1,†,
Andreas Daiber
1,2,*,
Paul Stamm
1,
Katie Frenis
1,
Eberhard Schulz
3,
Thomas Münzel
1,2 and
Swenja Kröller-Schön
1,*
1
Center for Cardiology, Department of Cardiology 1—Molecular Cardiology, University Medical Center, Johannes Gutenberg University, 55131 Mainz, Germany
2
Partner Site Rhine-Main, German Center for Cardiovascular Research (DZHK), Langenbeckstr. 1, 55131 Mainz, Germany
3
Department of Cardiology, Allgemeines Krankenhaus Celle, 29223 Celle, Germany
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Antioxidants 2020, 9(6), 525; https://doi.org/10.3390/antiox9060525
Submission received: 27 May 2020 / Revised: 10 June 2020 / Accepted: 11 June 2020 / Published: 16 June 2020
(This article belongs to the Special Issue Feature Papers in Antioxidants in 2020)
Browse Figures
Versions Notes

Abstract

:
Cardiovascular diseases represent the leading cause of global deaths and life years spent with a severe disability. Endothelial dysfunction and vascular oxidative stress are early precursors of atherosclerotic processes in the vascular wall, all of which are hallmarks in the development of cardiovascular diseases and predictors of future cardiovascular events. There is growing evidence that inflammatory processes represent a major trigger for endothelial dysfunction, vascular oxidative stress and atherosclerosis and clinical data identified inflammation as a cardiovascular risk factor on its own. AMP-activated protein kinase (AMPK) is a central enzyme of cellular energy balance and metabolism that has been shown to confer cardio-protection and antioxidant defense which thereby contributes to vascular health. Interestingly, AMPK is also redox-regulated itself. We have previously shown that AMPK largely contributes to a healthy endothelium, confers potent antioxidant effects and prevents arterial hypertension. Recently, we provided deep mechanistic insights into the role of AMPK in cardiovascular protection and redox homeostasis by studies on arterial hypertension in endothelial and myelomonocytic cell-specific AMPK knockout (Cadh5CrexAMPKfl/fl and LysMCrexAMPKfl/fl) mice. Using these cell-specific knockout mice, we revealed the potent anti-inflammatory properties of AMPK representing the molecular basis of the antihypertensive effects of AMPK. Here, we discuss our own findings in the context of literature data with respect to the anti-inflammatory and antioxidant effects of AMPK in the specific setting of arterial hypertension as well as cardiovascular diseases in general.

Graphical Abstract

1. Introduction

Cardiovascular diseases are the leading cause of global deaths and life years spent with a severe disability. The most recent report from the World Health Organization revealed an annual loss of life of 17 million due to cardiovascular diseases, and further, that these deaths could be significantly decreased by reduction in tobacco use and mitigation of other lifestyle parameters. (e.g., diet and physical activity) [1]. All these main risk factors cause vascular oxidative stress resulting in endothelial dysfunction and the activation of inflammatory processes, both of which are early precursors of atherosclerotic changes in the vascular wall. As such, oxidative stress, endothelial dysfunction and active inflammation are real hallmarks of the development of cardiovascular diseases and predictors of future cardiovascular events [2,3].
Adenosine monophosphate-activated protein kinase (AMPK) was first described in 1988 by Hardie et al. [4,5], who defined this protein as a regulating enzyme of acetyl-CoA-carboxylase and HMG-CoA-reductase. They named this enzyme for its most prominent physiological activator adenosine monophosphate, AMP [5]. Following the elucidation of AMPK’s energy sensing ability in regulating glucose uptake [6] and securing cellular survival under stress conditions [7], the enzyme became the focus of increased research interest. The function of AMPK as an energy sensor is not just restricted to only intracellular processes, even extracellular energy expenditure is balanced by this heterotrimeric kinase. Once activated, AMPK phosphorylates several downstream targets [6,8,9,10], thereby inhibiting energy consumption and promoting energy production to ensure cellular survival [7]. Besides its role as a central hub in cellular energy utilization, AMPK is also involved in a number of other important biological functions (for review see Kahn et al., [11]), including the recently described regulation of the epigenetic pathways (Figure 1) [11,12]. The first hints of AMPK’s cardiovascular influence were shown in 1999 by Chen et al. who reported direct phosphorylation sites on endothelial NO-Synthase enzyme in endothelial cells and myocytes [13]. The present review focuses on the evidence that AMPK represents a central regulator of vascular inflammation by maintaining the oxidative homeostasis in the cell.

2. AMPK Structure, Activation Process, Targets and Pathways

AMPK is a conserved serine/threonine heterotrimeric kinase, which is known to be a cellular energy sensor. AMPK isoforms are assembled as heterotrimeric complexes that include one catalytic α subunit and two regulatory β and γ subunits (Figure 2) [8]. These different isoforms of subunits (α1/α2, β1/β2, γ1/γ2/γ3) are encoded by separate genes. In total, there are 12 isoforms specifically distributed by cell type according to their unique function [14]. The α subunit contains the kinase domain at its N-terminus, whereas the C-terminal region binds to the ß subunit [15]. The important fuel sensing, carbohydrate-binding domain is located in the β subunit which is also responsible for the interaction with the γ subunit [16]. The individual activation processes take place in a number of domains located in the γ subunit [15]. AMPK activation is delineated in three steps based on the AMP/ATP ratio: phosphorylation by upstream protein kinases, dephosphorylation processes by upstream protein phosphatases and then allosteric activation by AMP or/and ATP. All of these mechanisms ensure that the system is sensitive and responds to small AMP/ATP ratio changes [17,18]. AMP binding and phosphorylation processes cause conformational changes after phosphorylation/dephosphorylation at Thr172 [18,19]. The mechanism of Thr172 phosphorylation and consequent nucleotide binding is regulated by two individual upstream kinases, liver kinase B1 (LKB1) [20,21] and calcium/calmodulin-dependent protein kinase 2 (CaMMK2) [17]. CaMMK2 activation is dependent on intracellular calcium levels and is the leading activator of AMPK in specific cell types [22], including endothelial cells [23], hypothalamic neurons [24] and T-cells [25]. LKB1, in contrast to CaMMK2, is permanently active [17] and known as a master upstream kinase of AMPK and other kinases [22]. The potential for activation by these two master kinases puts AMPK in the position to receive information from several cellular signaling pathways [17].
Pharmacological activation of AMPK can be achieved through the use of five classes of compounds (Figure 2), divided by the activation mechanism [14]. The compounds in class 1 (e.g., berberine or metformin) inhibit the complex I of the mitochondrial respiratory chain, whereas class 2 compounds (e.g., 2-deoxyglucose) inhibit glycolysis [15]. In class 3, AICAR (5-aminoimidazole-4-carboxymide ribonucleoside), widely used as an AMPK activator, is converted to the AMP analog ZMP and mimics the activation process by AMP [26,27]. In class 4, C13 is listed as a specific activator of the α1 subunit. This compound is internalized in the cell, converted to the AMP analog C2 and binds to the γ subunit [28,29,30]. Among the specific AMPK activators, A769662 represents a small molecule that activates AMPK via an allosteric action. Mechanistically, dephosphorylation of active αAMPK at Thr172 is prevented by a reciprocal action with the β1-subunit. Class 5, the last group of activators, are synthetic compounds (e.g., MT63-78, PF-249) which bind at the ADaM site in the β subunit of the AMPK complex [26,31,32,33,34].
A wide range of endogenous physiological stimuli has been found to activate AMPK in the vasculature, including angiotensin II [35], hypoxia [36], shear stress [37], low glucose [38] and oxidative stress [39,40]. Vasoactive substances like thrombin [23], VEGF [41], bradykinin [42] and estrogen [43] also activate AMPK through a CAMKK2-mediated pathway. Additionally, a number of cholesterol-lowering [44,45] and anti-diabetic [46,47,48,49] drugs activate AMPK, which is thought to contribute to their beneficial effects on the cardiovascular system.
Reactive oxygen species may also play a role in the activation of AMPK independently of adenine nucleotides [50,51,52,53]. Several groups have reported AMPK activation in the form of oxidative changes to Cys299 and Cys304 in the catalytic subunit [54] in response to increased concentrations of exogenous H2O2 [35]. These alterations in AMPK’s activity were independent of adenine nucleotides, leading to the hypothesis that AMPK is redox-sensitive [54]. Other regulatory pathways that are related to redox signaling and oxidative stress are based on alterations by SIRT6 [55], as well as the antioxidant and epigenetic drug resveratrol [56].
Though there are numerous activator compounds, there is no specific pharmacological inhibitor of the AMPK complex. The compound C is the only known pharmacological inhibitor, but it is not a specific inhibitor [57]. Thus, to investigate the effects mediated by AMPK inhibition, it is necessary to employ genetic approaches, such as knockout models (global or tissue-/cell-specific) or siRNA/microRNA, among others [58].

3. AMPK in Vascular Oxidative Stress

Endothelial function is predicted by the rate of vascular NO production and simultaneous consumption by reactive oxygen species (ROS). ROS, like the superoxide anion (O2•−), hydrogen peroxide (H2O2) and hydroxyl radical (•OH), are produced physiologically by normal cellular metabolic processes. The predominant source of ROS production during metabolic processes is the mitochondrial electron transport chain, especially Complexes I and III. Within these complexes, a reduction of molecular oxygen by the nicotinamide adenine dinucleotide phosphate (NADPH) oxidases (NOX) produces O2•− [60,61]. Furthermore, NADH-Dehydrogenase in Complex I is also a critical ROS-generating part of the respiratory chain, which could be a useful indicator of the redox state under physiological conditions [54]. Mitochondria are indeed one of the primary sources of intracellular ROS production and are responsible for up to 95% of total ROS levels [62]. Therefore, a system is needed which is able to maintain the redox homeostasis in both normal and stress conditions. Nuclear factor erythroid 2-related factor 2 (Nrf-2) is a master regulator of the antioxidant and anti-inflammatory defense machinery, participating in the maintenance of the cellular redox balance [63]. The ROS-dependent activation of Nrf-2 under normal or stress conditions can be understood as a stress response to secure oxidative homeostasis [64]. The first change in Nrf-2 activity upon conditions of oxidative stress is driven by the phosphorylation of Ser40 by protein kinase Cδ (PKCδ) leading to the release of Nrf-2 from the Nrf-2-Keap-1 complex. The detachment and resulting stabilization of Nrf-2 in the cytosol allows translocation to the nucleus where it binds to antioxidant response element (ARE) regions, stimulating the expression of antioxidant genes [65,66]. This activation process is also mainly regulated by oxidation of the thiol groups in the Keap-1/Nrf2 complex to induce conformational changes allowing subsequent phosphorylation by PKC. Nrf-2 is a highly regulated protein not just in the cytosol, but also in the nucleus. Nuclear Nrf-2 is regulated by the glycogen synthase kinase 3ß and its downstream target Fyn to induce the nuclear export and final degradation of the protein [67]. AMPK is known to be a positive regulator of Nrf-2 by direct phosporylation on Ser550, leading to accumulation in the nucleus to induce the expression of proteins belonging to the antioxidant defence system of the cell [68].
This direct interaction between AMPK and Nrf-2 points to a critical crosstalk between major regulators of metabolism and the redox system of the cell maintaining the necessary homeostasis to secure cellular survival [68]. In addition to this direct redox regulation of AMPK by oxidation of critical cysteine residues [50,51,52], indirect redox signaling/regulation has also been reported. Sobotta et al. illustrated that cytosolic AMPK can be directly activated by reversible thiol oxidation, e.g., peroxiredoxin dimerization [69], or indirectly by redox-sensitive upstream kinases [70,71]. A factor impairing the redox balance is glucose starvation leading to an elevation of intracellular ROS, where activation of AMPK seems to have a critical role in promoting cellular survival [72]. Taken together, AMPK contributes to signal pathways that regulate the redox balance of the cell determining the emergence of cardiovascular diseases [73].

4. AMPK in Endothelial Function

The major factor for the conservation of vascular homeostasis is an intact endothelium, which depends on endothelial nitric oxide synthase (eNOS)-derived NO production. NO is formed by a family of proteins called nitric oxide synthases (NOS) by oxidizing L-arginine under the consumption of molecular oxygen. Endothelium-derived NO is the key player in the regulation of the vascular tone [74,75]. In addition to relaxing vessels, NO exerts anti-inflammatory and antithrombotic effects in the vasculature [76,77,78]. A reduction in the nitric oxide bioavailability leads to endothelial dysfunction which results in hypertension and atherosclerosis [79,80]. There is a myriad of known regulatory mechanisms that affect eNOS activity: including post-translational modifications, availability of cofactors like BH4, protein–protein interactions, prosthetic groups, calcium/calmodulin and several phosphorylation sites [81]. Shear stress, statins and adiponectin are physiological, pharmacological and hormonal stimuli that are known to increase AMPK activity directly and lead to the phosphorylation of eNOS at Ser633/635, increasing the NO bioavailability and/or the antioxidant potential of endothelial cells [74,82,83,84,85,86]. In contrast, inhibition of AMPK—genetically or pharmacologically—decreases the phosphorylation of eNOS at Ser633/635, resulting in impaired NO production [74]. In addition, the group of Fleming and Fisslthaler showed that AMPK is also responsible for the phosphorylation of eNOS at Thr495, which is known to be an inhibitory phosphorylation site [87]. These AMPK-dependent phosphorylation sites of eNOS seem to play a minor role in vivo, suggesting that cardiovascular protection occurs through other pathways, such as the increased bioavailability of NO resulting from improved mitochondrial function (via PGC-1α) or regulation of transcriptional changes of antioxidant and anti-inflammatory enzymes like superoxide dismutase 2 (SOD2) [88]. In accordance with this, global deletion of the vascular isoform of AMPK, α1, elicited neither endothelial dysfunction, a decrease in eNOS phosphorylation on Ser1177 nor a consequent decrease in NO bioavailability [39].
As eNOS is a strongly regulated enzyme, its phosphorylation status is not the only determinant in its activity. Intracellular tetrahydrobiopterin (BH4) levels are essential for dimerization and consequently for the functionality of eNOS [89,90]. Furthermore, BH4 levels are determined by a balance in the rate of synthesis, oxidation and recycling of BH2 to BH4. Production of BH4 is regulated by guanosine-5’-triphosphatecyclohydrolase I (GCH I) [91]. AMPK also affects this aspect of eNOS regulation by suppressing the 26S proteasome-dependent GTPCH I degradation in vitro, reversing diabetes-induced endothelial dysfunction [90]. Due to these links to eNOS regulation, the idea of “AMPK activation as a strategy for protecting vascular endothelial function” was already published in 2008 [92].
Our group showed that angiotensin II infusion (1 mg/kg/d) resulted in significant endothelial dysfunction which was characterized by a dramatic increase in the superoxide signal in the vascular wall as well as an increased myocardial NADPH oxidase activity [35]. The activation of AMPK in this model using daily AICAR injections (200 mg/kg/d) led to a significant improvement of the endothelial dysfunction, diminished superoxide production in the vascular wall and a reduction in myocardial NADPH oxidase activation [35]. Based on these data, we demonstrated that AMPK, especially the isoform α1AMPK, is a protective enzyme in the vascular system. Further evidence showed that AICAR injections were ineffective in AT II-infused α1AMPK or PGC-1α global knockout animals [35]. Furthermore, we were able to show that AT II (low dose 0.1 mg/kg/d) infusion in α1AMPK knockout animals resulted in a more pronounced endothelial dysfunction, oxidative stress and inflammatory response compared with the corresponding wild-type animals. These changes correlated with increased expression of the NADPH oxidase subunit NOX-2 (mRNA and protein), which represents the essential catalytic subunit of the phagocytic NADPH oxidase. Suppression of the NADPH oxidase by in vivo administration of apocynin decreased vascular ROS production and also preserved the vascular inflammatory response as assessed by inducible NO synthase (iNOS), cyclooxygenase-2 (COX-2) and vascular cell adhesion molecule 1 (VCAM-1). However, an important limitation of this study was in the use of global knockout animals, as α1AMPK deletion has effects in a variety of tissues that are not isolated only to vascular tissue. Further, Föller et al. were able to show that α1AMPK plays a decisive role in erythrocyte survival through their demonstration that erythrocytes of α1AMPK global knockout animals have a much shorter lifespan, which leads to a severe splenomegaly [93]. Therefore, a new study was designed using endothelial-specific knockout animals, which lack α1AMPK exclusively in endothelial cells, presenting novel mechanistic insights on the protection of the vasculature against oxidative damage in vivo [94]. Loss of endothelial α1AMPK impairs the endothelial cell barrier function, resulting in an enhanced recruitment of inflammatory cells to the vascular wall (Figure 3A,B). Based on these changes, cytokines and vascular adhesion molecules, as well as inflammatory proteins were upregulated. In this endothelial-specific α1AMPK mouse model, we found that the counterpart of the chemokine C-C chemokine receptor type 2 (CCR2), the ligand monocyte chemoattractant protein-1 (MCP-1) (Figure 3C), significantly increased in the aorta of these mice, which resulted in higher α1AMPK-mediated immune cell infiltration and increased NOX-2 protein expression (Figure 3D). This was accompanied by augmented production of vascular reactive oxygen species (Figure 3E). In addition to the inflammatory response, AT II-induced cytoprotective HO-1 upregulation was suppressed in α1AMPK-deficient cells [94]. In summary, endothelial-specific α1AMPK seems to be a crucial element in the recruitment of inflammatory cells to the vasculature, modulating inflammatory responses and vascular function in a pro-oxidative milieu [94].

5. AMPK in Vascular Inflammation

Inflammation is triggered in response to tissue injury and represents an energy-consuming process. Here, AMPK has been shown to close the gap between metabolism and inflammation since metabolic control of immune cells determines their fate and function. During recent years, it has become apparent that profound knowledge of metabolic pathways within immune cells is important to complete the picture of the pro- and anti-inflammatory response. In this regard, AMPK is known to have anti-inflammatory properties, reported in diverse animal models of inflammation [95,96]. Among immune cells, experimental work is mainly focused on the role of AMPK in T-cells and macrophages [97,98,99]. The functional role of AMPK in T-cells has been studied intensively, shedding light on α1AMPK’s important role in the proliferation and differentiation of CD8+ cytotoxic T lymphocytes. α1AMPK-depleted T-cells showed a striking defect in their ability to generate memory CD8+ T-cell responses during Listeria monocytogenes infection [100]. Alongside this important finding, work by Blagih et al. showed that AMPK couples nutrient availability to T-cell effector function, confirming that α1AMPK was required for the metabolic adaption and following adequate T-cell response in the process of inflammation [101]. Several disease models have been used to uncover important mechanisms beyond AMPK’s physiological functions, especially of the α1 subunit, in the regulation of inflammatory control.
A milestone in the field of immune cell-specific AMPK research was the manuscript by Mounier et al. published in 2013 [102]. They described for the first time the consequences of α1AMPK depletion in myeloid cells in the setting of muscle injury in mice. Macrophages lacking the α1AMPK subunit were dysfunctional, in that they maintained M1 polarization [102]. The number of anti-inflammatory M2 macrophages were decreased, resulting in an impairment of both the release of anti-inflammatory cytokines and phagocytosis of necrotic and apoptotic cells. In this context, we investigated the role of α1AMPK in a model of AT II-induced endothelial dysfunction using a myeloid cell-specific α1AMPK knockout mouse. These animals are characterized by a permanent, non-inducible α1AMPK deletion in myeloid cells and display a pro-inflammatory vascular phenotype in response to specific stimuli (e.g., angiotensin II) [103]. Severe endothelial dysfunction (Figure 4A) and oxidative stress (Figure 4B) with a pronounced F4/80+ macrophage and GR1+ granulocyte infiltration in the vasculature were present in these mice, compared with wild-type control animals. Since CCR2 plays a pivotal role in AT II-induced vascular inflammation (Figure 4C), the increased CCR2 expression on α1AMPK-depleted macrophages caused vascular inflammation with a high secretion of IFN-γ, IL-6 and TNF-α (Figure 4D) [103]. In addition to these reports on disease models, other studies highlighted the physiological role of AMPK in the regulation of immune cells, since the modulation of AMPK activity results in an abolished inflammatory response [104,105,106] and demonstrated a significant reduction in IFN-γ and TNF-α release after AMPK activation with metformin, berberine and AICAR.
Accordingly, AMPK is able to regulate the differentiation of monocytes and the release of inflammatory cytokines in macrophages, leading to the conclusion that AMPK could play an important role in the atherosclerosis-mediated inflammation process through the macrophage-derived foam cell function. Recent work by Chen et al. has shown that the activation of AMPK significantly reduced LOX-1 expression and oxLDL uptake in macrophages, mechanistically by the AMPK-mediated suppression of the NF-kB signaling pathway [107]. Additional work by Zhang et al. supported evidence for a significant role of AMPK in atherosclerosis by showing that activation of AMPK in cultured human endothelial cells resulted in an attenuation of the endothelial pro-inflammatory response, by inhibition of monocyte adhesion and VCAM-1 expression. The NF-kB transcriptional activity was enhanced due to the AMPK-mediated acetylation of p300 HAT activity [108]. Other studies have highlighted the anti-inflammatory properties of AMPK in a model of LPS-induced endothelial inflammation. LPS injection represents a severe sepsis model which is characterized by a strong inflammatory response, triggered by Toll-like receptors 2 and 4. Here, the activation of AMPK with metformin suppressed TLR4 activity [109]. Work by Sun et al. showed that TLR4 protein expression induced by LPS can be prevented by AMPK activation with AICAR in EA.hy926 cells. The activation of AMPK with the alternative activator A769662 resulted in a similar TLR4 modulation. Inhibition of AMPK with the compound C abolished the anti-inflammatory effects, giving evidence for these AMPK-mediated effects [44]. Despite these promising and positive results, the consequences of AMPK activity on the modulation of immune cell function remain uncertain and no data are available in respect to immune cell deficiency, which needs to be addressed in upcoming studies. Further work might focus on the role of AMPK in granulocytes, since these cells display the first response in the cascade of inflammation. However, AMPK is ubiquitously expressed in immune cells and mediates diverse anti-inflammatory responses which might indicate AMPK as a therapeutic target in the future.

6. Conclusions

Over the last decades, increased research interest has been shown in metabolic pathways, especially those involving AMPK, in cardiovascular research. Our understanding of pathologies is continuously improved by more detailed molecular insights into metabolic or inflammatory diseases leading to cardiovascular outcomes, culminating in new therapeutic concepts. Beyond the well-established antioxidant, anti-inflammatory and metabolic protective effects mediated by AMPK, there are also novel pathways in the focus of current and future research detailing the overall cardio-protective effects of AMPK (summarized in Figure 5). The summarized data about the effect of AMPK on cardiovascular diseases are more than promising, but remain limited due to its generation in animal models. Especially the application of cell-specific knockout models provided an important gain of knowledge about the pathophysiologic basis of AMPK-mediated vascular effects. It is necessary to translate these findings in the setting of human disease. An important next step toward accomplishing this translation is to determine the role of α1AMPK in patients with severe hypertension or endothelial dysfunction. In this regard, the AMPK-dependent myeloid cell function should be addressed as well as the T-cell function, since we know that these cells play an important role in the genesis of hypertension. Based on our data provided, α1AMPK might have important functions in this setting. Future research then must determine whether AMPK is involved in the genetic alterations that may influence aging-related cardiovascular diseases, like hypertension and coronary artery disease. Overall, AMPK represents a prime target for future investigation that will result in applicable therapies against inflammation-associated cardiovascular diseases.

Author Contributions

T.J., M.K., A.D., E.S., T.M. and S.K.-S. wrote the manuscript; P.S. and K.F. made critical revisions and contribution to the discussion. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the German Research Foundation (DFG SCHU 1486/4-1 to E.S.). Thomas Münzel is PI of the DZHK (German Center for Cardiovascular Research), Partner Site Rhine-Main, Mainz, Germany.

Acknowledgments

The assistance by our graphical designer Margot Neuser in preparing the schemes is gratefully acknowledged.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Roth, G.A.; Johnson, C.; Abajobir, A.; Abd-Allah, F.; Abera, S.F.; Abyu, G.; Ahmed, M.; Aksut, B.; Alam, T.; Alam, K.; et al. Global, Regional, and National Burden of Cardiovascular Diseases for 10 Causes, 1990 to 2015. J. Am. Coll. Cardiol. 2017, 70, 1–25. [Google Scholar] [CrossRef]
  2. Daiber, A.; Steven, S.; Weber, A.; Shuvaev, V.V.; Muzykantov, V.R.; Laher, I.; Li, H.; Lamas, S.; Munzel, T. Targeting vascular (endothelial) dysfunction. Br. J. Pharmacol. 2017, 174, 1591–1619. [Google Scholar] [CrossRef]
  3. Munzel, T.; Hink, U.; Heitzer, T.; Meinertz, T. Role for NADPH/NADH oxidase in the modulation of vascular tone. Ann. N. Y. Acad. Sci. 1999, 874, 386–400. [Google Scholar] [CrossRef]
  4. Carling, D.; Clarke, P.R.; Zammit, V.A.; Hardie, D.G. Purification and characterization of the AMP-activated protein kinase. Copurification of acetyl-CoA carboxylase kinase and 3-hydroxy-3-methylglutaryl-CoA reductase kinase activities. Eur. J. Biochem. 1989, 186, 129–136. [Google Scholar] [CrossRef] [PubMed]
  5. Sim, A.T.; Hardie, D.G. The low activity of acetyl-CoA carboxylase in basal and glucagon-stimulated hepatocytes is due to phosphorylation by the AMP-activated protein kinase and not cyclic AMP-dependent protein kinase. FEBS Lett. 1988, 233, 294–298. [Google Scholar] [CrossRef] [Green Version]
  6. Hardie, D.G.; Carling, D. The AMP-activated protein kinase--fuel gauge of the mammalian cell? Eur. J. Biochem. 1997, 246, 259–273. [Google Scholar] [CrossRef] [PubMed]
  7. Corton, J.M.; Gillespie, J.G.; Hardie, D.G. Role of the AMP-activated protein kinase in the cellular stress response. Curr. Biol. 1994, 4, 315–324. [Google Scholar] [CrossRef]
  8. Hardie, D.G.; Scott, J.W.; Pan, D.A.; Hudson, E.R. Management of cellular energy by the AMP-activated protein kinase system. FEBS Lett. 2003, 546, 113–120. [Google Scholar] [CrossRef]
  9. Hardie, D.G.; Carling, D.; Carlson, M. The AMP-activated/SNF1 protein kinase subfamily: Metabolic sensors of the eukaryotic cell? Annu. Rev. Biochem. 1998, 67, 821–855. [Google Scholar] [CrossRef]
  10. Carling, D. The AMP-activated protein kinase cascade--a unifying system for energy control. Trends Biochem. Sci. 2004, 29, 18–24. [Google Scholar] [CrossRef]
  11. Kahn, B.B.; Alquier, T.; Carling, D.; Hardie, D.G. AMP-activated protein kinase: Ancient energy gauge provides clues to modern understanding of metabolism. Cell Metab. 2005, 1, 15–25. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Gongol, B.; Sari, I.; Bryant, T.; Rosete, G.; Marin, T. AMPK: An Epigenetic Landscape Modulator. Int. J. Mol. Sci. 2018, 19, 3238. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Chen, Z.P.; Mitchelhill, K.I.; Michell, B.J.; Stapleton, D.; Rodriguez-Crespo, I.; Witters, L.A.; Power, D.A.; Ortiz de Montellano, P.R.; Kemp, B.E. AMP-activated protein kinase phosphorylation of endothelial NO synthase. FEBS Lett. 1999, 443, 285–289. [Google Scholar] [CrossRef] [Green Version]
  14. Salt, I.P.; Hardie, D.G. AMP-Activated Protein Kinase: An Ubiquitous Signaling Pathway with Key Roles in the Cardiovascular System. Circ. Res. 2017, 120, 1825–1841. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Hardie, D.G.; Hawley, S.A.; Scott, J.W. AMP-activated protein kinase--development of the energy sensor concept. J. Physiol. 2006, 574, 7–15. [Google Scholar] [CrossRef]
  16. Polekhina, G.; Gupta, A.; Michell, B.J.; van Denderen, B.; Murthy, S.; Feil, S.C.; Jennings, I.G.; Campbell, D.J.; Witters, L.A.; Parker, M.W.; et al. AMPK beta subunit targets metabolic stress sensing to glycogen. Curr. Biol. 2003, 13, 867–871. [Google Scholar] [CrossRef] [Green Version]
  17. Hardie, D.G. Keeping the home fires burning: AMP-activated protein kinase. J. R. Soc. Interface 2018, 15. [Google Scholar] [CrossRef]
  18. Li, X.; Wang, L.; Zhou, X.E.; Ke, J.; de Waal, P.W.; Gu, X.; Tan, M.H.; Wang, D.; Wu, D.; Xu, H.E.; et al. Structural basis of AMPK regulation by adenine nucleotides and glycogen. Cell Res. 2015, 25, 50–66. [Google Scholar] [CrossRef] [Green Version]
  19. Xiao, B.; Sanders, M.J.; Underwood, E.; Heath, R.; Mayer, F.V.; Carmena, D.; Jing, C.; Walker, P.A.; Eccleston, J.F.; Haire, L.F.; et al. Structure of mammalian AMPK and its regulation by ADP. Nature 2011, 472, 230–233. [Google Scholar] [CrossRef] [Green Version]
  20. Hawley, S.A.; Boudeau, J.; Reid, J.L.; Mustard, K.J.; Udd, L.; Makela, T.P.; Alessi, D.R.; Hardie, D.G. Complexes between the LKB1 tumor suppressor, STRAD alpha/beta and MO25 alpha/beta are upstream kinases in the AMP-activated protein kinase cascade. J. Biol. 2003, 2, 28. [Google Scholar] [CrossRef] [Green Version]
  21. Woods, A.; Johnstone, S.R.; Dickerson, K.; Leiper, F.C.; Fryer, L.G.; Neumann, D.; Schlattner, U.; Wallimann, T.; Carlson, M.; Carling, D. LKB1 is the upstream kinase in the AMP-activated protein kinase cascade. Curr. Biol. 2003, 13, 2004–2008. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Shackelford, D.B.; Shaw, R.J. The LKB1-AMPK pathway: Metabolism and growth control in tumour suppression. Nat. Rev. Cancer 2009, 9, 563–575. [Google Scholar] [CrossRef] [PubMed]
  23. Stahmann, N.; Woods, A.; Carling, D.; Heller, R. Thrombin activates AMP-activated protein kinase in endothelial cells via a pathway involving Ca2+/calmodulin-dependent protein kinase kinase beta. Mol. Cell. Biol. 2006, 26, 5933–5945. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Anderson, K.A.; Ribar, T.J.; Lin, F.; Noeldner, P.K.; Green, M.F.; Muehlbauer, M.J.; Witters, L.A.; Kemp, B.E.; Means, A.R. Hypothalamic CaMKK2 contributes to the regulation of energy balance. Cell Metab. 2008, 7, 377–388. [Google Scholar] [CrossRef] [Green Version]
  25. Tamas, P.; Hawley, S.A.; Clarke, R.G.; Mustard, K.J.; Green, K.; Hardie, D.G.; Cantrell, D.A. Regulation of the energy sensor AMP-activated protein kinase by antigen receptor and Ca2+ in T lymphocytes. J. Exp. Med. 2006, 203, 1665–1670. [Google Scholar] [CrossRef] [Green Version]
  26. Hawley, S.A.; Ross, F.A.; Chevtzoff, C.; Green, K.A.; Evans, A.; Fogarty, S.; Towler, M.C.; Brown, L.J.; Ogunbayo, O.A.; Evans, A.M.; et al. Use of cells expressing gamma subunit variants to identify diverse mechanisms of AMPK activation. Cell Metab. 2010, 11, 554–565. [Google Scholar] [CrossRef] [Green Version]
  27. Corton, J.M.; Gillespie, J.G.; Hawley, S.A.; Hardie, D.G. 5-aminoimidazole-4-carboxamide ribonucleoside. A specific method for activating AMP-activated protein kinase in intact cells? Eur. J. Biochem. 1995, 229, 558–565. [Google Scholar] [CrossRef]
  28. Gomez-Galeno, J.E.; Dang, Q.; Nguyen, T.H.; Boyer, S.H.; Grote, M.P.; Sun, Z.; Chen, M.; Craigo, W.A.; van Poelje, P.D.; MacKenna, D.A.; et al. A Potent and Selective AMPK Activator That Inhibits de Novo Lipogenesis. ACS Med. Chem. Lett. 2010, 1, 478–482. [Google Scholar] [CrossRef] [Green Version]
  29. Langendorf, C.G.; Ngoei, K.R.W.; Scott, J.W.; Ling, N.X.Y.; Issa, S.M.A.; Gorman, M.A.; Parker, M.W.; Sakamoto, K.; Oakhill, J.S.; Kemp, B.E. Structural basis of allosteric and synergistic activation of AMPK by furan-2-phosphonic derivative C2 binding. Nat. Commun. 2016, 7, 10912. [Google Scholar] [CrossRef]
  30. Hunter, R.W.; Foretz, M.; Bultot, L.; Fullerton, M.D.; Deak, M.; Ross, F.A.; Hawley, S.A.; Shpiro, N.; Viollet, B.; Barron, D.; et al. Mechanism of action of compound-13: An alpha1-selective small molecule activator of AMPK. Chem. Biol. 2014, 21, 866–879. [Google Scholar] [CrossRef] [Green Version]
  31. Calabrese, M.F.; Rajamohan, F.; Harris, M.S.; Caspers, N.L.; Magyar, R.; Withka, J.M.; Wang, H.; Borzilleri, K.A.; Sahasrabudhe, P.V.; Hoth, L.R.; et al. Structural basis for AMPK activation: Natural and synthetic ligands regulate kinase activity from opposite poles by different molecular mechanisms. Structure 2014, 22, 1161–1172. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  32. Salatto, C.T.; Miller, R.A.; Cameron, K.O.; Cokorinos, E.; Reyes, A.; Ward, J.; Calabrese, M.F.; Kurumbail, R.G.; Rajamohan, F.; Kalgutkar, A.S.; et al. Selective Activation of AMPK beta1-Containing Isoforms Improves Kidney Function in a Rat Model of Diabetic Nephropathy. J. Pharmacol. Exp. Ther. 2017, 361, 303–311. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Cool, B.; Zinker, B.; Chiou, W.; Kifle, L.; Cao, N.; Perham, M.; Dickinson, R.; Adler, A.; Gagne, G.; Iyengar, R.; et al. Identification and characterization of a small molecule AMPK activator that treats key components of type 2 diabetes and the metabolic syndrome. Cell Metab. 2006, 3, 403–416. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Zadra, G.; Photopoulos, C.; Tyekucheva, S.; Heidari, P.; Weng, Q.P.; Fedele, G.; Liu, H.; Scaglia, N.; Priolo, C.; Sicinska, E.; et al. A novel direct activator of AMPK inhibits prostate cancer growth by blocking lipogenesis. EMBO Mol. Med. 2014, 6, 519–538. [Google Scholar] [CrossRef]
  35. Schulz, E.; Dopheide, J.; Schuhmacher, S.; Thomas, S.R.; Chen, K.; Daiber, A.; Wenzel, P.; Munzel, T.; Keaney, J.F., Jr. Suppression of the JNK pathway by induction of a metabolic stress response prevents vascular injury and dysfunction. Circulation 2008, 118, 1347–1357. [Google Scholar] [CrossRef] [Green Version]
  36. Nagata, D.; Mogi, M.; Walsh, K. AMP-activated protein kinase (AMPK) signaling in endothelial cells is essential for angiogenesis in response to hypoxic stress. J. Biol. Chem. 2003, 278, 31000–31006. [Google Scholar] [CrossRef] [Green Version]
  37. Fisslthaler, B.; Fleming, I.; Keseru, B.; Walsh, K.; Busse, R. Fluid shear stress and NO decrease the activity of the hydroxy-methylglutaryl coenzyme A reductase in endothelial cells via the AMP-activated protein kinase and FoxO1. Circ. Res. 2007, 100, e12–e21. [Google Scholar] [CrossRef] [Green Version]
  38. Wang, J.; Alexanian, A.; Ying, R.; Kizhakekuttu, T.J.; Dharmashankar, K.; Vasquez-Vivar, J.; Gutterman, D.D.; Widlansky, M.E. Acute exposure to low glucose rapidly induces endothelial dysfunction and mitochondrial oxidative stress: Role for AMP kinase. Arterioscler. Thromb. Vasc. Biol. 2012, 32, 712–720. [Google Scholar] [CrossRef] [Green Version]
  39. Schuhmacher, S.; Foretz, M.; Knorr, M.; Jansen, T.; Hortmann, M.; Wenzel, P.; Oelze, M.; Kleschyov, A.L.; Daiber, A.; Keaney, J.F., Jr.; et al. alpha1AMP-activated protein kinase preserves endothelial function during chronic angiotensin II treatment by limiting Nox2 upregulation. Arterioscler. Thromb. Vasc. Biol. 2011, 31, 560–566. [Google Scholar] [CrossRef] [Green Version]
  40. Wang, S.; Zhang, M.; Liang, B.; Xu, J.; Xie, Z.; Liu, C.; Viollet, B.; Yan, D.; Zou, M.H. AMPKalpha2 deletion causes aberrant expression and activation of NAD(P)H oxidase and consequent endothelial dysfunction in vivo: Role of 26S proteasomes. Circ. Res. 2010, 106, 1117–1128. [Google Scholar] [CrossRef] [Green Version]
  41. Reihill, J.A.; Ewart, M.A.; Salt, I.P. The role of AMP-activated protein kinase in the functional effects of vascular endothelial growth factor-A and -B in human aortic endothelial cells. Vasc. Cell 2011, 3, 9. [Google Scholar] [CrossRef] [Green Version]
  42. Mount, P.F.; Lane, N.; Venkatesan, S.; Steinberg, G.R.; Fraser, S.A.; Kemp, B.E.; Power, D.A. Bradykinin stimulates endothelial cell fatty acid oxidation by CaMKK-dependent activation of AMPK. Atherosclerosis 2008, 200, 28–36. [Google Scholar] [CrossRef] [PubMed]
  43. Yang, S.; Wang, J. Estrogen Activates AMP-Activated Protein Kinase in Human Endothelial Cells via ERbeta/Ca(2+)/Calmodulin-Dependent Protein Kinase Kinase beta Pathway. Cell Biochem. Biophys. 2015, 72, 701–707. [Google Scholar] [CrossRef] [PubMed]
  44. Sun, W.; Lee, T.S.; Zhu, M.; Gu, C.; Wang, Y.; Zhu, Y.; Shyy, J.Y. Statins activate AMP-activated protein kinase in vitro and in vivo. Circulation 2006, 114, 2655–2662. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Murakami, H.; Murakami, R.; Kambe, F.; Cao, X.; Takahashi, R.; Asai, T.; Hirai, T.; Numaguchi, Y.; Okumura, K.; Seo, H.; et al. Fenofibrate activates AMPK and increases eNOS phosphorylation in HUVEC. Biochem. Biophys. Res. Commun. 2006, 341, 973–978. [Google Scholar] [CrossRef]
  46. Ceolotto, G.; Gallo, A.; Papparella, I.; Franco, L.; Murphy, E.; Iori, E.; Pagnin, E.; Fadini, G.P.; Albiero, M.; Semplicini, A.; et al. Rosiglitazone reduces glucose-induced oxidative stress mediated by NAD(P)H oxidase via AMPK-dependent mechanism. Arterioscler. Thromb. Vasc. Biol. 2007, 27, 2627–2633. [Google Scholar] [CrossRef] [Green Version]
  47. Rutherford, C.; Speirs, C.; Williams, J.J.; Ewart, M.A.; Mancini, S.J.; Hawley, S.A.; Delles, C.; Viollet, B.; Costa-Pereira, A.P.; Baillie, G.S.; et al. Phosphorylation of Janus kinase 1 (JAK1) by AMP-activated protein kinase (AMPK) links energy sensing to anti-inflammatory signaling. Sci. Signal. 2016, 9, ra109. [Google Scholar] [CrossRef] [Green Version]
  48. Hwang, H.J.; Chung, H.S.; Jung, T.W.; Ryu, J.Y.; Hong, H.C.; Seo, J.A.; Kim, S.G.; Kim, N.H.; Choi, K.M.; Choi, D.S.; et al. The dipeptidyl peptidase-IV inhibitor inhibits the expression of vascular adhesion molecules and inflammatory cytokines in HUVECs via Akt- and AMPK-dependent mechanisms. Mol. Cell Endocrinol. 2015, 405, 25–34. [Google Scholar] [CrossRef]
  49. Krasner, N.M.; Ido, Y.; Ruderman, N.B.; Cacicedo, J.M. Glucagon-like peptide-1 (GLP-1) analog liraglutide inhibits endothelial cell inflammation through a calcium and AMPK dependent mechanism. PLoS ONE 2014, 9, e97554. [Google Scholar] [CrossRef] [Green Version]
  50. Zmijewski, J.W.; Banerjee, S.; Bae, H.; Friggeri, A.; Lazarowski, E.R.; Abraham, E. Exposure to hydrogen peroxide induces oxidation and activation of AMP-activated protein kinase. J. Biol. Chem. 2010, 285, 33154–33164. [Google Scholar] [CrossRef] [Green Version]
  51. Mungai, P.T.; Waypa, G.B.; Jairaman, A.; Prakriya, M.; Dokic, D.; Ball, M.K.; Schumacker, P.T. Hypoxia triggers AMPK activation through reactive oxygen species-mediated activation of calcium release-activated calcium channels. Mol. Cell. Biol. 2011, 31, 3531–3545. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  52. Auciello, F.R.; Ross, F.A.; Ikematsu, N.; Hardie, D.G. Oxidative stress activates AMPK in cultured cells primarily by increasing cellular AMP and/or ADP. FEBS Lett. 2014, 588, 3361–3366. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Han, Y.; Wang, Q.; Song, P.; Zhu, Y.; Zou, M.H. Redox regulation of the AMP-activated protein kinase. PLoS ONE 2010, 5, e15420. [Google Scholar] [CrossRef] [PubMed]
  54. Hinchy, E.C.; Gruszczyk, A.V.; Willows, R.; Navaratnam, N.; Hall, A.R.; Bates, G.; Bright, T.P.; Krieg, T.; Carling, D.; Murphy, M.P. Mitochondria-derived ROS activate AMP-activated protein kinase (AMPK) indirectly. J. Biol. Chem. 2018, 293, 17208–17217. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Cui, X.; Yao, L.; Yang, X.; Gao, Y.; Fang, F.; Zhang, J.; Wang, Q.; Chang, Y. SIRT6 regulates metabolic homeostasis in skeletal muscle through activation of AMPK. Am. J. Physiol. Endocrinol. Metab. 2017, 313, E493–E505. [Google Scholar] [CrossRef] [PubMed]
  56. Zhou, T.; Yan, Y.; Zhao, C.; Xu, Y.; Wang, Q.; Xu, N. Resveratrol improves osteogenic differentiation of senescent bone mesenchymal stem cells through inhibiting endogenous reactive oxygen species production via AMPK activation. Redox Rep. 2019, 24, 62–69. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Bain, J.; Plater, L.; Elliott, M.; Shpiro, N.; Hastie, C.J.; McLauchlan, H.; Klevernic, I.; Arthur, J.S.; Alessi, D.R.; Cohen, P. The selectivity of protein kinase inhibitors: A further update. Biochem. J. 2007, 408, 297–315. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  58. Viollet, B.; Athea, Y.; Mounier, R.; Guigas, B.; Zarrinpashneh, E.; Horman, S.; Lantier, L.; Hebrard, S.; Devin-Leclerc, J.; Beauloye, C.; et al. AMPK: Lessons from transgenic and knockout animals. Front. Biosci. (Landmark Ed) 2009, 14, 19–44. [Google Scholar] [CrossRef] [Green Version]
  59. Hardie, D.G. AMPK–sensing energy while talking to other signaling pathways. Cell Metab. 2014, 20, 939–952. [Google Scholar] [CrossRef] [Green Version]
  60. Brand, M.D. The sites and topology of mitochondrial superoxide production. Exp. Gerontol. 2010, 45, 466–472. [Google Scholar] [CrossRef] [Green Version]
  61. Lambeth, J.D. NOX enzymes and the biology of reactive oxygen. Nat. Rev. Immunol. 2004, 4, 181–189. [Google Scholar] [CrossRef] [PubMed]
  62. Zhang, J.; Wang, Y.; Liu, X.; Dagda, R.K.; Zhang, Y. How AMPK and PKA Interplay to Regulate Mitochondrial Function and Survival in Models of Ischemia and Diabetes. Oxid. Med. Cell. Longev. 2017, 2017, 4353510. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  63. Itoh, K.; Chiba, T.; Takahashi, S.; Ishii, T.; Igarashi, K.; Katoh, Y.; Oyake, T.; Hayashi, N.; Satoh, K.; Hatayama, I.; et al. An Nrf2/small Maf heterodimer mediates the induction of phase II detoxifying enzyme genes through antioxidant response elements. Biochem. Biophys. Res. Commun. 1997, 236, 313–322. [Google Scholar] [CrossRef] [PubMed]
  64. Cullinan, S.B.; Diehl, J.A. PERK-dependent activation of Nrf2 contributes to redox homeostasis and cell survival following endoplasmic reticulum stress. J. Biol. Chem. 2004, 279, 20108–20117. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  65. Huang, H.C.; Nguyen, T.; Pickett, C.B. Phosphorylation of Nrf2 at Ser-40 by protein kinase C regulates antioxidant response element-mediated transcription. J. Biol. Chem. 2002, 277, 42769–42774. [Google Scholar] [CrossRef] [Green Version]
  66. Niture, S.K.; Jain, A.K.; Jaiswal, A.K. Antioxidant-induced modification of INrf2 cysteine 151 and PKC-delta-mediated phosphorylation of Nrf2 serine 40 are both required for stabilization and nuclear translocation of Nrf2 and increased drug resistance. J. Cell Sci. 2009, 122, 4452–4464. [Google Scholar] [CrossRef] [Green Version]
  67. Jain, A.K.; Jaiswal, A.K. GSK-3beta acts upstream of Fyn kinase in regulation of nuclear export and degradation of NF-E2 related factor 2. J. Biol. Chem. 2007, 282, 16502–16510. [Google Scholar] [CrossRef] [Green Version]
  68. Joo, M.S.; Kim, W.D.; Lee, K.Y.; Kim, J.H.; Koo, J.H.; Kim, S.G. AMPK Facilitates Nuclear Accumulation of Nrf2 by Phosphorylating at Serine 550. Mol. Cell. Biol. 2016, 36, 1931–1942. [Google Scholar] [CrossRef] [Green Version]
  69. Sobotta, M.C.; Barata, A.G.; Schmidt, U.; Mueller, S.; Millonig, G.; Dick, T.P. Exposing cells to H2O2: A quantitative comparison between continuous low-dose and one-time high-dose treatments. Free Radic. Biol. Med. 2013, 60, 325–335. [Google Scholar] [CrossRef]
  70. Murphy, M.P. Mitochondrial thiols in antioxidant protection and redox signaling: Distinct roles for glutathionylation and other thiol modifications. Antioxid. Redox Signal. 2012, 16, 476–495. [Google Scholar] [CrossRef]
  71. Sobotta, M.C.; Liou, W.; Stocker, S.; Talwar, D.; Oehler, M.; Ruppert, T.; Scharf, A.N.; Dick, T.P. Peroxiredoxin-2 and STAT3 form a redox relay for H2O2 signaling. Nat. Chem. Biol. 2015, 11, 64–70. [Google Scholar] [CrossRef] [PubMed]
  72. Ren, Y.; Shen, H.M. Critical role of AMPK in redox regulation under glucose starvation. Redox Biol. 2019, 101154. [Google Scholar] [CrossRef] [PubMed]
  73. Wang, S.; Song, P.; Zou, M.H. AMP-activated protein kinase, stress responses and cardiovascular diseases. Clin. Sci. (Lond) 2012, 122, 555–573. [Google Scholar] [CrossRef] [Green Version]
  74. Chen, Z.; Peng, I.C.; Sun, W.; Su, M.I.; Hsu, P.H.; Fu, Y.; Zhu, Y.; DeFea, K.; Pan, S.; Tsai, M.D.; et al. AMP-activated protein kinase functionally phosphorylates endothelial nitric oxide synthase Ser633. Circ. Res. 2009, 104, 496–505. [Google Scholar] [CrossRef] [PubMed]
  75. Furchgott, R.F.; Zawadzki, J.V. The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine. Nature 1980, 288, 373–376. [Google Scholar] [CrossRef] [PubMed]
  76. Lerman, A.; Zeiher, A.M. Endothelial function: Cardiac events. Circulation 2005, 111, 363–368. [Google Scholar] [CrossRef]
  77. Loscalzo, J. Nitric oxide insufficiency, platelet activation, and arterial thrombosis. Circ. Res. 2001, 88, 756–762. [Google Scholar] [CrossRef] [Green Version]
  78. Moncada, S.; Palmer, R.M.; Higgs, E.A. Nitric oxide: Physiology, pathophysiology, and pharmacology. Pharmacol. Rev. 1991, 43, 109–142. [Google Scholar]
  79. Naseem, K.M. The role of nitric oxide in cardiovascular diseases. Mol. Asp. Med. 2005, 26, 33–65. [Google Scholar] [CrossRef]
  80. Rochette, L.; Lorin, J.; Zeller, M.; Guilland, J.C.; Lorgis, L.; Cottin, Y.; Vergely, C. Nitric oxide synthase inhibition and oxidative stress in cardiovascular diseases: Possible therapeutic targets? Pharmacol. Ther. 2013, 140, 239–257. [Google Scholar] [CrossRef]
  81. Bauer, P.M.; Fulton, D.; Boo, Y.C.; Sorescu, G.P.; Kemp, B.E.; Jo, H.; Sessa, W.C. Compensatory phosphorylation and protein-protein interactions revealed by loss of function and gain of function mutants of multiple serine phosphorylation sites in endothelial nitric-oxide synthase. J. Biol. Chem. 2003, 278, 14841–14849. [Google Scholar] [CrossRef] [Green Version]
  82. Davis, B.J.; Xie, Z.; Viollet, B.; Zou, M.H. Activation of the AMP-activated kinase by antidiabetes drug metformin stimulates nitric oxide synthesis in vivo by promoting the association of heat shock protein 90 and endothelial nitric oxide synthase. Diabetes 2006, 55, 496–505. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  83. Zou, M.H.; Hou, X.Y.; Shi, C.M.; Nagata, D.; Walsh, K.; Cohen, R.A. Modulation by peroxynitrite of Akt- and AMP-activated kinase-dependent Ser1179 phosphorylation of endothelial nitric oxide synthase. J. Biol. Chem. 2002, 277, 32552–32557. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  84. Ghimire, K.; Zaric, J.; Alday-Parejo, B.; Seebach, J.; Bousquenaud, M.; Stalin, J.; Bieler, G.; Schnittler, H.J.; Ruegg, C. MAGI1 Mediates eNOS Activation and NO Production in Endothelial Cells in Response to Fluid Shear Stress. Cells 2019, 8, 388. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  85. Kojda, G.; Cheng, Y.C.; Burchfield, J.; Harrison, D.G. Dysfunctional regulation of endothelial nitric oxide synthase (eNOS) expression in response to exercise in mice lacking one eNOS gene. Circulation 2001, 103, 2839–2844. [Google Scholar] [CrossRef] [Green Version]
  86. Kroller-Schon, S.; Jansen, T.; Hauptmann, F.; Schuler, A.; Heeren, T.; Hausding, M.; Oelze, M.; Viollet, B.; Keaney, J.F., Jr.; Wenzel, P.; et al. alpha1AMP-activated protein kinase mediates vascular protective effects of exercise. Arterioscler. Thromb. Vasc. Biol. 2012, 32, 1632–1641. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  87. Zippel, N.; Loot, A.E.; Stingl, H.; Randriamboavonjy, V.; Fleming, I.; Fisslthaler, B. Endothelial AMP-Activated Kinase alpha1 Phosphorylates eNOS on Thr495 and Decreases Endothelial NO Formation. Int. J. Mol. Sci. 2018, 19, 2753. [Google Scholar] [CrossRef] [Green Version]
  88. Zippel, N.; Malik, R.A.; Fromel, T.; Popp, R.; Bess, E.; Strilic, B.; Wettschureck, N.; Fleming, I.; Fisslthaler, B. Transforming growth factor-beta-activated kinase 1 regulates angiogenesis via AMP-activated protein kinase-alpha1 and redox balance in endothelial cells. Arterioscler. Thromb. Vasc. Biol. 2013, 33, 2792–2799. [Google Scholar] [CrossRef] [Green Version]
  89. Stroes, E.; Kastelein, J.; Cosentino, F.; Erkelens, W.; Wever, R.; Koomans, H.; Luscher, T.; Rabelink, T. Tetrahydrobiopterin restores endothelial function in hypercholesterolemia. J. Clin. Investig. 1997, 99, 41–46. [Google Scholar] [CrossRef]
  90. Wang, S.; Xu, J.; Song, P.; Viollet, B.; Zou, M.H. In vivo activation of AMP-activated protein kinase attenuates diabetes-enhanced degradation of GTP cyclohydrolase I. Diabetes 2009, 58, 1893–1901. [Google Scholar] [CrossRef] [Green Version]
  91. Moens, A.L.; Kass, D.A. Tetrahydrobiopterin and cardiovascular disease. Arterioscler. Thromb. Vasc. Biol. 2006, 26, 2439–2444. [Google Scholar] [CrossRef]
  92. Zou, M.H.; Wu, Y. AMP-activated protein kinase activation as a strategy for protecting vascular endothelial function. Clin. Exp. Pharmacol. Physiol. 2008, 35, 535–545. [Google Scholar] [CrossRef] [Green Version]
  93. Foller, M.; Sopjani, M.; Koka, S.; Gu, S.; Mahmud, H.; Wang, K.; Floride, E.; Schleicher, E.; Schulz, E.; Munzel, T.; et al. Regulation of erythrocyte survival by AMP-activated protein kinase. FASEB J. 2009, 23, 1072–1080. [Google Scholar] [CrossRef]
  94. Kroller-Schon, S.; Jansen, T.; Tran, T.L.P.; Kvandova, M.; Kalinovic, S.; Oelze, M.; Keaney, J.F., Jr.; Foretz, M.; Viollet, B.; Daiber, A.; et al. Endothelial alpha1AMPK modulates angiotensin II-mediated vascular inflammation and dysfunction. Basic Res. Cardiol. 2019, 114, 8. [Google Scholar] [CrossRef]
  95. Wang, J.; Hu, S.; Jiang, W.; Song, W.; Cai, L.; Wang, J. Fucoidan from sea cucumber may improve hepatic inflammatory response and insulin resistance in mice. Int. Immunopharmacol. 2016, 31, 15–23. [Google Scholar] [CrossRef]
  96. Hattori, Y.; Suzuki, K.; Hattori, S.; Kasai, K. Metformin inhibits cytokine-induced nuclear factor kappaB activation via AMP-activated protein kinase activation in vascular endothelial cells. Hypertension 2006, 47, 1183–1188. [Google Scholar] [CrossRef] [Green Version]
  97. Titov, A.A.; Baker, H.V.; Brusko, T.M.; Sobel, E.S.; Morel, L. Metformin Inhibits the Type 1 IFN Response in Human CD4(+) T Cells. J. Immunol. 2019, 203, 338–348. [Google Scholar] [CrossRef]
  98. Jing, Y.; Wu, F.; Li, D.; Yang, L.; Li, Q.; Li, R. Metformin improves obesity-associated inflammation by altering macrophages polarization. Mol. Cell. Endocrinol. 2018, 461, 256–264. [Google Scholar] [CrossRef]
  99. Ma, E.H.; Poffenberger, M.C.; Wong, A.H.; Jones, R.G. The role of AMPK in T cell metabolism and function. Curr. Opin. Immunol. 2017, 46, 45–52. [Google Scholar] [CrossRef]
  100. Rolf, J.; Zarrouk, M.; Finlay, D.K.; Foretz, M.; Viollet, B.; Cantrell, D.A. AMPKalpha1: A glucose sensor that controls CD8 T-cell memory. Eur. J. Immunol. 2013, 43, 889–896. [Google Scholar] [CrossRef] [Green Version]
  101. Blagih, J.; Coulombe, F.; Vincent, E.E.; Dupuy, F.; Galicia-Vazquez, G.; Yurchenko, E.; Raissi, T.C.; van der Windt, G.J.; Viollet, B.; Pearce, E.L.; et al. The energy sensor AMPK regulates T cell metabolic adaptation and effector responses in vivo. Immunity 2015, 42, 41–54. [Google Scholar] [CrossRef] [Green Version]
  102. Mounier, R.; Theret, M.; Arnold, L.; Cuvellier, S.; Bultot, L.; Goransson, O.; Sanz, N.; Ferry, A.; Sakamoto, K.; Foretz, M.; et al. AMPKalpha1 regulates macrophage skewing at the time of resolution of inflammation during skeletal muscle regeneration. Cell Metab. 2013, 18, 251–264. [Google Scholar] [CrossRef] [Green Version]
  103. Jansen, T.; Kroller-Schon, S.; Schonfelder, T.; Foretz, M.; Viollet, B.; Daiber, A.; Oelze, M.; Brandt, M.; Steven, S.; Kvandova, M.; et al. alpha1AMPK deletion in myelomonocytic cells induces a pro-inflammatory phenotype and enhances angiotensin II-induced vascular dysfunction. Cardiovasc. Res. 2018, 114, 1883–1893. [Google Scholar] [CrossRef] [Green Version]
  104. Pilon, G.; Dallaire, P.; Marette, A. Inhibition of inducible nitric-oxide synthase by activators of AMP-activated protein kinase: A new mechanism of action of insulin-sensitizing drugs. J. Biol. Chem. 2004, 279, 20767–20774. [Google Scholar] [CrossRef] [Green Version]
  105. Nath, N.; Giri, S.; Prasad, R.; Salem, M.L.; Singh, A.K.; Singh, I. 5-aminoimidazole-4-carboxamide ribonucleoside: A novel immunomodulator with therapeutic efficacy in experimental autoimmune encephalomyelitis. J. Immunol. 2005, 175, 566–574. [Google Scholar] [CrossRef] [Green Version]
  106. McFaul, S.J.; Corley, J.B.; Mester, C.W.; Nath, J. Packed blood cells stored in AS-5 become proinflammatory during storage. Transfusion 2009, 49, 1451–1460. [Google Scholar] [CrossRef]
  107. Chen, G.; Feng, W.; Zhang, S.; Bian, K.; Yang, Y.; Fang, C.; Chen, M.; Yang, J.; Zou, X. Metformin inhibits gastric cancer via the inhibition of HIF1alpha/PKM2 signaling. Am. J. Cancer Res. 2015, 5, 1423–1434. [Google Scholar]
  108. Zhang, Y.; Qiu, J.; Wang, X.; Zhang, Y.; Xia, M. AMP-activated protein kinase suppresses endothelial cell inflammation through phosphorylation of transcriptional coactivator p300. Arterioscler. Thromb. Vasc. Biol 2011, 31, 2897–2908. [Google Scholar] [CrossRef] [Green Version]
  109. Vaez, H.; Rameshrad, M.; Najafi, M.; Barar, J.; Barzegari, A.; Garjani, A. Cardioprotective effect of metformin in lipopolysaccharide-induced sepsis via suppression of toll-like receptor 4 (TLR4) in heart. Eur. J. Pharmacol. 2016, 772, 115–123. [Google Scholar] [CrossRef]
Antioxidants 09 00525 g001 550
Figure 1. Physiological functions of the vascular adenosine monophosphate-activated protein kinase (AMPK). Activation of the vascular AMPK leads to enhanced platelet activation and thrombus stabilization, beneficial impact on the vascular function by eNOS phosphorylation and reduction of oxidative stress by controlling mitochondrial biogenesis and mitochondrial gene expression. Furthermore, it is known that inflammatory processes as well as the recruitment of inflammatory cells into the vascular wall are regulated by AMPK. In this context, AMPK is able to promote angiogenesis, reducing endothelial cell apoptosis and inhibiting smooth muscle cell proliferation. The most recent data points to functions of AMPK regulating the posttranslational modulation of histones leading to changes in epigenetic regulation of gene expression. Abbreviations: AMPK: adenosine monophosphate-activated protein kinase; AT II: angiotensin II; eNOS: endothelial nitric oxide synthase; H2O2: hydrogen peroxide; ONOO−: peroxynitrite anion; PGC-1α: peroxisome proliferator-activated receptor gamma coactivator 1-alpha; SIRT-1: sirtuin 1; SMC: smooth muscle cell.
Figure 1. Physiological functions of the vascular adenosine monophosphate-activated protein kinase (AMPK). Activation of the vascular AMPK leads to enhanced platelet activation and thrombus stabilization, beneficial impact on the vascular function by eNOS phosphorylation and reduction of oxidative stress by controlling mitochondrial biogenesis and mitochondrial gene expression. Furthermore, it is known that inflammatory processes as well as the recruitment of inflammatory cells into the vascular wall are regulated by AMPK. In this context, AMPK is able to promote angiogenesis, reducing endothelial cell apoptosis and inhibiting smooth muscle cell proliferation. The most recent data points to functions of AMPK regulating the posttranslational modulation of histones leading to changes in epigenetic regulation of gene expression. Abbreviations: AMPK: adenosine monophosphate-activated protein kinase; AT II: angiotensin II; eNOS: endothelial nitric oxide synthase; H2O2: hydrogen peroxide; ONOO−: peroxynitrite anion; PGC-1α: peroxisome proliferator-activated receptor gamma coactivator 1-alpha; SIRT-1: sirtuin 1; SMC: smooth muscle cell.
Antioxidants 09 00525 g001
Antioxidants 09 00525 g002 550
Figure 2. Structure and regulation of heterotrimeric AMPK. The model was created with MacPyMol using protein database (PDB) file 4CFE. The α, β and γ subunits are shown in “cartoon view” with domains color-coded. The three bound molecules of AMP, and phospho-Thr172 are shown in “sphere view” with C atoms green, O red, N blue and P orange. The different classes of compounds and their specific points of action are listed in green. Abbreviations: AICAR: 5-aminoimidazole-4-carboxymide ribonucleoside; AID: autoinhibitory domain; AMP: adenosine monophosphate; AMPK: adenosine monophosphate protein kinase; CaMKK: calmodulin-dependent kinase kinases; CBM: carbohydrate-binding module; C13: compound 13; LKB1: liver kinase B1; TAK1: transforming growth factor-β-activated kinase 1; Thr: threonin; adopted from [59] with permission. Copyright © 2014 Elsevier Inc. All rights reserved.
Figure 2. Structure and regulation of heterotrimeric AMPK. The model was created with MacPyMol using protein database (PDB) file 4CFE. The α, β and γ subunits are shown in “cartoon view” with domains color-coded. The three bound molecules of AMP, and phospho-Thr172 are shown in “sphere view” with C atoms green, O red, N blue and P orange. The different classes of compounds and their specific points of action are listed in green. Abbreviations: AICAR: 5-aminoimidazole-4-carboxymide ribonucleoside; AID: autoinhibitory domain; AMP: adenosine monophosphate; AMPK: adenosine monophosphate protein kinase; CaMKK: calmodulin-dependent kinase kinases; CBM: carbohydrate-binding module; C13: compound 13; LKB1: liver kinase B1; TAK1: transforming growth factor-β-activated kinase 1; Thr: threonin; adopted from [59] with permission. Copyright © 2014 Elsevier Inc. All rights reserved.
Antioxidants 09 00525 g002
Antioxidants 09 00525 g003 550
Figure 3. Functions of endothelial specific α1AMPK. (A,B) Epifluorescence intravital microscopy was used to visualize adherent and rolling leucocytes in carotid arteries. Nucleated cells were stained with acridine orange (green fluorescence). Representative images of carotid arteries are shown after 7 days of continuous AT II infusion (n = 8) before and 60 min after single intraperitoneal injection of anti-CCR2 antibody (anti-CCR2). Deletion of endothelial-specific α1AMPK (AMPKfl/fl×CadhCre+ + AT II) leads to a loss of endothelial barrier function and an enormous AT II-induced increase in CCR-2-dependent recruitment of inflammatory cells to the vascular wall in comparison with the wild-type littermates (CadhCre+ + AT II) that was prevented by anti-CCR2 treatment. * p < 0.05 vs. CadhCre+ + AT II, ** p < 0.05 vs. AMPKfl/fl×CadhCre+ + AT II. (C) mRNA expression of MCP-1 was significantly upregulated in aortic tissue of AT II-treated mice lacking α1AMPK in the endothelium (n = 6), which was accompanied by immune cell infiltration and (D) increased NOX-2 protein measured by immunohistochemistry (brown staining) (n = 4). (E) Furthermore, oxidative stress, measured by Amplex Red assay (n = 4), was significantly increased in mice lacking the endothelial α1AMPK treated with AT II. (F) In addition to this, the loss of endothelial α1AMPK impaired the antioxidant defense induced normally by AT II (n = 11). * p < 0.05 vs. WT CTL, ** p < 0.05 vs. WT AngII, # p < 0.05 vs. AMPK EC KO CTL. Data were reused from [94] with permission. Copyright © 2019, Springer-Verlag GmbH Germany, part of Springer Nature. Abbreviations: AMPK EC KO: TekCre-specific AMPK deletion (AMPKfl/flxTekCre+); AMPK: adenosine monophosphate-activated protein kinase; AT II: angiotensin II; CCR-2: C-C motif chemokine receptor 2; HO-1: heme oxygenase-1; H2O2: hydrogen peroxide; NOX-2: nicotinamide adenine dinucleotide phosphate oxidase 2; MCP-1: monocyte chemoattractant protein-1.
Figure 3. Functions of endothelial specific α1AMPK. (A,B) Epifluorescence intravital microscopy was used to visualize adherent and rolling leucocytes in carotid arteries. Nucleated cells were stained with acridine orange (green fluorescence). Representative images of carotid arteries are shown after 7 days of continuous AT II infusion (n = 8) before and 60 min after single intraperitoneal injection of anti-CCR2 antibody (anti-CCR2). Deletion of endothelial-specific α1AMPK (AMPKfl/fl×CadhCre+ + AT II) leads to a loss of endothelial barrier function and an enormous AT II-induced increase in CCR-2-dependent recruitment of inflammatory cells to the vascular wall in comparison with the wild-type littermates (CadhCre+ + AT II) that was prevented by anti-CCR2 treatment. * p < 0.05 vs. CadhCre+ + AT II, ** p < 0.05 vs. AMPKfl/fl×CadhCre+ + AT II. (C) mRNA expression of MCP-1 was significantly upregulated in aortic tissue of AT II-treated mice lacking α1AMPK in the endothelium (n = 6), which was accompanied by immune cell infiltration and (D) increased NOX-2 protein measured by immunohistochemistry (brown staining) (n = 4). (E) Furthermore, oxidative stress, measured by Amplex Red assay (n = 4), was significantly increased in mice lacking the endothelial α1AMPK treated with AT II. (F) In addition to this, the loss of endothelial α1AMPK impaired the antioxidant defense induced normally by AT II (n = 11). * p < 0.05 vs. WT CTL, ** p < 0.05 vs. WT AngII, # p < 0.05 vs. AMPK EC KO CTL. Data were reused from [94] with permission. Copyright © 2019, Springer-Verlag GmbH Germany, part of Springer Nature. Abbreviations: AMPK EC KO: TekCre-specific AMPK deletion (AMPKfl/flxTekCre+); AMPK: adenosine monophosphate-activated protein kinase; AT II: angiotensin II; CCR-2: C-C motif chemokine receptor 2; HO-1: heme oxygenase-1; H2O2: hydrogen peroxide; NOX-2: nicotinamide adenine dinucleotide phosphate oxidase 2; MCP-1: monocyte chemoattractant protein-1.
Antioxidants 09 00525 g003
Antioxidants 09 00525 g004 550
Figure 4. Functions of monocyte-specific α1AMPK. (A) Endothelial-dependent relaxation in response to acetylcholine was analyzed by isometric tension studies in intact aortic rings from myelomonocytic cell-specific α1AMPK knockout mice (α1AMPKfl/fl LysM-Cre) and corresponding wild-type littermates (LysMCre/wt) treated with AT II (1.0 mg/kg for 7 days; n = 8–10 mice/group). (B) Phorbolester (PDBu)-stimulated oxidative burst in whole blood was determined by L-012-enhanced chemiluminescence (n = 12). * p <0.05 vs LysMCre+ CTL, § p <0.05 vs. AMPKfl/fl x LysMCre+, # p <0.05 vs. LysMCre+ + AT II. (C) Epifluorescence intravital microscopy was used to visualize adherent and rolling leucocytes in carotid arteries. Nucleated cells were stained with acridine orange (green fluorescence). Representative images of carotid arteries after 7 days of continuous AT II infusion (n = 8), before and 60 min after single intraperitoneal injection of anti-CCR2 antibody (CCR2ab). (D) Pro inflammatory cytokine level of IFN-γ was measured by real-time PCR (n = 10). Data were reused from [103] with permission. Copyright © 2018, Oxford University Press. Abbreviations: AMPK: adenosine monophosphate-activated protein kinase; AT II: angiotensin II; CCR-2: C-C motif chemokine receptor 2.
Figure 4. Functions of monocyte-specific α1AMPK. (A) Endothelial-dependent relaxation in response to acetylcholine was analyzed by isometric tension studies in intact aortic rings from myelomonocytic cell-specific α1AMPK knockout mice (α1AMPKfl/fl LysM-Cre) and corresponding wild-type littermates (LysMCre/wt) treated with AT II (1.0 mg/kg for 7 days; n = 8–10 mice/group). (B) Phorbolester (PDBu)-stimulated oxidative burst in whole blood was determined by L-012-enhanced chemiluminescence (n = 12). * p <0.05 vs LysMCre+ CTL, § p <0.05 vs. AMPKfl/fl x LysMCre+, # p <0.05 vs. LysMCre+ + AT II. (C) Epifluorescence intravital microscopy was used to visualize adherent and rolling leucocytes in carotid arteries. Nucleated cells were stained with acridine orange (green fluorescence). Representative images of carotid arteries after 7 days of continuous AT II infusion (n = 8), before and 60 min after single intraperitoneal injection of anti-CCR2 antibody (CCR2ab). (D) Pro inflammatory cytokine level of IFN-γ was measured by real-time PCR (n = 10). Data were reused from [103] with permission. Copyright © 2018, Oxford University Press. Abbreviations: AMPK: adenosine monophosphate-activated protein kinase; AT II: angiotensin II; CCR-2: C-C motif chemokine receptor 2.
Antioxidants 09 00525 g004
Antioxidants 09 00525 g005 550
Figure 5. Inflammatory responses on myelomonocytic- and endothelial-specific α1AMPK knockout cells. Loss of myelomonocytic (LysMCre)-specific α1AMPK affects vascular and whole blood oxidative stress and endothelial function by regulating the recruitment of inflammatory cells (enhancement of CCR-2, MCP-1 and other recruiting molecules) to the vascular wall and higher white blood cell (WBC) activation state (reflected by WBC oxidative burst). This also promotes an increase in angiotensin II receptor type 1, leading to higher responsiveness towards pro-oxidant stimuli and in conclusion a pro-inflammatory phenotype (IL-6, TNFα, IFNγ upregulation). Loss of endothelial-specific α1AMPK impairs the endothelial barrier function, resulting in an increased CCR-2/MCP-1 (recruiting molecules)-mediated infiltration of inflammatory cells. This situation provokes an overproduction of reactive oxygen species, leading to oxidative tissue damage and vascular inflammation. Furthermore, deletion of endothelial-specific α1AMPK disables the antioxidant system by blunting HO-1 induction. Abbreviations: AMPK: adenosine monophosphate-activated protein kinase; AT II: angiotensin II; AT1R: angiotensin II receptor type 1; CCR-2: C-C motif chemokine receptor 2; HO-1: heme oxygenase-1; WBC: white blood cell.
Figure 5. Inflammatory responses on myelomonocytic- and endothelial-specific α1AMPK knockout cells. Loss of myelomonocytic (LysMCre)-specific α1AMPK affects vascular and whole blood oxidative stress and endothelial function by regulating the recruitment of inflammatory cells (enhancement of CCR-2, MCP-1 and other recruiting molecules) to the vascular wall and higher white blood cell (WBC) activation state (reflected by WBC oxidative burst). This also promotes an increase in angiotensin II receptor type 1, leading to higher responsiveness towards pro-oxidant stimuli and in conclusion a pro-inflammatory phenotype (IL-6, TNFα, IFNγ upregulation). Loss of endothelial-specific α1AMPK impairs the endothelial barrier function, resulting in an increased CCR-2/MCP-1 (recruiting molecules)-mediated infiltration of inflammatory cells. This situation provokes an overproduction of reactive oxygen species, leading to oxidative tissue damage and vascular inflammation. Furthermore, deletion of endothelial-specific α1AMPK disables the antioxidant system by blunting HO-1 induction. Abbreviations: AMPK: adenosine monophosphate-activated protein kinase; AT II: angiotensin II; AT1R: angiotensin II receptor type 1; CCR-2: C-C motif chemokine receptor 2; HO-1: heme oxygenase-1; WBC: white blood cell.
Antioxidants 09 00525 g005

Share and Cite

MDPI and ACS Style

Jansen, T.; Kvandová, M.; Daiber, A.; Stamm, P.; Frenis, K.; Schulz, E.; Münzel, T.; Kröller-Schön, S. The AMP-Activated Protein Kinase Plays a Role in Antioxidant Defense and Regulation of Vascular Inflammation. Antioxidants 2020, 9, 525. https://doi.org/10.3390/antiox9060525

AMA Style

Jansen T, Kvandová M, Daiber A, Stamm P, Frenis K, Schulz E, Münzel T, Kröller-Schön S. The AMP-Activated Protein Kinase Plays a Role in Antioxidant Defense and Regulation of Vascular Inflammation. Antioxidants. 2020; 9(6):525. https://doi.org/10.3390/antiox9060525

Chicago/Turabian Style

Jansen, Thomas, Miroslava Kvandová, Andreas Daiber, Paul Stamm, Katie Frenis, Eberhard Schulz, Thomas Münzel, and Swenja Kröller-Schön. 2020. "The AMP-Activated Protein Kinase Plays a Role in Antioxidant Defense and Regulation of Vascular Inflammation" Antioxidants 9, no. 6: 525. https://doi.org/10.3390/antiox9060525

APA Style

Jansen, T., Kvandová, M., Daiber, A., Stamm, P., Frenis, K., Schulz, E., Münzel, T., & Kröller-Schön, S. (2020). The AMP-Activated Protein Kinase Plays a Role in Antioxidant Defense and Regulation of Vascular Inflammation. Antioxidants, 9(6), 525. https://doi.org/10.3390/antiox9060525

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop