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Authors = Xiaoliang Li

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XIAOLIANG (33) , LI (9285)

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Open AccessArticle Porcine Circovirus Type 2 Activates CaMMKβ to Initiate Autophagy in PK-15 Cells by Increasing Cytosolic Calcium
Viruses 2016, 8(5), 135; doi:10.3390/v8050135
Received: 12 March 2016 / Revised: 11 May 2016 / Accepted: 12 May 2016 / Published: 20 May 2016
Cited by 3 | Viewed by 923 | PDF Full-text (4320 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
Porcine circovirus type 2 (PCV2) induces autophagy via the 5′ adenosine monophosphate-activated protein kinase (AMPK)/extracellular signal-regulated kinase (ERK)/tuberous sclerosis complex 2 (TSC2)/mammalian target of rapamycin (mTOR) pathway in pig kidney PK-15 cells. However, the underlying mechanisms of AMPK activation in autophagy induction remain
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Porcine circovirus type 2 (PCV2) induces autophagy via the 5′ adenosine monophosphate-activated protein kinase (AMPK)/extracellular signal-regulated kinase (ERK)/tuberous sclerosis complex 2 (TSC2)/mammalian target of rapamycin (mTOR) pathway in pig kidney PK-15 cells. However, the underlying mechanisms of AMPK activation in autophagy induction remain unknown. With specific inhibitors and RNA interference (RNAi), we show that PCV2 infection upregulated calcium/calmodulin-dependent protein kinase kinase-beta (CaMKKβ) by increasing cytosolic Ca2+ via inositol 1,4,5-trisphosphate receptor (IP3R). Elevation of cytosolic calcium ion (Ca2+) did not seem to involve inositol 1,4,5-trisphosphate (IP3) release from phosphatidylinositol 4,5-bisphosphate (PIP2) by phosphoinositide phospholipase C-gamma (PLC-γ). CaMKKβ then activated both AMPK and calcium/calmodulin-dependent protein kinase I (CaMKI). PCV2 employed CaMKI and Trp-Asp (WD) repeat domain phosphoinositide-interacting protein 1 (WIPI1) as another pathway additional to AMPK signaling in autophagy initiation. Our findings could help better understanding of the signaling pathways of autophagy induction as part of PCV2 pathogenesis. Further research is warranted to study if PCV2 interacts directly with IP3R or indirectly with the molecules that antagonize IP3R activity responsible for increased cytosolic Ca2+ both in PK-15 cells and PCV2-targeted primary cells from pigs. Full article
(This article belongs to the Section Animal Viruses)
Open AccessArticle Identification and Functional Analysis of Interleukin-1β in the Chinese Soft-Shelled Turtle Pelodiscus sinensis
Genes 2016, 7(5), 18; doi:10.3390/genes7050018
Received: 22 March 2016 / Revised: 25 April 2016 / Accepted: 27 April 2016 / Published: 4 May 2016
Viewed by 766 | PDF Full-text (3481 KB) | HTML Full-text | XML Full-text | Supplementary Files
Abstract
Chinese soft-shelled turtle (Pelodiscus sinensis) is commercially cultured in East and Southeast Asia for its nutritional and medicinal values. In this study, we identified interleukin-1β (IL-1β) from Chinese soft-shelled turtle. The full-length cDNA of Pelodiscus sinensis IL-1β (tIL-1β) consists of 1529
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Chinese soft-shelled turtle (Pelodiscus sinensis) is commercially cultured in East and Southeast Asia for its nutritional and medicinal values. In this study, we identified interleukin-1β (IL-1β) from Chinese soft-shelled turtle. The full-length cDNA of Pelodiscus sinensis IL-1β (tIL-1β) consists of 1529 base pairs with an 831-base-pair open reading frame, encoding 277 amino acids. The guanine-cytosine (GC) content in the coding sequence and 3’ untranslated region of tIL-1β is considerably higher than that of other vertebrates. Its mRNA expression level increased significantly during Aeromonas hydrophila infection. The tIL-1β lacks the typical IL-1β-converting enzyme (ICE) cut site found in mammalian IL-1β, but still could be cleaved by turtle caspase-1. By mutating the potential cleavage sites, we identified aspartic acid (Asp/D) 130 as the ICE cut site in tIL-1β. The peptide truncated at D130 was expressed using the baculovirus expression system; its bioactivity is confirmed by the ability to induce cyclooxygenase-2 (COX-2) and tIL-1β itself in peripheral blood monocytes. In conclusion, we characterized IL-1β from Chinese soft-shelled turtle and identified its D130 as a non-typical ICE cut size. Full article
(This article belongs to the Section Molecular Genetics)
Open AccessArticle Porcine Circovirus 2 Deploys PERK Pathway and GRP78 for Its Enhanced Replication in PK-15 Cells
Viruses 2016, 8(2), 56; doi:10.3390/v8020056
Received: 3 November 2015 / Revised: 6 February 2016 / Accepted: 17 February 2016 / Published: 20 February 2016
Cited by 2 | Viewed by 1263 | PDF Full-text (4001 KB) | HTML Full-text | XML Full-text
Abstract
Porcine circovirus type 2 (PCV2) infection induces autophagy and apoptosis. These cellular responses could be connected with endoplasmic reticulum (ER) stress. It remains unknown if PCV2 induces ER stress and if autophagy or apoptosis is primary to PCV2 infection or secondary responses following
[...] Read more.
Porcine circovirus type 2 (PCV2) infection induces autophagy and apoptosis. These cellular responses could be connected with endoplasmic reticulum (ER) stress. It remains unknown if PCV2 induces ER stress and if autophagy or apoptosis is primary to PCV2 infection or secondary responses following ER stress. Here, we demonstrate that PCV2 triggered unfolded protein response (UPR) in PK-15 cells by activating the PERK/eIF2α pathway without concomitant activation of IRE1 or ATF6. Since ATF4 and CHOP were induced later than PERK/eIF2α, it is clear that persistent PCV2 infection could lead to selective activation of PERK via the PERK-eIF2α-ATF4-CHOP axis. Therefore, PERK activation could be part of the pro-apoptotic signaling via induced expression of CHOP by PCV2. Since PERK inhibition by GSK2606414 or RNA silencing or suppression of eIF2α dephosphorylation by salubrinal limited viral replication, we suppose that PCV2 deploys UPR to enhance its replication. Over-expression of GRP78 or treatment with tauroursodeoxycholic acid could enhance viral capsid expression and/or viral titers, indicating that these chaperones, endogenous or exogenous, could help correct folding of viral proteins. Our findings provide the first evidence that ER stress plays a role in the pathogenesis of PCV2 infection probably as part of autophagic and apoptotic responses. Full article
(This article belongs to the Section Animal Viruses)
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Open AccessArticle A Magnetic Nanoparticle Based Enzyme-Linked Immunosorbent Assay for Sensitive Quantification of Zearalenone in Cereal and Feed Samples
Toxins 2015, 7(10), 4216-4231; doi:10.3390/toxins7104216
Received: 11 September 2015 / Revised: 6 October 2015 / Accepted: 13 October 2015 / Published: 20 October 2015
Cited by 6 | Viewed by 1153 | PDF Full-text (698 KB) | HTML Full-text | XML Full-text
Abstract
A novel enzyme-linked immunosorbent assay based on magnetic nanoparticles and biotin/streptavidin-HRP (MNP-bsELISA) was developed for rapid and sensitive detection of zearalenone (ZEN). The detection signal was enhanced and the sensitivity of the assay was improved by combined use of antibody-conjugated magnetic nanoparticles and
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A novel enzyme-linked immunosorbent assay based on magnetic nanoparticles and biotin/streptavidin-HRP (MNP-bsELISA) was developed for rapid and sensitive detection of zearalenone (ZEN). The detection signal was enhanced and the sensitivity of the assay was improved by combined use of antibody-conjugated magnetic nanoparticles and biotin-streptavidin system. Under the optimized conditions, the regression equation for quantification of ZEN was y = −0.4287x + 0.3132 (R2 = 0.9904). The working range was 0.07–2.41 ng/mL. The detection limit was 0.04 ng/mL and IC50 was 0.37 ng/mL. The recovery rates of intra-assay and inter-assay ranged from 92.8%–111.9% and 91.7%–114.5%, respectively, in spiked corn samples. Coefficients of variation were less than 10% in both cases. Parallel analysis of cereal and feed samples showed good correlation between MNP-bsELISA and liquid chromatograph-tandem mass spectrometry (R2 = 0.9283). We conclude that this method is suitable for rapid detection of zearalenone in cereal and feed samples in relevant laboratories. Full article
(This article belongs to the collection Biorecognition Assays for Mycotoxins)
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Open AccessArticle Design and Implementation of a High Quality Power Supply Scheme for Distributed Generation in a Micro-Grid
Energies 2013, 6(9), 4924-4944; doi:10.3390/en6094924
Received: 23 July 2013 / Revised: 12 September 2013 / Accepted: 17 September 2013 / Published: 23 September 2013
Cited by 10 | Viewed by 2453 | PDF Full-text (677 KB) | HTML Full-text | XML Full-text
Abstract
A low carbon, high efficiency and high quality power supply scheme for Distributed Generation (DG) in a micro-grid is presented. A three-phase, four-leg DG grid-interfacing converter based on the improved structure of a Unified Power Quality Conditioner (UPQC, including a series converter and
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A low carbon, high efficiency and high quality power supply scheme for Distributed Generation (DG) in a micro-grid is presented. A three-phase, four-leg DG grid-interfacing converter based on the improved structure of a Unified Power Quality Conditioner (UPQC, including a series converter and a parallel converter) is adopted, and improved indirect and direct control strategies are proposed. It can be observed that these strategies effectively compensate for voltage sags, voltage swells and voltage distortion, as well as voltage power quality problems resulting from the nonlinear and unbalanced loads in a micro-grid. While solving the coupling interference from series–parallel, the grid-interfacing converter can achieve proper load power sharing in a micro-grid. In particular, an improved minimum-energy compensation method is proposed that can overcome the conventional compensation algorithm defects, ensure the load voltage’s phase angle stability, improve the voltage compensating ability and range, reduce the capacity and cost of converters, and reduce the shock of micro-grid switching between grid-connected mode and islanded mode. Moreover, the advantages/disadvantages and application situation of the two improved control strategies are analyzed. Finally, the performance of the proposed control strategies has been verified through a MATLAB/Simulink simulation under various operating conditions. Full article
(This article belongs to the Special Issue Smart Grids: The Electrical Power Network and Communication System)

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