Search Results (650)

With the continuous development of China’s economy and technology, the number of urban transportation shield tunnels has been increasing. As tunnel depth and diameter grow, the geological conditions become increasingly complex, making leakage at segment joints of shield tunnels a more prominent issue, significantly affecting the sustainable development of urban transportation. To address the issue of water leakage, microbially induced calcium carbonate precipitation (MICP) technology offers a green and environmentally friendly solution. However, relying solely on MICP technology is insufficient to enhance the waterproofing performance of large segment joints of shield tunnel. To address this, this study proposes combining diatomite as both a carrier and filler material with MICP technology, using a diatomite–MICP composite grout to improve the waterproofing performance of tunnel segment joints. First, through laboratory macro-scale tests and micro-morphology analysis, the influence of diatomite dosage on the sealing performance of diatomite–MICP composite grout was systematically studied, and the optimal diatomite dosage was determined. Based on this, a self-developed segment joint waterproofing testing platform was adopted to conduct hydraulic tests on double-seal gasket joints, evaluating the enhancement effect of the composite grout on the overall waterproofing performance of tunnel segment joints. The results indicated that the dosage of diatomite significantly affects the sealing performance of the composite grout, with an optimal dosage of 20% by weight of the bacterial solution. At this dosage, the composite grout achieved the highest density, resulting in maximum unconfined compressive strength and shear strength, as well as the lowest permeability coefficient. The joint water pressure test confirmed that after grouting with a diatomite–MICP composite grout at the optimal dosage of 20%, the breakdown water pressures of the inner and outer seal gaskets at the segment joints reached 2011 kPa and 2019 kPa, representing increases of 15.91% and 16.64% compared to the control group without grouting. This study demonstrates the effectiveness and application potential of the green biomineralization technologies in waterproofing of shield tunnel joints. Full article

Solute carrier family 25 (SLC25) is known to facilitate the transport of diverse metabolites across the mitochondrial and peroxisomal membranes. SLC25A17 is the only member of the SLC25 protein localized to peroxisomes; formerly known as PMP34, it also shares conserved sequence features with other SLC families. SLC25A17 was first described as an ATP transporter, but conflicting results regarding cofactor specificity in various experimental models obscure its precise function. Similarly, phenotypic differences between experimental models, such as mice and zebrafish, complicate the application of animal studies to humans. In particular, SLC25A17 deficiency is associated with peroxisomal dysfunction, and SLC25A17 expression is affected in various cancers and bipolar disorder, while the underlying molecular mechanisms remain unknown. Furthermore, it remains unclear whether altered SLC25A17 expression is a cause or consequence of human disease. This review provides an overview on current knowledge of SLC25A17, focusing on its known functions and emerging roles in human diseases. This may also help future studies in understanding its metabolic significance and disease pathogenesis. Full article

Natural gas transportation and distribution networks are becoming increasingly heterogeneous due to the injection of biomethane, regasified LNG, and hydrogen-enriched natural gas, requiring distributed and continuous gas-quality monitoring. This work presents an industrial Raman-based instrument for in-line measurement of natural gas and hydrogen-enriched natural gas composition and related thermodynamic properties. The system employs a 450 nm broadband laser diode, a high-throughput custom spectrometer, and a pressure-rated gas cell integrated in an ATEX-certified enclosure. Gas composition is retrieved through calibration spectra and non-linear least-squares fitting, while higher heating value is calculated according to ISO 6976. The instrument was validated over pressures from 1.5 to 17 bara and temperatures from −20 °C to 55 °C using certified representative gas mixtures. The system achieved compliance with OIML R 140 Class A requirements, with HHV errors below ±0.5% and repeatability within 0.1%, while operating without carrier gases or sample manipulation. Long-term field operations in pressure-reduction stations confirmed stable performance over twelve months. The results demonstrate that Raman spectroscopy can provide a robust, low-maintenance solution for continuous natural-gas-quality monitoring and controlled hydrogen-blending applications. Full article

This study investigates the application of polymer inclusion membranes (PIMs) for the removal/recovery of 1H-benzotriazole from aqueous solutions, via facilitated transport mechanism, using tri-n-octylamine as a carrier and NaOH as a stripping agent. The process efficiency was analyzed using 1H-benzotriazole flux and permeability through the membrane, its recovery percentage, and the transport process kinetic constant. PIM containing 40% cellulose triacetate, 30% o-nitrophenyl octyl ether and 30% tri-n-octylamine yielded the best results for all four parameters studied due to the role of o-nitrophenyl octyl ether and tri-n-octylamine in reducing the cellulose triacetate polarity, which leads to carrier solubilization on the plasticizer, creating continuous pathways within the membrane and facilitating 1H-benzotriazole transport. Reduced graphene oxide inclusion as the fourth PIM component increases its hydrophobicity, promoting continuous pathway formation and enhancing 1H-benzotriazole transport, which leads to an increase of 10% to 20% in the values of the four parameters analyzed. Ultrasound use in membrane preparation leads to a further increase of 9% to 20% in the values of the four parameters analyzed because the cavitation effect improves the molecular mixing of membrane components and results in a less ordered configuration of cellulose triacetate molecules, thereby reducing their crystallinity degree. All of this significantly improves the interaction between the membrane components and pathway formation, enhancing 1H-benzotriazole transport through the membrane. Full article

Neurodegenerative diseases are increasingly recognized as disorders of due to disrupted cellular homeostasis, with mitochondrial dysfunction playing a central and early role in disease progression. This review explores the intricate relationship between mitochondrial function and neuronal health, emphasizing the pivotal role of the solute carrier family 25 (SLC25) transporters in maintaining mitochondrial homeostasis. We provide a comprehensive overview of mitochondrial biology in the central nervous system, including energy metabolism, calcium signaling, redox regulation, organelle interactions and mitochondrial dynamics. We delve into the SLC25 transporter family, highlighting their transport mechanisms, substrates and roles in brain metabolism and neuroprotection. SLC25 on one hand and proteins involved in the regulation of mitochondrial morphology and calcium signaling on the other hand are two sides of the same coin influencing each other. A critical analysis follows, examining how mitochondrial dysfunction contributes to mitochondrial abnormalities in a spectrum of neurodegenerative diseases, including Alzheimer’s disease, Parkinson’s disease, ALS and rare mitochondrial encephalopathies. Finally, we assess emerging therapeutic strategies targeting mitochondrial pathways and SLC25 function, including metabolic modulation, gene therapies, antioxidants and pharmacological agents. This review underscores mitochondria and the SLC25 transporters as promising targets for disease-modifying interventions in neurodegeneration and raises key questions about the causality between mitochondrial failure and neuronal death. Full article

Background/Objectives: The gene solute carrier family 52 member 3 (SLC52A3) encodes riboflavin transporter-3, a transmembrane protein essential for riboflavin absorption. Emerging evidence suggests that metabolic transporters may play a role in tumor biology. This study aimed to investigate the expression patterns, prognostic significance, genetic alterations, and functional associations of SLC52A3 in gynecological cancers. Methods: A comprehensive bioinformatic analysis was conducted using multi-omics datasets from The Cancer Genome Atlas (TCGA). Gene expression and survival analyses were performed via GEPIA3. Genetic alterations, including mutations and copy number variations, were assessed using cBioPortal. Immune infiltration correlations were analyzed through TIMER3. Protein–protein interactions and gene enrichment analyses were performed using STRING and GEPIA2, followed by Gene Ontology (GO) and KEGG pathway analyses. Results: SLC52A3 expression was significantly upregulated in ovarian, cervical, and endometrial cancers. Reduced expression of SLC52A3 was associated with poorer overall survival and shorter progression-free interval specifically in endometrial cancer. Genetic alterations in SLC52A3 were not significantly associated with survival outcomes (OS, DFS, and PFS). Functional enrichment analysis indicated that SLC52A3 is involved in biological processes such as cell junction organization and protein localization to the plasma membrane. Additionally, SLC52A3 expression showed positive correlations with genes implicated in tumor progression and metastasis, including NECTIN4, PROM2, TACSTD2, PKP3, SEMA4B, and CD46. Conclusions: These findings suggest that SLC52A3 may serve as a potential prognostic biomarker in endometrial cancer and could play a role in tumor progression pathways. Its functional associations highlight its potential relevance as a therapeutic target, warranting further experimental validation. Full article

Epidemiological and biological evidence indicate a close connection between Alzheimer’s disease (AD) and type-2 diabetes mellitus. Glucose transporter 1 (GLUT1), encoded by the SLC2A1 gene, has a major role in glucose metabolism, the dysregulation of which has been implicated in both diseases. We conducted a case-control association study in a sample of 439 non-diabetic patients with late-onset AD and 304 cognitively healthy, non-diabetic elderly controls to determine the potential risk for developing AD associated with SLC2A1 rs841847 polymorphism. The rs841847 C/C genotype occurrence was higher in the AD group (AD: 60.4%, controls: 50.7%), while the minor T allele-containing genotypes were more frequent among controls (AD: 39.6%, controls: 49.3%). A multivariate logistic regression model adjusted for age, sex, and apolipoprotein E (APOE) ε4 status (ε4 allele carriers versus non-carriers) demonstrated that carriers of the T allele had a significantly reduced risk for AD compared to C/C homozygotes (OR = 0.672; 95% CI: 0.493–0.916; p = 0.012). Although the rs841847 polymorphism has been linked to type-2 diabetes mellitus, the present study investigated this gene variant in AD for the first time. Our findings indicate a moderate protective effect for the rs841847 T allele on the susceptibility to AD. We demonstrated the rs841847 polymorphism as a candidate single nucleotide polymorphism for further examination as a predisposing genetic factor for AD. Full article

Background: The regulation of inorganic phosphate (Pi) homeostasis is predominantly mediated by the Pi transporters belonging to the SLC34 and SLC20 families of solute carriers. However, not all Pi handling can be explained by these transporters. In this study, we sought to identify novel Pi transporters in accordance with prior findings on inhibition patterns. Methods: We have performed a functional screening of new Pi carriers using the Xenopus laevis oocyte expression system, focusing on the SLC26 family, and corroboration in cell culture. Results: Both SLC26A7 and SLC26A9 have been shown to express sodium-activated Pi uptakes with approximately 200 µmol/L Pi affinity. In both cases, Pi transport is inhibited by increasing pH and by phosphonoformate, arsenate, bicarbonate, sulfate, the chloride channel inhibitor 5-nitro-2-[(3-phenylpropyl)amino]-benzoate, and several transport site and translocation inhibitors of bicarbonate exchangers. In addition, the CFTR inhibitor GlyH-101 and the SLC4 inhibitors DIDS, SITS, and phloretin exhibited partial inhibition of SLC26A9-mediated Pi uptake. The endogenous expressions of both SLC26A7 and SLC26A9 in the renal cell lines LLC-PK1 and MDCK were primarily intracellular, colocalizing with endosomes, lysosomes, and the trans-Golgi network markers. Conversely, plasma membrane expression was found to be minimal. Pi transport in MDCK cells was sodium-independent, but when either SLC26A7 or SLC26A9 was overexpressed, sodium-activated Pi uptake was observed, along with increased expressions of SLC26A7 or SLC26A9 in the plasma membrane. Conclusions: Sodium-activated Pi transport is a novel function of the SLC26A7 and SLC26A9 multifunctional anion transporters. Further research is necessary to ascertain the relevance to Pi homeostasis in vivo. Full article

Background/Objectives: Lactobacillus rhamnosus GG (LGG) is one of the most widely utilized probiotic strains with a variety of biological functions including prevention and treatment of gastro-intestinal infections and regulation of immune responses. Methods: Here, we explored the role of LGG in regulating the differentiation of naïve CD4⁺ T cells and its effect on alleviating the dextran sulfate sodium (DSS)-induced colitis in mice. Results: In vitro, we showed that LGG-derived metabolites not only promoted the differentiation of naive CD4⁺ T cells into T-helper 17 cells (Th17 cells), but also selectively upregulated the expression of lactate-specific transporter solute carrier family 5 member 12 (SLC5A12). Interestingly, we manipulated a CD4⁺ T cell-monocytes co-culture and found that heated LGG-loaded monocytes modulate naive CD4⁺ T cells to differentiate preferentially into Treg cells rather than Th17 cells. To explain the above-mentioned contradiction, we used an experimental colitis model and found that LGG administration alleviated the DSS-induced colitis in mice, as indicated by decreases in weight loss and disease activity index. Moreover, SLC5A12 blockade (using a specific antibody) further reduced the colonic histological inflammatory score and decreased secretion of proinflammatory cytokines such as IFN-γ, IL-6, IL-17F, and IL-21. Notably, SLC5A12 blockade abolished the LGG-induced differentiation of the IL-17⁺CD4⁺ T (Th17) cells but significantly increased the frequency of Foxp3⁺CD4⁺ T (Treg) cells in the colonic lamina propria. Furthermore, a higher intracellular lactate concentration was observed in the colonic CD4⁺ T cells isolated from the LGG-treated colitic mice compared with other groups. Additionally, we also found elevated levels of oxidative stress indicators such as MDA and H₂O₂, as well as excessive reactive oxygen species (ROS) in colonic tissue of DSS-treated only mice, while LGG can scavenge ROS by inducing nuclear factor-erythroid 2-related factor 2 (Nrf2) expression in enterocytes. Conclusions: Altogether, these results indicate that LGG might alleviate preclinical colitis by modulating the Th17/Treg balance, and SLC5A12 blockade appears to enhance the anti-inflammatory properties of LGG. Full article

Background: Brain microvascular endothelial cells (BMECs) form the blood–brain barrier (BBB), a highly selective interface that restricts paracellular diffusion and regulates the transport of nutrients and drugs into the central nervous system via specialized transporters and receptors. Tight junction-associated protein 1 (Tjap1), also termed protein incorporated later into tight junctions (Pilt), has been localized to tight junctions (TJs) in epithelial cells and to the trans-Golgi network in fibroblasts; however, its expression, subcellular localization, and functional significance in BMECs are still unknown. Methods: We characterized Tjap1 subcellular localization in mouse and human BMEC cell lines as well as primary mouse BMECs by immunofluorescence with and without pharmacological Golgi disruption by treatment with Brefeldin A, Golgicide A or Pitstop 2. CRISPR/Cas9-mediated Tjap1 knockout cells were generated and examined with regard to their Golgi morphology using immunostaining. Tjap1 mRNA localization was examined by RNAscope in situ hybridization. Quantitative real-time PCR and Western blot was performed to assess the expression of BBB-associated efflux transporters, solute carrier transporters, and cellular receptors in control and Tjap1 knockout cells. Results: Tjap1 predominantly localized to the cis-Golgi compartment, co-localizing with Gm130 rather than Tgn38, and was absent from TJs in BMECs. Tjap1 knockout induced pronounced Golgi fragmentation BMECs. Importantly, Tjap1 knockout significantly downregulated mRNA-expression of Abcb1a, Abcb1b, Abcc4, Slc2a1, Slc7a1, Slc7a5 and Tfrc, while Abcg2 was upregulated. At the protein level, a decrease in the protein levels of Abcb1, Abcc4, Slc2a1, Slc7a1, and Tfrc was observed in Tjap1 knockout cEND cells. Conclusions: In BMECs, Tjap1 is a cis-Golgi-associated protein required for the structural integrity of the Golgi apparatus. Its deletion is associated with Golgi fragmentation and significant alterations in the mRNA and protein expression of drug transporters and receptors at the BBB. These findings identify Tjap1 as a candidate regulator of both Golgi architecture and the BBB transporter profile in vitro, with potential implications for modulating drug transport across the BBB. Full article

Smart shipping and achieving net-zero emissions have become pressing priorities in maritime transport, yet limited research has integrated sustainable shipping development with green finance decision-making. To address this gap, this study applies the AHP–RDEMATEL–TOPSIS approach to analyze the interrelationships and relative importance of key sustainability factors and to identify optimal green financing instruments. Incorporating ESG dimensions, the research conducted a survey of large international exporters in Taiwan and senior managers of shipping companies. The results reveal that green infrastructure is the most critical factor for container shipping lines, while energy efficiency and renewable energy technologies are dominant for bulk carriers and shippers. Corporate reputation and image emerge as primary factors impacted across all three groups. In financing decisions, green bonds are most suitable for container lines, whereas green equities are best suited for bulk carriers. This study bridges the theoretical gap between sustainability assessment and finance, providing practical guidance for shipping companies’ financial departments seeking to align decarbonization goals with effective green financing solutions. Ultimately, the primary contribution of this study lies in establishing an empirically validated, multi-criteria decision support framework that empowers maritime stakeholders to systematically optimize their green investment portfolios amid the global transition towards net-zero emissions. Full article

Cancer progression is closely linked to the enhanced uptake of extracellular amino acids, mediated by specific transporters that support biosynthesis, metabolic activity, and energy production through the tricarboxylic acid cycle. By increasing the expression of these transporters, tumor cells secure a continuous amino acid supply that sustains the proliferation, metabolic balance, and activation of major signaling pathways. While most studies have emphasized post-translational control of amino acid transporters, such as phosphorylation, ubiquitination, glycosylation, and palmitoylation, emerging evidence highlights regulatory crosstalk between these transporters and other membrane proteins, including G protein-coupled receptors and receptor tyrosine kinases. This review summarizes the current literature on the receptor-mediated mechanisms governing amino acid uptake and explores how interactions among families of membrane proteins contribute to the regulation of transporter activity. Full article

Ammonia, as a hydrogen carrier and clean fuel, has an increasingly urgent demand for large-scale transportation. Utilizing the existing refined oil pipeline network for sequential transportation of ammonia and refined oil is an economically and efficiently feasible solution. However, the unique micro-solubility characteristics of ammonia and refined oil can cause significant differences in the mixing mechanism of the two substances during sequential transportation in the pipeline compared to traditional oil products. This study conducts transient flow numerical simulation and mechanism research on the mixing problem during the sequential transportation process of ammonia and refined oil under the influence of micro-solubility transfer. Using the ANSYS Fluent platform and combining it with the dynamic mesh technology, a sequential transportation pipeline model was constructed. In the VOF multiphase flow model framework, the Fick diffusion and convective transfer theories were coupled. Through the development of user-defined functions, a transfer model was established to describe the ammonia dissolution process in refined oil during sequential transportation. This model characterizes the axial transfer process of the two-phase flow and the dissolution transfer in the pipeline. Then, the correctness and accuracy of the transfer model were verified, proving that the model has reliable simulation capabilities. To evaluate the comprehensive influence of various engineering factors on the mixing law, this study selected seven key parameters. It then designed and simulated multiple sets of comparative conditions. The influence of each parameter on the development of the mixing section was analyzed, and a sensitivity analysis was conducted. Subsequently, using the growth rate of the mixing length (dL/dt) as the dependent variable to represent the dynamic development of the mixing process, and using the above seven parameters as independent variables, a semi-empirical fitting formula was established. This formula can comprehensively reflect the coupling effect of multiple factors. The results show that the model has good generalization ability and extrapolation robustness. It provides a prediction model and theoretical tool with certain engineering practical value. This can be used for predicting the amount of mixing and optimizing operating parameters in actual pipeline sequential transportation systems. Full article

Electric vehicles are an important carrier for achieving energy savings and emission reductions in the transportation sector. As the decision-making core of the powertrain, the energy management strategy is responsible for power allocation and energy scheduling and directly determines vehicle economy, power-source lifetime, and overall performance. Model predictive control can handle multiple constraints and objectives within a prediction horizon and realize online closed-loop decision-making via receding-horizon optimization and has become an important research direction for energy management of electric vehicles. This paper presents the basic principles and typical modeling framework of model predictive control and reviews its research progress in hybrid electric vehicle energy management. The related studies are categorized and comparatively analyzed from three perspectives—prediction methods, solution strategies, and optimization objectives—and the characteristics of different approaches are summarized. The review shows that model predictive control has advantages in multi-objective trade-offs and adaptation to time-varying operating conditions. However, practical implementation still faces significant barriers, including prediction uncertainty and computational complexity. Finally, the challenges and future directions of model-predictive-control-based energy management strategies are discussed. Full article

Organic-type solar cells containing an active layer of block copolymer donor PTB7-Fx (x = 0, 20, and 100), based on benzo [1,2-b:4,5-b’]dithiophene and variably fluorinated thieno [3,4-b]thiophene units, and fullerene acceptor [6,6]phenyl-C₇₁-methylbutyrate, were constructed. The active layer thin film of the solar cells was obtained from a dichlorobenzene solution at an established concentration via spin-coating of the donor–acceptor mixture in the presence of solvent additives such as 3% diiodooctane and 1% triethyl phosphate. Organic photovoltaic elements with normal device architecture were prepared on glass substrates using an indium tin oxide anode, a spin-coated hole transporting layer of poly(ethylene dioxythiophene):polystyrenesulfonate, the aforementioned active layer, followed by an electron transporting layer of zinc oxide nanoparticles, and finally a magnetron sputtered silver (Ag) top-electrode. The optical properties, thin film morphology, and the thickness of the active layers were investigated. Additionally, current density–voltage characteristics and impedance spectra of photovoltaic devices were measured. It was found that PTB7-Fx:PC₇₁BM-based solar cells processed in the presence of two types of solvent additives, diiodooctane and triethyl phosphate, with a sputtered Ag top-electrode display similar absorption and quantum efficiency spectra, as well as comparable current density–voltage characteristics and efficiencies to the same devices fabricated without additives. The diiodooctane solvent additive preferably dissolves the fullerene component and has a positive effect on fill factor enhancement, impedance spectra improvement, and amelioration in charge carrier transport and collection, whereas the triethyl phosphate solvent additive preferentially dissolves the copolymer donor and has a more pronounced impact on the refined morphology of the thin film active layers. Full article