BIOCHEMICAL ENGINEERING JOURNAL
·
2022
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IF 4.446
Chenyang Qi,Yipin Zhang,Jing Tu
Nanomaterial-based antimicrobial strategies have emerged as powerful tools to combat microbial resistance, avoiding side effects of misusing antibiotics. In this work, the zinc oxide-based nanohybrid (designated as [email protected] ε-PL) as broad-spectrum antibacterial agents were fabricated in a facile two-step process. To be specific, ZnO was coated with near-infrared (NIR)-photoresponsive polydopamine (PDA), and then coupled with the antimicrobial peptide (AMP) (ε-poly- L -lysine, ε-PL). The as-prepared [email protected] ε-PL can effectively contact and capture bacteria, and then exhibit an excellent photothermal effect, i.e . , the temperature rises rapidly to 53.2 °C (100 μg/ml) under 808 nm NIR light irradiation for 10 min. The synergistic effect of ε-PL, ZnO and photothermal agent PDA contributes to the excellent antibacterial efficiency of [email protected] ε-PL (<100 μg/ml) with 808 nm irradiation, that is, 99.70% and 100.00% against Gram-negative bacteria ( Escherichia coli , E. coli ) and Gram-positive bacteria ( Staphyloccocus aureus , S. aureus ), respectively. Further experiments indicated the [email protected] ε-PL ultimately lead to bacterial death by disrupting cell integrity, leaking of intracellular components (e.g., nucleic acids). Moreover, [email protected] ε-PL can effectively remove 70.84% of S. aureus biofilms. Overall, NIR-responsive [email protected] ε-PL has great potential in the field of infection treatment.
研究领域:
纳米技术
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生物医学工程
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抗菌研究
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光热治疗
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产品关联
DOI
高影响因子
NUCLEIC ACIDS RESEARCH
·
2021
·Vol. 49
·期 21
·12306-12319
·
IF 16.971
Wang Huawei,Shan Xiajing,Ren Mengtian,Shang Mengdi,Zhou Chuanzheng
DNA damage and apoptosis lead to the release of free nucleosomes—the basic structural repeating units of chromatin—into the blood circulation system. We recently reported that free nucleosomes that enter the cytoplasm of mammalian cells trigger immune responses by activating cGMP-AMP synthase (cGAS). In the present study, we designed experiments to reveal the mechanism of nucleosome uptake by human cells. We showed that nucleosomes are first absorbed on the cell membrane through nonspecific electrostatic interactions between positively charged histone N-terminal tails and ligands on the cell surface, followed by internalization via clathrin- or caveolae-dependent endocytosis. After cellular internalization, endosomal escape occurs rapidly, and nucleosomes are released into the cytosol, maintaining structural integrity for an extended period. The efficient endocytosis of extracellular nucleosomes suggests that circulating nucleosomes may lead to cellular disorders as well as immunostimulation, and thus, the biological effects exerted by endocytic nucleosomes should be addressed in the future.
研究领域:
细胞生物学
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免疫学
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分子生物学
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产品关联
DOI
PubMed
高影响因子
International Journal of Greenhouse Gas Control
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2019
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IF 3.231
Fan Cao,Hongxia Gao,Qian Xiong,Zhiwu Liang
CO 2 absorption performance for various blended N ,N- dimethylethanolamine (DMEA) solutions in the presence of absorption promoters including Monoethanolamine (MEA), Piperazine (PZ), 2-(Ethylamino)ethanol (EAE), 2-(Methylamino)ethanol (MAE) and 2-Amino-2-methyl-1-propanol (AMP) was investigated in terms of CO 2 absorption flux by using a polytetrafluoroethylene (PTFE) hollow fiber membrane contactor. The experimental results show that the CO 2 absorption flux increases with a reasonable increase in liquid velocity, liquid temperature and total amine concentration. Also, the CO 2 absorption flux can increase by increasing gas velocity, CO 2 partial pressure but decrease with the increased lean CO 2 loading. In addition, it can be found that all of the investigated activated amines can improve the CO 2 absorption flux of aqueous DMEA solution. For fresh amine solution, the order of CO 2 absorption flux for the investigated amine blends can be ranked as: DMEA < DMEA + AMP < DMEA + MEA < DMEA + EAE < DMEA + MAE < DMEA + PZ. By contrast, for the amine solution with CO 2 loading of over 0.3 mol/mol, the order has also changed accordingly and can be ranked as: DMEA < DMEA + AMP < DMEA + EAE < DMEA + MAE < DMEA + MEA < DMEA + PZ. The DMEA + PZ mixture presents a significant improvement up to 52.44% in CO 2 absorption flux compared to that of single DMEA solution, and can be considered as a promising alternative for CO 2 capture.
研究领域:
化学工程
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环境科学
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膜技术
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产品关联
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2023
·
IF 8.6
Rui Zhang,Yufan Li,Xinwei He,Yingjie Niu,Chao'en Li,Mohammad Waleed Amer,Francesco Barzagli
Mixing amines with different properties is considered a smart strategy for developing efficient aqueous solutions for reversible CO 2 capture. Specifically, dual-amine blends containing the tertiary amine 2-dimethylamino-2-methyl-1-propanol (2DMA2M1P) have proven to be particularly advantageous due to significantly lower regeneration costs compared to conventional sorbents. With the aim of formulating high-efficiency sorbents, in this work we evaluated the improvement in the CO 2 capture performance of such dual-amine blends by adding a further amine to form trio-amine systems: the use of three amines with different characteristics could further emphasize the advantages obtainable during both absorption and desorption. We formulated three new different aqueous solutions prepared by mixing 2DMA2M1P with the reaction rate promoter ethanolamine (MEA) and the absorption capacity promoter 2-amino-2-methyl-1-propanol (AMP) in different molar ratios. For each blend, the CO 2 solubility at equilibrium, the CO 2 absorption rate from a gaseous mixture, the regeneration rate at T = 373 K and the energy requirement for desorption were determined experimentally. In addition, to better understand the capture mechanism, 13 C NMR spectroscopy was employed to evaluate the speciation of each blend during the CO 2 absorption. Their CO 2 capture performance was compared with that of the benchmark aqueous MEA and two 2DMA2M1P-based dual-amine mixtures, obtained with the same procedure. As a finding, all formulated trio-amine blends have superior CO 2 equilibrium solubility and desorption performance compared with MEA 5 M. Noteworthy, the comparison with similar dual-amine systems highlighted the role of a suitable third amine in order to obtain enhance both absorption and desorption efficiencies. Among the formulated systems, MEA-2DMA2M1P-AMP (1:2:2) is potentially the most suitable to replace MEA in CO 2 capture processes after a careful cost-benefit analysis on larger scale systems.
研究领域:
化学工程
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环境科学
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材料科学
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产品关联
DOI
高影响因子
TOXICOLOGY LETTERS
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2018
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IF 3.166
Yisen Cheng,Gaojian Chen,Li Wang,Jiamin Kong,Ji Pan,Yue Xi,Feihai Shen,Zhiying Huang
Triptolide is a major active ingredient of tripterygium glycosides, used for the therapy of immune and inflammatory diseases. However, its clinical applications are limited by severe male fertility toxicity associated with decreased sperm count, mobility and testicular injures. In this study, we determined that triptoide-induced mitochondrial dysfunction triggered reduction of lactate and dysregulation of fatty acid metabolism in mouse Sertoli cells. First, triptolide induced mitochondrial damage through the suppressing of proliferator-activated receptor coactivator-1 alpha (PGC-1α) activity and protein. Second, mitochondrial damage decreased lactate production and dysregulated fatty acid metabolism. Finally, mitochondrial dysfunction was initiated by the inhibition of sirtuin 1 (SIRT1) with the regulation of AMP-activated protein kinase (AMPK) in Sertoli cells after triptolide treatment. Meanwhile, triptolide induced mitochondrial fatty acid oxidation dysregulation by increasing AMPK phosphorylation. Taken together, we provide evidence that the mechanism of triptolide-induced testicular toxicity under mitochondrial injury may involve a metabolic change.
研究领域:
药理学
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毒理学
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生殖生物学
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细胞代谢
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产品关联
DOI
PubMed
高影响因子
Frontiers in Nutrition
·
2022
·
IF 6.59
Zhao Guangshan,Yang Lian,Zhong Wenshen,Hu Yuze,Tan Yu,Ren Zhe,Ban Qiuyan,Yang Chung S.,Wang Yifei,Wang Zhiping
Resveratrol (RES) is considered to be an activator of AMP-activated protein kinase (AMPK) with many reported health benefits. Polydatin (POD) is a natural precursor and glycosylated form of RES. The glycoside structure of POD alters the bioactivity. Overnutrition-stimulated reactive oxygen species (ROS) promote the AMPK suppression and metabolic dysregulation. The present work compared the effects of POD and RES in ameliorating energy homeostasis imbalance in mice fed a high-fructose diet and elucidated the underlying mechanisms of action. Our results showed that POD elevated the fecal levels of valeric acid and caproic acid via modification of gut microbiota, while RES did not significantly influence the levels of fecal short-chain fatty acids (SCFAs). Both POD and RES markedly decreased the oxidative stress and activated the AMPK signaling pathways in the liver. POD and RES exerted a similar effect in alleviating glucose dysmetabolism, but POD was more effective in ameliorating lipid dysmetabolism than RES. Furthermore, valeric acid and caproic acid alone can activate the AMPK and ameliorate hypercholesterolemia, and enhance the effects of POD on improving lipid metabolism in mice. Overall, for the first time, we demonstrated that POD administration elevated the fecal levels of valeric acid and caproic acid by modifying gut microbiota, thus promoting AMPK activation may be the underlying mechanism that POD is superior to RES in alleviating the lipid dysmetabolism. Our results suggest that POD may be an alternative for RES as an AMPK activator.
研究领域:
药理学
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营养学
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代谢性疾病
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胃肠病学
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分子生物学
✓ 已验证
DOI
PubMed
高影响因子
PHYTOMEDICINE
·
2023
·
IF 7.9
Chao Meng,Lingye Zhou,Lin Huang,Qi Gu,Xinyue Du,Cheng Wang,Fanglan Liu,Chunhua Xia
Background Hypercholesterolemia is widely implicated in the etiology of coronary heart disease , stroke, and dementia. Evidence suggests that chlorogenic acid (CA) reduces the risk of cardiovascular disease. Purpose The current study aims to explore the underlying molecular mechanism of CA in lowering cholesterol based on pregnane X receptor (PXR) and sterol regulatory element-binding protein 2 (SREBP2) regulatory pathways and their interactions with heat shock protein 90 (HSP90). Methods A hypercholesterolemic mouse model, HepG2 and Caco2 cell models, metabolomics analysis, and co-immunoprecipitation (COIP) were used to study the mechanism of CA lowering cholesterol. Results Treatment of the hypercholesterolemic mice with CA for 12 weeks significantly reduced body weight, blood lipid, hepatic lipid accumulation , and increased lipid excretion. The nuclear aggregation of PXR and SREBP2 was inhibited simultaneously. In addition, the expression of downstream target genes, including Niemann-pick C1-like 1 (NPC1L1) and 3‑hydroxy-3-methylglutaryl-CoA reductase (HMGCR), was downregulated after CA administration. Furthermore, in HepG2 and Caco2 cell models, CA reduced intracellular cholesterol levels by inhibiting the nuclear translocation of PXR and SREBP2 and the expression of NPC1L1 and HMGCR. SREBP2 interacts with PXR through HSP90, and CA reduces the binding stability of SREBP2 and HSP90 and enhances the binding of PXR and HSP90, thus reducing the nuclear accumulation of SREBP2 and PXR simultaneously. Moreover, CA promoted the phosphorylation of AMP-activated protein kinase (AMPK) and its binding to SREBP2. This was not conducive to the binding of HSP90 and SREBP2 but enhanced the binding of HSP90 and PXR, thereby inhibiting the nuclear translocation of SREBP2 and PXR and reducing intracellular cholesterol levels. However, no noticeable direct binding between AMPK and PXR was observed. Conclusion CA downregulates NPC1L1 and HMGCR expression by acting on the AMPK/SREBP2 direct pathway and the AMPK/SREBP2/HSP90/PXR indirect pathway, thus retaining cholesterol homeostasis.
研究领域:
药理学
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分子生物学
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心血管疾病
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代谢组学
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产品关联
DOI
PubMed
高影响因子
Journal of Functional Foods
·
2019
·
IF 3.197
Zhenlong Chen,Yuhui Yang,Shumei Mi,Qingsheng Fan,Xiaoming Sun,Baichuan Deng,Guoyao Wu,Yafei Li,Quancheng Zhou,Zheng Ruan
Chlorogenic acid (CGA) is a type of phenolic acid that has antioxidant and anti-inflammatory activities. In this study, we investigated the hepatoprotective effect of CGA in lipopolysaccharide (LPS)-treated rats. Supplementation with CGA attenuated ( P < 0.05) hepatocyte necrosis and inflammatory cell infiltration, decreased ( P < 0.05) the activities of serum transaminases and alkaline phosphatase and the level of total bilirubin, and increased ( P < 0.05) the level of serum total protein in comparison with the LPS-only group. In addition, CGA potently inhibited ( P < 0.05) the LPS-induced drop in the activities of mitochondrial NADH dehydrogenase and ATP synthase and the contents of ATP and AMP in the liver. Furthermore, CGA could partially counteract the changes induced by lipopolysaccharide in many metabolic pathways, such as energy metabolism, amino acid metabolism, and glutathione metabolism. In summary, our study showed that CGA supplementation had a protective effect against LPS-induced chronic liver injury.
研究领域:
药理学
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肝病学
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免疫学
·
代谢学
✓ 已验证
DOI
高影响因子
CHEMICO-BIOLOGICAL INTERACTIONS
·
2022
·
IF 5.168
Xueyun Liu,Man Hu,Chen Ye,Lihong Liao,Chang Ding,Lijuan Sun,Jichao Liang,Yong Chen
It is well known that the excessive accumulation of lipid in hepatocytes is one of the important causes of non-alcoholic fatty liver disease (NAFLD). The purpose of this study was to explore the effects of isosilybin on lipid metabolism in free fatty acids (FFAs) or TO901317-induced HepG2 cells. Cells were treated with FFAs (oleic acid: palmitic acid , 2:1) or TO901317 to induce steatosis in vitro. Intracellular triglyceride (TG) content was quantified using commercial assay kits. The mRNA and protein expression of genes involved in fatty acid uptake, synthesis and oxidation were analyzed by RT-qPCR and western blotting . Selected biological pathways regulated by isosilybin treatment were determined by GO and KEGG analysis. The results showed that isosilybin significantly reduced TG levels in FFAs- and TO901317-induced HepG2 cells. Further studies showed that isosilybin treatment decreased the mRNA and protein expression of lipid synthesis genes Srebp-1c, Pnpla3, Acc and Fas , as well as the mRNA expression of fatty acid uptake gene CD36, whereas increased the mRNA levels of lipid oxidation genes Pparα, Acox1 and Cpt1α, as well as the mRNA expression of lipid export gene Mttp, in FFAs-induced HepG2 cells. Moreover, TO901317 was employed to induce endogenous lipid synthesis and steatosis, and the expression of Srebp-1c and its target genes in TO901317-induced hepatocytes was basically similar to that in FFAs-induced hepatocytes following isosilybin treatment. We also observed the increased level of phosphorylated AMP kinase (AMPK) after isosilybin treatment, while this effect was reversed after further treatment with AMPK inhibitor , compound C. The results of GO and KEGG analysis indicated that the pathways of fatty acid and TG metabolism were regulated by isosilybin. Interestingly, we found that treatment with the diastereoisomer A of isosilybin increased TG level, while exposure to the diastereoisomer B of isosilybin decreased TG level in FFAs-induced HepG2 cells. The above results suggest that isosilybin can inhibit lipid synthesis and activate lipid oxidation through AMPK signaling pathway, thereby improving steatosis of hepatocytes, and isosilybin B is the basis of its active substance.
研究领域:
分子生物学
·
细胞生物学
·
药理学
·
代谢紊乱
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Biomaterials Science
·
2023
·
IF 6.6
HaiYang Wang,Minzhao Lin,Gengjia Chen,Zecong Xiao,Xintao Shuai
The treatment of drug-resistant tumors poses a significant challenge in the field of tumor therapy. Disrupting the homeostasis of reactive oxygen species (ROS) within tumor cells may represent a pivotal strategy for overcoming the prevalent issue of drug resistance. However, the restricted sustainability of ROS generation and the increased autophagy capacity exhibited by tumor cells hinder the application of ROS-based therapies. In this study, we developed liposome nanoparticles (Ato/CQ@L) for co-encapsulation of atorvastatin (Ato), an activator of AMP-activated protein kinase (AMPK), and chloroquine (CQ), an autophagy inhibitor. Upon internalization by tumor cells, Ato upregulated carnitine palmitoyltransferase 1(CPT1) concentration and promoted fatty acid oxidation (FAO) within the tumor cells. The process of FAO coupled with an abundance of fatty acid substrates, facilitates a sustained generation of ROS production. Concurrently, a positive feedback loop is established between escalated concentration of ROS and AMPK protein levels, resulting in a persistent elevation in ROS levels. In addition, CQ disrupted lysosomes, leading to an increased lysosomal pH and reducing autophagy in tumor cells. In both in vivo and in vitro experiments, the Ato/CQ@L treatment group exhibited a considerable enhancement in tumor cell apoptosis, validating the efficacy of this combined therapy. In summary, the combined therapy involving Ato and CQ addresses the inherent limitations of conventional ROS therapy, which include insufficient ROS production and increased autophagy. This approach holds significant potential as a treatment strategy for drug-resistant triple-negative breast cancer.
研究领域:
肿瘤学
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药理学
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纳米技术
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分子生物学
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细胞生物学
✓ 已验证
DOI
PubMed
高影响因子
ACS Applied Materials & Interfaces
·
2021
·
IF 9.229
Yunsu Ma,Huanghuang Xu,Bo Sun,Silin Du,Shuai Cui,Li Zhang,Ning Ding,Dongzhi Yang
The combination of photodynamic therapy (PDT) and chemodynamic therapy (CDT) has been continuously explored in the antibacterial aspect and has achieved more effective antibacterial effect than a single therapy. We design a pH-responsive O2 and H2O2 self-supplying zeolitic imidazolate framework-67 (ZIF-67) nanosystem for PDT/CDT of wound infection. Under the acidic inflammatory conditions, ZIF-67 can degrade to produce Co2+ and release CaO2 and graphene quantum dots (GQDs). The exposed CaO2 reacted with water to generate H2O2 and O2. The self-supplied O2 alleviates hypoxia at the site of inflammation and enhances external light-initiated GQD-mediated PDT, while H2O2 was catalyzed by endogenous Co2+ to produce hydroxyl radicals for Co2+-triggered CDT. In vitro and in vivo experiments confirm that CaO2/GQDs@ZIF-67 has a combined PDT/CDT effect. The antibacterial mechanism indicates that bacteria post-treated with CaO2/GQDs@ZIF-67 may be sterilized by reactive oxygen species-mediated oxidative stress and the leakage of bacterial contents. The experiments also find that CaO2/GQDs@ZIF-67 may activate the immune response and enhance the therapeutic effect by activating the cyclic GMP–AMP synthase–stimulator of interferon genes signaling pathway.
研究领域:
纳米技术
·
生物医学工程
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药学
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传染病
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材料科学
✓ 已验证
DOI
PubMed
高影响因子
SCIENCE OF THE TOTAL ENVIRONMENT
·
2021
·
IF 7.963
Yi Fan,Guangrong Sun,Han Yeong Kaw,Lizhong Zhu,Wei Wang
Nucleotides, as the basic building blocks of nucleic acids , widely exist in aqueous environment. In this study, we developed a solid phase extraction-high performance liquid chromatography-tandem mass spectrometry (SPE-UPLC-MS/MS) method for the analysis of 5′-adenosine monophosphate (AMP), 5′-uridine monophosphate (UMP), 5′-cytidine monophosphate (CMP) and 5′-guanosine monophosphate (GMP). The method achieved limits of detection (LODs) of 0.1–1.0 ng/L, and recoveries of 85–95% for the four tested nucleotides. The occurrence and concentrations of the four nucleotides in water from eight representative drinking water treatment and distribution systems in China were determined using this method. All four nucleotides were detectable in water treatment plant (WTP) influent and effluent, at concentrations of up to 30 ng/L and with occurrence frequency of around 90%. The concentrations of identified nucleotides increased 3–10 times after 10 km of water age in the water distribution system . Biological filters and coagulation increased the concentrations of nucleotides, conversely, active carbon, ozonation , and ultrafiltration membrane removed nucleotides in water. The effects of active carbon and coagulation were further confirmed using laboratory-controlled experiment. In addition, monochlorinated nucleotides were identified as the chlorination products of nucleotides.
研究领域:
环境科学
·
水处理
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分析化学
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色谱学
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质谱学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）