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基于细胞自噬探讨缺氧条件下黄芪多糖促进血管新生的机制 被引量:1
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作者 周严东 高娜 +6 位作者 陈叶飞 孙英新 张瑞峰 郑宇佳 李雅文 杨琳 姜希娟 《阿尔茨海默病及相关病杂志》 2023年第1期35-42,共8页
目的:探究黄芪多糖(astragalus polysaccharide,APS)在缺氧条件下促进血管新生的作用机制与靶点。方法:于体外鼠尾胶基质上种植胸主动脉血管段构建新生血管三维培养模型,随机分为对照组、APS25 mg·L^(-1)组,利用倒置显微镜观察新... 目的:探究黄芪多糖(astragalus polysaccharide,APS)在缺氧条件下促进血管新生的作用机制与靶点。方法:于体外鼠尾胶基质上种植胸主动脉血管段构建新生血管三维培养模型,随机分为对照组、APS25 mg·L^(-1)组,利用倒置显微镜观察新生血管生长情况。体外培养大鼠脑微血管内皮细胞,以氯化钴400μmol·L^(-1)诱导24 h,形成可复制的缺氧模型,随机分为7组(n=6):对照组、缺氧模型组、APS25 mg·L^(-1)组、自噬激动剂雷帕霉素10 mg·L^(-1)组,阳性对照药巴弗洛霉素组20mg·L-1,APS加雷帕霉素组,APS加巴弗洛霉素组。然后利用CCK-8比色法检测各组细胞的增殖活性;蛋白印迹法检测各组细胞自噬相关蛋白Becline-1、LC3B、P62的表达。结果:(1)血管新生实验:与对照组相比,经APS干预新生血管数量明显增多(P<0.05)。(2)细胞实验:与模型组相比,经APS治疗内皮细胞增殖能力提高(P<0.05),Becline-1、LC3B蛋白表达量下调(P<0.01)。结论:在缺氧条件下,黄芪多糖可通过促进血管内皮细胞增殖,促进血管新生,其机制可能与下调内皮细胞Becline-1、LC3B的表达以抑制自噬发生有关。 展开更多
关键词 血管新生 脑微血管内皮细胞 细胞自噬 细胞迁移 黄芪多糖 缺血性脑卒中
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Ginsenoside Rg1 protects against ischemia-induced neuron damage by regulating the rno-miRNA-27a-3p/PPARγaxis
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作者 YUE GUAN TINGTING ZHANG +6 位作者 JIANAN YU JIAWEI LIU WENYUAN LI yujia zheng JIALE WANG YUE LIU FENGGUO ZHAI 《BIOCELL》 SCIE 2023年第7期1583-1594,共12页
A preliminary miRNA screening showed that expression levels of rno-miRNA-27a-3p were significantly increased in the serum and brain tissues of rats undergoing cerebral ischemia.In recent years,there is evidence of the... A preliminary miRNA screening showed that expression levels of rno-miRNA-27a-3p were significantly increased in the serum and brain tissues of rats undergoing cerebral ischemia.In recent years,there is evidence of the protective capacity of the saponins extracted from panax ginseng and its primary active ingredient ginsenosideRg1oncerebral ischemic injury.Methods:Fetal rat neurons(FRNs)were cultured in glucose-and-serumfree medium and exposed to hypoxia to establish a cerebral ischemia model in vitro(oxygen and glucose deprivation model,OGD).Antioxidant indexes(CAT,SOD),inflammatory markers(MPO,TNF-αand IL-6),and the expression of apoptosis and proliferation associated proteins(NF kB-p65,Caspase 3-cleaved,BCL-2)were examined.Results:Pre-treatment of Rg1(30–100μg/mL)could effectively inhibit the decline of antioxidant indexes(CAT,SOD)and increase in inflammatory markers(MPO,TNF-αand IL-6),and effectively inhibited the apoptosis in FRNs induced by OGD in a gradient-dependent manner.The mechanism analysis showed that the role of Rg1 in protecting against ischemia-induced neuron damage depends on its indirect up-regulation of PPAR protein via suppression of rnomiRNA-27a-3p.Moreover,these effects of Rg1 could be reversed by exogenous rno-miRNA-27a-3p and PPAR gene silencing in FRNs exposed to OGD.Conclusion:To summarize,our study demonstrates that Rg1 could effectively attenuate neuronal damage caused by cerebral ischemia via the rno-miRNA-27a-3p/PPARγpathway.Further,clarification of the novel mechanism will certainly improve our previous understanding of the role of Rg1 and enhancing its level in treatments for alleviating ischemic brain injury. 展开更多
关键词 Ginsenoside Rg1 rno-miRNA-27a-3p PPARΓ Cerebral ischemia NEURON OGD
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TGF-βsignaling in health,disease,and therapeutics 被引量:2
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作者 Ziqin Deng Tao Fan +4 位作者 Chu Xiao He Tian yujia zheng Chunxiang Li Jie He 《Signal Transduction and Targeted Therapy》 SCIE CSCD 2024年第4期1466-1505,共40页
ransforming growth factor(TGF)-βis a multifunctional cytokine expressed by almost every tissue and cell type.The signal transduction of TGF-βcan stimulate diverse cellular responses and is particularly critical to e... ransforming growth factor(TGF)-βis a multifunctional cytokine expressed by almost every tissue and cell type.The signal transduction of TGF-βcan stimulate diverse cellular responses and is particularly critical to embryonic development,wound healing,tissue homeostasis,and immune homeostasis in health.The dysfunction of TGF-βcan play key roles in many diseases,and numerous targeted therapies have been developed to rectify its pathogenic activity.In the past decades,a large number of studies on TGF-βsignaling have been carried out,covering a broad spectrum of topics in health,disease,and therapeutics.Thus,a comprehensive overview of TGF-βsignaling is required for a general picture of the studies in this field.In this review,we retrace the research history of TGF-βand introduce the molecular mechanisms regarding its biosynthesis,activation,and signal transduction.We also provide deep insights into the functions of TGF-βsignaling in physiological conditions as well as in pathological processes.TGF-β-targeting therapies which have brought fresh hope to the treatment of relevant diseases are highlighted.Through the summary of previous knowledge and recent updates,this review aims to provide a systematic understanding of TGF-βsignaling and to attract more attention and interest to this research area. 展开更多
关键词 HOMEOSTASIS HEALING WOUND
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