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SIRT1是2,3,5,4'-四羟基二苯乙烯-2-O-β-D-葡萄糖苷减轻人脐静脉内皮细胞衰老的靶基因。

SIRT1 Is the Target Gene for 2,3,5,4'-Tetrahydroxystilbene-2-O-β-D-Glucoside Alleviating the HUVEC Senescence.

作者信息

Guo Yan, Fan Wenxue, Xie Yuefeng, Cao Shuyu, Wan Haitong, Jin Bo

机构信息

College of Life Science, Zhejiang Chinese Medical University, Hangzhou, China.

College of Basic Medicine and Public Health, Zhejiang Chinese Medical University, Hangzhou, China.

出版信息

Front Pharmacol. 2020 Sep 8;11:542902. doi: 10.3389/fphar.2020.542902. eCollection 2020.

DOI:10.3389/fphar.2020.542902
PMID:33013385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7508177/
Abstract

This study aimed to explore the effects of 2,3,5,4'-tetrahydroxy-stilbene-2-O-β-d-glucoside (TSG) on the senescence of human umbilical vein cells (HUVEC) induced by hydrogen peroxide (HO) and to identify the potential targets mediating its protective action. HUVEC cells pre-treated with TSG for 24 h were exposed to HO treatment. TSG significantly decreased HO-induced cellular senescence, as indicated by reduced senescence-associated β-galactosidase (SA-β-gal) positive staining, the proportion of cells in the G1 phase, cell apoptosis, p21, and plasminogen activator inhibitor-1 (PAI-1) expression. Moreover, TSG promoted Sirtuin 1 (SIRT1) expression. When SIRT1 was inhibited by EX527 or SIRT1 siRNA, the effect of TSG is diminished according to the increased proportion of cells in the G1 phase, cell apoptosis, p21, and PAI-1 expression. Overall, our study established TSG as an anti-senescence compound that exerts its protective action by regulating SIRT1 expression.

摘要

本研究旨在探讨2,3,5,4'-四羟基二苯乙烯-2-O-β-D-葡萄糖苷(TSG)对过氧化氢(HO)诱导的人脐静脉细胞(HUVEC)衰老的影响,并确定介导其保护作用的潜在靶点。用TSG预处理24小时的HUVEC细胞接受HO处理。TSG显著降低了HO诱导的细胞衰老,表现为衰老相关β-半乳糖苷酶(SA-β-gal)阳性染色减少、G1期细胞比例降低、细胞凋亡减少、p21和纤溶酶原激活物抑制剂1(PAI-1)表达降低。此外,TSG促进了沉默调节蛋白1(SIRT1)的表达。当用EX527或SIRT1 siRNA抑制SIRT1时,根据G1期细胞比例增加、细胞凋亡增加、p21和PAI-1表达增加,TSG的作用减弱。总体而言,我们的研究确定TSG为一种抗衰老化合物,其通过调节SIRT1表达发挥保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/7508177/87ead6f8f504/fphar-11-542902-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/7508177/c03c3feddf0b/fphar-11-542902-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/7508177/35d57257bd1b/fphar-11-542902-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/7508177/86fc64ef976e/fphar-11-542902-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/7508177/60c97354afa3/fphar-11-542902-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/7508177/f01311c8b81a/fphar-11-542902-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/7508177/87ead6f8f504/fphar-11-542902-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/7508177/c03c3feddf0b/fphar-11-542902-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/7508177/35d57257bd1b/fphar-11-542902-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/7508177/86fc64ef976e/fphar-11-542902-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/7508177/60c97354afa3/fphar-11-542902-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/7508177/f01311c8b81a/fphar-11-542902-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf11/7508177/87ead6f8f504/fphar-11-542902-g006.jpg

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