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LPS causes pericyte loss and microvascular dysfunction via disruption of Sirt3/angiopoietins/Tie-2 and HIF-2 alpha/Notch3 pathways

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成果类型:
期刊论文
作者:
Zeng, Heng;He, Xiaochen;Tuo, Qin-hui;Liao, Duan-fang;Zhang, Guo-qiang;...
通讯作者:
Chen, Jian-xiong
作者机构:
[Zeng, Heng; Chen, Jian-xiong; He, Xiaochen] Univ Mississippi, Med Ctr, Dept Pharmacol & Toxicol, Sch Med, Jackson, MS 39216 USA.
[Liao, Duan-fang; Tuo, Qin-hui] Hunan Univ Chinese Med, Sch Integrated Chinese & Western Med, Changsha 410208, Hunan, Peoples R China.
[Zhang, Guo-qiang] China Japan Friendship Hosp, Emergency Dept, Beijing 100029, Peoples R China.
通讯机构:
[Chen, Jian-xiong] U
Univ Mississippi, Med Ctr, Dept Pharmacol & Toxicol, Sch Med, Jackson, MS 39216 USA.
语种:
英文
期刊:
Scientific Reports
ISSN:
2045-2322
年:
2016
卷:
6
期:
1
页码:
20931
基金类别:
NIHUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USA [HL102042]; NATIONAL HEART, LUNG, AND BLOOD INSTITUTEUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Heart Lung & Blood Institute (NHLBI) [R01HL102042, R01HL102042, R01HL102042, R01HL102042, R01HL102042, R01HL102042, R01HL102042] Funding Source: NIH RePORTER
机构署名:
本校为其他机构
院系归属:
中西医结合学院
摘要:
Recent studies reveal a crucial role of pericyte loss in sepsis-associated microvascular dysfunction. Sirtuin 3 (SIRT3) mediates histone protein post-translational modification related to aging and ischemic disease. This study investigated the involvement of SIRT3 in LPS-induced pericyte loss and microvascular dysfunction. Mice were exposed to LPS, expression of Sirt3, HIF-2α, Notch3 and angiopoietins/Tie-2, pericyte/endothelial (EC) coverage and vascular permeability were assessed. Mice treated with LPS significantly reduced the expression of...

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