移植
肾缺血
肾
下调和上调
小RNA
再灌注损伤
肾移植
癌症研究
药理学
医学
缺血
化学
细胞生物学
生物
内科学
生物化学
基因
作者
Lang Shi,Hongchu Zha,Hua Huang,Yao Xia,Huimin Li,Jing Wang,Ruchi Yue,Chenglong Li,Jiefu Zhu,Zhixia Song
出处
期刊:American Journal of Physiology-renal Physiology
[American Physiological Society]
日期:2024-09-12
卷期号:327 (5): F910-F929
标识
DOI:10.1152/ajprenal.00409.2023
摘要
This study identifies miR-199a-5p as a key regulator in renal ischemia-reperfusion injury through microRNA sequencing in mouse models and human delayed graft function. miR-199a-5p worsens renal IRI by aggravating graft dysfunction, tubular injury, and immune response, while its inhibition shows protective effects. miR-199a-5p downregulates A-kinase anchoring protein 1 (AKAP1), reducing dynamin-related protein 1 (Drp1)-s637 phosphorylation, increasing mitochondrial fission, and causing dysfunction. Targeting the miR-199a-5p/AKAP1/Drp1 axis offers therapeutic potential for renal IRI, as AKAP1 overexpression preserves mitochondrial integrity by maintaining Drp1-s637 phosphorylation.
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