粒体自噬
帕金
品脱1
肾缺血
肾
线粒体
缺血
自噬
再灌注损伤
细胞凋亡
药理学
医学
细胞生物学
化学
内分泌学
生物
内科学
生物化学
疾病
帕金森病
作者
Fan Zhao,Jiefu Zhu,Mingjiao Zhang,Yanwen Luo,Yuzhen Li,Lang Shi,Jiao Huang,Halinuer Shadekejiang,Shengyu Dong,Xiongfei Wu
摘要
Abstract Renal ischemia–reperfusion injury (IRI) is mainly responsible for acute kidney injury for which there is no effective therapy. Accumulating evidence has indicated the important role of mitophagy in mitochondrial homeostasis under stress. OGG1 (8‐oxoguanine DNA glycosylase) is known for functions in excision repair of nuclear and mitochondrial DNA. However, the role of OGG1 in renal IRI remains unclear. Herein, we identified OGG1, induced during IRI, as a key factor mediating hypoxia‐reoxygenation‐induced apoptosis in vitro and renal tissue damage in a renal IRI model. We demonstrated that OGG1 expression during IRI negatively regulates mitophagy by suppressing the PINK1/Parkin pathway, thereby aggravating renal ischemic injury. OGG1 knockout and pharmacological inhibition attenuated renal IRI, in part by activating mitophagy. Our results elucidated the damaging role of OGG1 activation in renal IRI, which is associated with the regulatory role of the PINK1/Parkin pathway in mitophagy.
科研通智能强力驱动
Strongly Powered by AbleSci AI