粒体自噬
帕金
品脱1
细胞生物学
线粒体
内质网
脂肪组织
褐色脂肪组织
生物
白色脂肪组织
泛素
褐变
化学
生物化学
自噬
内科学
细胞凋亡
基因
帕金森病
医学
疾病
作者
Xuetao Ji,Xu Zhang,Tong Zhang,Xue Yao,Mengping He,C. Li,Yun Huang,Haoyu Wang,Jing Ju,Lie Cai,Yuzhu Wang,Ning Wang,Lijuan Fan,Hui Tong,Heng Fan,Qinsheng Chen,Qinwei Lu,Cong Li,Huiru Tang,Yongsheng Chang
标识
DOI:10.1038/s41467-025-61904-w
摘要
Abstract PINK1/Parkin-mediated ubiquitin-dependent mitophagy is a critical negative regulatory machinery for browning in the inguinal white adipose tissue (iWAT). However, the precise regulatory mechanism underlying PINK1/Parkin-mediated mitophagy during browning of iWAT remains largely unknown. Here we report that PNPLA7, an Endoplasmic Reticulum and mitochondria-associated membrane (MAM) protein, inhibits browning of iWAT by promoting PINK1/Parkin-mediated mitophagy upon cold challenge or β3-adrenergic receptor agonist treatment. With genetic manipulation in mice, we show that adipose tissue overexpressing PNPLA7 induces mitophagy, abolishes iWAT browning and interrupts adaptive thermogenesis. Conversely, conditional ablation of PNPLA7 in adipose tissue promotes browning of iWAT, resulting in enhanced adaptive thermogenesis. Mechanistically, PNPLA7 interacts with Parkin to promote mitochondrial recruitment of Parkin for mitophagy activation and mitochondria degradation by disrupting PKA-induced phosphorylation of Parkin under cold challenge. Taken together, our findings suggest that PNPLA7 is a critical regulator of mitophagy that resists cold-induced browning of iWAT, thus providing a direct mechanistic link between mitophagy and browning of iWAT.
科研通智能强力驱动
Strongly Powered by AbleSci AI