旁分泌信号
粒体自噬
细胞生物学
胰岛素样生长因子结合蛋白
生长因子
炎症
生物
胰岛素样生长因子
医学
化学
免疫学
细胞凋亡
受体
内科学
生物化学
自噬
作者
Bangchuan Hu,Jingwen Zhu,Guohua Wu,Juan-Juan Cai,Xue Yang,Ziqiang Shao,Yang Zheng,Jun-Mei Lai,Ye Shen,Xianghong Yang,Jingquan Liu,Renhua Sun,Haiping Zhu,Xiangming Ye,Shi-Jing Mo
出处
期刊:Life Sciences
[Elsevier]
日期:2023-04-01
卷期号:322: 121653-121653
被引量:7
标识
DOI:10.1016/j.lfs.2023.121653
摘要
Inflammation-coupling tubular damage (ICTD) contributes to pathogenesis of septic acute kidney injury (AKI), in which insulin-like growth factor-binding protein 7 (IGFBP-7) serves as a biomarker for risk stratification. The current study aims to discern how IGFBP-7 signalling influences ICTD, the mechanisms that underlie this process and whether blockade of the IGFBP-7-dependent ICTD might have therapeutic value for septic AKI.In vivo characterization was carried out in B6/JGpt-Igfbp7em1Cd1165/Gpt mice subjected to cecal ligation and puncture (CLP). Transmission electron microscopy, immunofluorescence, flow cytometry, immunoblotting, ELISA, RT-qPCR and dual-luciferase reporter assays were used to determine mitochondrial functions, cell apoptosis, cytokine secretion and gene transcription.ICTD augments the transcriptional activity and protein secretion of tubular IGFBP-7, which enables an auto- and paracrine signalling via deactivation of IGF-1 receptor (IGF-1R). Genetic knockout (KO) of IGFBP-7 provides renal protection, improves survival and resolves inflammation in murine models of cecal ligation and puncture (CLP), while administering recombinant IGFBP-7 aggravates ICTD and inflammatory invasion. IGFBP-7 perpetuates ICTD in a NIX/BNIP3-indispensable fashion through dampening mitophagy that restricts redox robustness and preserves mitochondrial clearance programs. Adeno-associated viral vector 9 (AAV9)-NIX short hairpin RNA (shRNA) delivery ameliorates the anti-septic AKI phenotypes of IGFBP-7 KO. Activation of BNIP3-mediated mitophagy by mitochonic acid-5 (MA-5) effectively attenuates the IGFBP-7-dependent ICTD and septic AKI in CLP mice.Our findings identify IGFBP-7 is an auto- and paracrine manipulator of NIX-mediated mitophagy for ICTD escalation and propose that targeting the IGFBP-7-dependent ICTD represents a novel therapeutic strategy against septic AKI.
科研通智能强力驱动
Strongly Powered by AbleSci AI