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CHOP通过下调自噬在内质网应激时加重肝细胞凋亡。

CHOP aggravates hepatocyte apoptosis upon endoplasmic reticulum stress by downregulating autophagy.

作者信息

Wu Jia-Yu, Han Bing, Yang Ting, Zheng Lu, Guo Yi-Xin, Li Jia-Yao, Guo Xiao-Yu, Yin Huan-Huan, Xie Ru-Jia

机构信息

Department of Pathophysiology, College of Basic Medical Sciences, Guizhou Medical University, Guiyang, Guizhou Province, China; Guizhou Provincial Key Laboratory of Pathogenesis and Drug Research on Common Chronic Diseases, College of Basic Medical Sciences, Guizhou Medical University, Guiyang, Guizhou Province, China.

Department of Pathophysiology, College of Basic Medical Sciences, Guizhou Medical University, Guiyang, Guizhou Province, China; Guizhou Provincial Key Laboratory of Pathogenesis and Drug Research on Common Chronic Diseases, College of Basic Medical Sciences, Guizhou Medical University, Guiyang, Guizhou Province, China.

出版信息

Cell Stress Chaperones. 2025 May;30(3):109-118. doi: 10.1016/j.cstres.2025.02.005. Epub 2025 Feb 27.

Abstract

Endoplasmic reticulum (ER) stress-induced apoptosis plays a crucial role in various liver diseases. Hepatocytes respond to ER stress by activating the unfolded protein response and autophagy, which is essential for maintaining ER homeostasis. However, failure to restore ER balance via autophagy contributes to apoptosis. In this study, we aimed to explore the role of C/EBP homologous protein (CHOP) in regulating ER stress-induced apoptosis in rat hepatocytes. We found that CHOP downregulates autophagy, aggravating apoptosis. Our results revealed that inhibition of CHOP expression enhanced autophagy and reduced DTT-induced apoptosis in BRL-3A cells, whereas CHOP overexpression worsened apoptosis. Chromatin immunoprecipitation assays revealed that CHOP negatively regulates autophagy-related genes, such as ATG12, ATG5, and LC3. These findings suggest that CHOP modulation plays a crucial role in ER stress-induced hepatocyte apoptosis by regulating autophagy.

摘要

内质网(ER)应激诱导的细胞凋亡在各种肝脏疾病中起关键作用。肝细胞通过激活未折叠蛋白反应和自噬来应对内质网应激,这对于维持内质网稳态至关重要。然而,未能通过自噬恢复内质网平衡会导致细胞凋亡。在本研究中,我们旨在探讨C/EBP同源蛋白(CHOP)在调节大鼠肝细胞内质网应激诱导的细胞凋亡中的作用。我们发现CHOP下调自噬,加重细胞凋亡。我们的结果表明,抑制CHOP表达可增强自噬并减少二硫苏糖醇(DTT)诱导的BRL-3A细胞凋亡,而CHOP过表达则使细胞凋亡恶化。染色质免疫沉淀分析表明,CHOP负向调节自噬相关基因,如ATG12、ATG5和LC3。这些发现表明,CHOP调节通过调控自噬在内质网应激诱导的肝细胞凋亡中起关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/936a/11968278/ceaaab4ad48b/gr1.jpg

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