Beclin 1 deficiency causes hepatic cell apoptosis via endoplasmic reticulum stress in zebrafish larvae

被引:13
|
作者
Dong, Guoping [1 ]
Zhang, Zhe [1 ]
Duan, Kun [1 ]
Shi, Wenpeng [1 ]
Huang, Rui [1 ]
Wang, Bangjun [1 ]
Luo, Lingfei [1 ]
Zhang, Yaoguang [1 ]
Ruan, Hua [1 ]
Huang, Honghui [1 ]
机构
[1] Southwest Univ, Sch Life Sci, Key Lab Freshwater Fish Reprod & Dev,Minist Educ, State Key Lab Breeding Base Ecoenvironm & Bioreso, 2 Tiansheng Rd, Chongqing 400715, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
autophagy; Beclin; 1; cell apoptosis; ER stress; protein aggregates; zebrafish; ER STRESS; AUTOPHAGY; GENE; ACTIVATION; EXPRESSION; PATHWAYS; PROTEINS; DISEASE; TARGET; YEAST;
D O I
10.1002/1873-3468.13712
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Beclin 1/Atg6 is an essential autophagy gene, and deficiency of this gene in organisms leads to impaired autophagic flux, usually with cell apoptosis; however, the causative mechanism of cell apoptosis is not clear. Here, we knocked out the beclin 1 gene in zebrafish and found that autophagic flux is disrupted in mutants. Beclin 1-deficient zebrafish live through embryogenesis but die at larval stage. We found accumulated protein aggregates and vigorous apoptosis in mutant larvae, predominantly in the liver. The hepatic cell apoptosis in mutants results from an endoplasmic reticulum (ER) stress response; however, it is not the leading cause of mutant larval lethality. Our work proposes that ER stress induces cell apoptosis in Beclin 1-deficient organisms.
引用
收藏
页码:1155 / 1165
页数:11
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