细胞自噬分子机制的进展

被引:94
作者
冯文之 [1 ,2 ]
陈扬 [2 ]
俞立 [2 ]
机构
[1] 北京大学生命科学学院
[2] 清华大学-北京大学生命科学联合中心清华大学生命科学学院生物膜与膜生物工程国家重点实验室
关键词
细胞自噬; 自噬体; 溶酶体; Atg蛋白; 蛋白质降解;
D O I
10.13376/j.cbls/20150118
中图分类号
Q255 [细胞的衰老与死亡];
学科分类号
071003 [生理学];
摘要
细胞自噬是一类依赖于溶酶体的蛋白质降解途径,在真核生物中非常保守。自噬能够感受细胞所处环境的各种信号,如氨基酸、糖等营养物质的缺乏、p H值或渗透压的改变等,使细胞做出应激反应,在恶劣环境下存活。同时,自噬过程会清除细胞内错误折叠或聚集的蛋白质,受损或老化细胞器以维持细胞内部稳态。自噬发生时,细胞内部的胞质组分被包裹在自噬体中,自噬体与溶酶体融合进行降解,产生新的小分子,如氨基酸等供细胞重新利用。一系列研究发现自噬的信号通路非常复杂,已报道有40个自噬相关蛋白(Atg蛋白)参与了自噬体的形成过程。Atg蛋白按照一定步骤发挥功能,同时相互影响,利用内膜系统构建成一个闭合的双层膜结构。将对细胞自噬研究的历史、自噬分子机制的前沿进展进行综述。
引用
收藏
页码:859 / 866
页数:8
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