Noncentrosomal microtubules regulate autophagosome transport through CAMSAP2-EB1 cross-talk

被引:8
|
作者
Wei, Jieli [1 ,2 ]
Xu, Honglin [1 ]
Meng, Wenxiang [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Genet & Dev Biol, State Key Lab Mol Dev Biol, Beijing, Peoples R China
[2] Univ Chinese Acad Sci, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
autophagy; CAMSAP2; EB1; noncentrosomal microtubule; EB1; DYNAMICS; ORGANIZATION; PROTEIN; FUSION; COMPLEXES; HOMOLOG; TUBULIN; HEALTH; ROLES;
D O I
10.1002/1873-3468.12758
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
Microtubules (MTs) play essential roles in many steps of autophagy, an important degradation pathway in the maintenance of cellular homoeostasis. In many cells, MT networks are comprised of centrosomal MTs and noncentrosomal MTs. However, it is unknown whether noncentrosomal MTs and its binding proteins are involved in autophagy. Here, we show in HeLa cells that calmodulin-regulated spectrin-associated protein 2 (CAMSAP2), a noncentrosomal MT minus-end stabilizing protein, regulates retrograde transport of autophagosomes through MT dynamics. CAMSAP2 cooperates with EB1 to regulate end-binding protein 1 (EB1) behaviour at MT plus ends, MT growth directions and autophagosome transport. An association between CAMSAP2 and EB1 in the cytosol may modulate EB1 binding to MT plus ends. Collectively, our data indicate that noncentrosomal MTs regulate autophagy through a cross-talk between CAMSAP2 and EB1.
引用
收藏
页码:2379 / 2393
页数:15
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