How autophagy both activates and inhibits cellular senescence

被引:203
作者
Kang, Chanhee [1 ]
Elledge, Stephen J. [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Dept Genet, Med Sch,Div Genet,Howard Hughes Med Inst, Boston, MA 02115 USA
关键词
Cellular senescence; DNA damage response (DDR); GATA4; selective autophagy; senescence-associated secretory phenotype (SASP); SQSTM1/p62;
D O I
10.1080/15548627.2015.1121361
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Autophagy and cellular senescence are stress responses essential for homeostasis. While recent studies indicate a genetic relationship between autophagy and senescence, whether autophagy acts positively or negatively on senescence is still subject to debate. Although autophagy was originally recognized as a nonspecific lysosomal degradation pathway (general autophagy), increasing evidence supports a selective form of autophagy that mediates the degradation of specific targets (selective autophagy). Our recent study revealed distinctive roles of selective autophagy and general autophagy in the regulation of senescence, at least in part resolving apparently contradictory reports regarding the relationship between these 2 important homeostatic stress responses.
引用
收藏
页码:898 / 899
页数:2
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