Sirt1 promotes tissue regeneration in zebrafish through regulating the mitochondrial unfolded protein response

被引:13
|
作者
Lin, Yi-Fa [1 ,2 ,3 ]
Sam, Jessica [1 ]
Evans, Todd [1 ]
机构
[1] Weill Cornell Med, Dept Surg, 1300 York Ave,LC-708, New York, NY 10065 USA
[2] Natl Tsing Hua Univ, Inst Biotechnol, Hsinchu 30013, Taiwan
[3] Natl Tsing Hua Univ, Dept Life Sci, Hsinchu 30013, Taiwan
关键词
STRESS-RESPONSE; FIN; UPR; NICOTINAMIDE; HEART; MECHANISMS; AGE;
D O I
10.1016/j.isci.2021.103118
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mitochondrial unfolded protein response (UPRmt) is an organellar stress signaling pathway that functions to detect and restore disruption of mitochondrial proteostasis. The UPRmt is involved in a wide range of physiological and disease conditions, including aging, stem cell maintenance, innate immunity, neurodegeneration, and cancer. Here we report that the UPRmt is integral to zebrafish fin regeneration. Taking advantage of a novel zebrafish UPRmt reporter, we observed that UPRmt activation occurs in regenerating fin tissue shortly after injury. Through chemical and genetic approaches, we discovered that the Sirt1UPR(mt) pathway, best known for its role in promoting lifespan extension, is crucial for fin regeneration. The metabolism of NAD(+) is an important contributor to Sirt1 activity in this context. We propose that Sirt1 activation induces mitochondrial biogenesis in injured fin tissue, which leads to UPRmt activation and promotes tissue regeneration.
引用
收藏
页数:17
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