Autophagy is required for zebrafish caudal fin regeneration

被引:69
|
作者
Varga, M. [1 ]
Sass, M. [2 ]
Papp, D. [1 ]
Takacs-Vellai, K. [1 ]
Kobolak, J. [3 ]
Dinnyes, A. [3 ]
Klionsky, D. J. [4 ]
Vellai, T. [1 ]
机构
[1] Eotvos Lorand Univ, Dept Genet, Budapest, Hungary
[2] Eotvos Lorand Univ, Dept Anat Cell & Dev Biol, Budapest, Hungary
[3] BioTalentum Ltd, H-2100 Godollo, Hungary
[4] Univ Michigan, Inst Life Sci, Ann Arbor, MI 48109 USA
来源
CELL DEATH AND DIFFERENTIATION | 2014年 / 21卷 / 04期
关键词
autophagy; regeneration; zebrafish; differentiation; cell death; HEART REGENERATION; DEDIFFERENTIATION; MECHANISMS; BLASTEMA; INHIBITION; EXPRESSION; INDUCTION; CAPACITY; SURVIVAL; GROWTH;
D O I
10.1038/cdd.2013.175
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
Regeneration is the ability of multicellular organisms to replace damaged tissues and regrow lost body parts. This process relies on cell fate transformation that involves changes in gene expression as well as in the composition of the cytoplasmic compartment, and exhibits a characteristic age-related decline. Here, we present evidence that genetic and pharmacological inhibition of autophagy - a lysosome-mediated self-degradation process of eukaryotic cells, which has been implicated in extensive cellular remodelling and aging - impairs the regeneration of amputated caudal fins in the zebrafish (Danio rerio). Thus, autophagy is required for injury-induced tissue renewal. We further show that upregulation of autophagy in the regeneration zone occurs downstream of mitogen-activated protein kinase/extracellular signal-regulated kinase signalling to protect cells from undergoing apoptosis and enable cytosolic restructuring underlying terminal cell fate determination. This novel cellular function of the autophagic process in regeneration implies that the role of cellular self-digestion in differentiation and tissue patterning is more fundamental than previously thought.
引用
收藏
页码:547 / 556
页数:10
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