Gene regulatory programmes of tissue regeneration

被引:127
作者
Goldman, Joseph A. [1 ]
Poss, Kenneth D. [2 ,3 ]
机构
[1] Ohio State Univ, Dept Biol Chem & Pharmacol, Columbus, OH 43210 USA
[2] Duke Univ, Regenerat Next, Durham, NC 27708 USA
[3] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
基金
美国国家卫生研究院;
关键词
ZEBRAFISH HEART REGENERATION; ADULT STEM-CELLS; CARDIOMYOCYTE PROLIFERATION; PHASE-SEPARATION; TRANSCRIPTION FACTORS; NEURONAL PROGENITORS; LIMB REGENERATION; MULLER GLIA; BETA-CELLS; EXPRESSION;
D O I
10.1038/s41576-020-0239-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Regeneration is the process by which organisms replace lost or damaged tissue, and regenerative capacity can vary greatly among species, tissues and life stages. Tissue regeneration shares certain hallmarks of embryonic development, in that lineage-specific factors can be repurposed upon injury to initiate morphogenesis; however, many differences exist between regeneration and embryogenesis. Recent studies of regenerating tissues in laboratory model organisms - such as acoel worms, frogs, fish and mice - have revealed that chromatin structure, dedicated enhancers and transcriptional networks are regulated in a context-specific manner to control key gene expression programmes. A deeper mechanistic understanding of the gene regulatory networks of regeneration pathways might ultimately enable their targeted reactivation as a means to treat human injuries and degenerative diseases. In this Review, we consider the regeneration of body parts across a range of tissues and species to explore common themes and potentially exploitable elements. The capacity to regenerate tissue varies across different species and tissue types. The poor regenerative capacity of organs such as the heart and nervous system contributes to the aetiology of a number of serious diseases, including heart failure and Alzheimer disease. In this Review, Goldman and Poss discuss how genetic programmes of regeneration are regulated and how the control mechanisms might be adapted to treat human disease.
引用
收藏
页码:511 / 525
页数:15
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