Epithelial to mesenchymal transition as a portal to stem cell characters embedded in gene networks

被引:13
作者
Asli, Naisana S. [1 ,2 ]
Harvey, Richard P. [1 ,2 ,3 ]
机构
[1] Victor Chang Cardiac Res Inst, Darlinghurst, NSW, Australia
[2] Univ New S Wales, St Vincents Clin Sch, Kensington, NSW 2033, Australia
[3] Univ Melbourne, Melbourne, Vic 3010, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
epicardium; epithelial to mesenchymal transition; heart regeneration; reprogramming; stem cells; BREAST-CANCER; HUMAN FIBROBLASTS; E-CADHERIN; TRANSCRIPTIONAL REPRESSOR; HEART REGENERATION; EPICARDIAL CELLS; SNAIL; SLUG; RESISTANCE; MOUSE;
D O I
10.1002/bies.201200089
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
Cells can transit between a range of stable epithelial and mesenchymal states and this has allowed the evolution of complex body forms. Epithelial to mesenchymal transition (EMT) and its reverse, mesenchymal to epithelial transition (MET), occur sequentially in development and organogenesis. EMT often accompanies transitions between stem-like cells and their more differentiated progeny, as occurs at gastrulation, although the relevance of this had not been clarified. New findings from the cancer and cell reprogramming fields suggest that EMT and MET can act as essential portals to stem cell character. Here, we review these findings in the broader context of EMT and MET with emphasis on stem cell biology. Using the heart as an example, we also explore the potential role of EMT/MET in organ regeneration. Understanding EMT and MET at a network level will give us new tools to probe stem cell character and enhance tissue repair.
引用
收藏
页码:191 / 200
页数:10
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