Coordination of Morphogenesis and Cell-Fate Specification in Development

被引:128
|
作者
Chan, Chii J. [1 ]
Heisenberg, Carl-Philipp [2 ]
Hiiragi, Takashi [1 ]
机构
[1] European Mol Biol Lab, D-69117 Heidelberg, Germany
[2] IST Austria, A-3400 Klosterneuburg, Austria
关键词
LIVING EMBRYONIC-TISSUES; BRILLOUIN MICROSCOPY; MOUSE BLASTOCYST; LINEAGE SEGREGATION; SELF-ORGANIZATION; MECHANICAL FORCES; FLUID FORCES; NODAL FLOW; STEM-CELLS; MECHANOTRANSDUCTION;
D O I
10.1016/j.cub.2017.07.010
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
During animal development, cell-fate-specific changes in gene expression can modify the material properties of a tissue and drive tissue morphogenesis. While mechanistic insights into the genetic control of tissueshaping events are beginning to emerge, how tissue morphogenesis and mechanics can reciprocally impact cell-fate specification remains relatively unexplored. Here we review recent findings reporting how multicellular morphogenetic events and their underlying mechanical forces can feed back into gene regulatory pathways to specify cell fate. We further discuss emerging techniques that allow for the direct measurement and manipulation of mechanical signals in vivo, offering unprecedented access to study mechanotransduction during development. Examination of the mechanical control of cell fate during tissue morphogenesis will pave the way to an integrated understanding of the design principles that underlie robust tissue patterning in embryonic development.
引用
收藏
页码:R1024 / R1035
页数:12
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