Actin-myosin contractility is responsible for the reduced viability of dissociated human embryonic stem cells.

Actin-myosin contractility is responsible for the reduced viability of dissociated human embryonic stem cells.
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DOI:
10.1016/j.stem.2010.06.017
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发表时间:
2010-08-06
期刊:
影响因子:
23.9
通讯作者:
Thomson JA
Thomson JA
中科院分区:
医学1区
文献类型:
--
作者:
Chen G;Hou Z;Gulbranson DR;Thomson JA

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Human ES cells are the pluripotent precursor of the three embryonic germ layers. Human ES cells exhibit basal-apical polarity, junctional complexes, integrin-dependent matrix adhesion, and E-cadherin-dependent cell-cell adhesion, all characteristics shared by the epiblast epithelium of the intact mammalian embryo. After disruption of epithelial structures, programmed cell death is commonly observed. If individualized human ES cells are prevented from reattaching and forming colonies, their viability is significantly reduced. Here we show that actin-myosin contraction is a critical effector of the cell death response to human ES cell dissociation. Inhibition of myosin heavy chain ATPase, downregulation of myosin heavy chain, and downregulation of myosin light chain all increase survival and cloning efficiency of individualized human ES cells. ROCK inhibition decreases phosphorylation of myosin light chain, suggesting that inhibition of actin-myosin contraction is also the mechanism through which ROCK inhibitors increase cloning efficiency of human ES cells.
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