Abscission Couples Cell Division to Embryonic Stem Cell Fate.

Abscission Couples Cell Division to Embryonic Stem Cell Fate.
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DOI:
10.1016/j.devcel.2020.09.001
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发表时间:
2020-10-26
期刊:
影响因子:
11.8
通讯作者:
Paluch EK
Paluch EK
中科院分区:
生物学1区
文献类型:
--
作者:
Chaigne A;Labouesse C;White IJ;Agnew M;Hannezo E;Chalut KJ;Paluch EK

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Cell fate transitions are key to development and homeostasis. It is thus essential to understand the cellular mechanisms controlling fate transitions. Cell division has been implicated in fate decisions in many stem cell types, including neuronal and epithelial progenitors. In other stem cells, such as embryonic stem (ES) cells, the role of division remains unclear. Here, we show that exit from naive pluripotency in mouse ES cells generally occurs after a division. We further show that exit timing is strongly correlated between sister cells, which remain connected by cytoplasmic bridges long after division, and that bridge abscission progressively accelerates as cells exit naive pluripotency. Finally, interfering with abscission impairs naive pluripotency exit, and artificially inducing abscission accelerates it. Altogether, our data indicate that a switch in the division machinery leading to faster abscission regulates pluripotency exit. Our study identifies abscission as a key cellular process coupling cell division to fate transitions. Mouse embryonic stem cells exit naive pluripotency after mitosis Naive embryonic stem cells display slow abscission and remain connected by bridges Cells exiting naive pluripotency display faster abscission Accelerating abscission facilitates exit from naive pluripotency Cell division has been implicated in fate decisions in many stem cells. Chaigne et al. show that mouse embryonic stem cells exit naive pluripotency after cell division. Naive sister cells remain connected by cytoplasmic bridges after division, and bridge abscission promotes naive pluripotency exit.
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