Auxetic nuclei in embryonic stem cells exiting pluripotency

被引:2
|
作者
Pagliara, Stefano [1 ]
Franze, Kristian [2 ]
McClain, Crystal R. [1 ,3 ,4 ]
Wylde, GeorgeW. [1 ]
Fisher, Cynthia L. [5 ]
Franklin, Robin J. M. [3 ,4 ]
Kabla, Alexandre J. [6 ]
Keyser, Ulrich F. [1 ]
Chalut, Kevin J. [1 ,5 ]
机构
[1] Univ Cambridge, Cavendish Lab, Dept Phys, Cambridge CB3 0HE, England
[2] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge CB2 3DY, England
[3] Univ Cambridge, Wellcome Trust, MRC, Cambridge Stem Cell Inst, Cambridge CB3 0ES, England
[4] Univ Cambridge, Dept Clin Neurosci, Cambridge CB3 0ES, England
[5] Univ Cambridge, Wellcome Trust, MRC, Cambridge Stem Cell Inst, Cambridge CB2 1QR, England
[6] Univ Cambridge, Dept Engn, Cambridge CB2 1PZ, England
基金
英国医学研究理事会; 欧洲研究理事会; 英国惠康基金;
关键词
ATOMIC-FORCE MICROSCOPY; CHROMATIN DECONDENSATION; VISCOELASTIC PROPERTIES; GROUND-STATE; DIFFERENTIATION; PLASTICITY; DYNAMICS; CULTURE;
D O I
10.1038/NMAT3943
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Embryonic stem cells (ESCs) self-renew in a state of naive pluripotency in which they are competent to generate all somatic cells. It has been hypothesized that, before irreversibly committing, ESCs pass through at least one metastable transition state. This transition would represent a gateway for differentiation and reprogramming of somatic cells. Here, we show that during the transition, the nuclei of ESCs are auxetic: they exhibit a cross-sectional expansion when stretched and a cross-sectional contraction when compressed, and their stiffness increases under compression. We also show that the auxetic phenotype of transition ESC nuclei is driven at least in part by global chromatin decondensation. Through the regulation of molecular turnover in the differentiating nucleus by external forces, auxeticity could be a key element in mechanotransduction. Our findings highlight the importance of nuclear structure in the regulation of differentiation and reprogramming.
引用
收藏
页码:638 / 644
页数:7
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