| Literature DB >> 33207224 |
Jonathon M Muncie1, Nadia M E Ayad1, Johnathon N Lakins2, Xufeng Xue3, Jianping Fu4, Valerie M Weaver5.
Abstract
Embryogenesis is directed by morphogens that induce differentiation within a defined tissue geometry. Tissue organization is mediated by cell-cell and cell-extracellular matrix (ECM) adhesions and is modulated by cell tension and tissue-level forces. Whether cell tension regulates development by modifying morphogen signaling is less clear. Human embryonic stem cells (hESCs) exhibit an intrinsic capacity for self-organization, which motivates their use as a tractable model of early human embryogenesis. We engineered patterned substrates that recapitulate the biophysical properties of the early embryo and mediate the self-organization of "gastrulation-like" nodes in cultured hESCs. Tissue geometries that generated local nodes of high cell-adhesion tension directed the spatial patterning of the BMP4-dependent "gastrulation-like" phenotype by enhancing phosphorylation and junctional release of β-catenin to promote Wnt signaling and mesoderm specification. Furthermore, direct force application via mechanical stretching promoted BMP-dependent mesoderm specification, confirming that tissue-level forces can directly regulate cell fate specification in early human development.Entities:
Keywords: cytoskeletal tension; gastrulation; human embryonic stem cells; mesoderm; polyacrylamide hydrogels; self-organization; tissue patterning; traction force microscopy
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Year: 2020 PMID: 33207224 PMCID: PMC7755684 DOI: 10.1016/j.devcel.2020.10.015
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270