Mechanical Tension Promotes Formation of Gastrulation-like Nodes and Patterns Mesoderm Specification in Human Embryonic Stem Cells

Dev Cell. 2020 Dec 21;55(6):679-694.e11. doi: 10.1016/j.devcel.2020.10.015. Epub 2020 Nov 17.

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.

Keywords: cytoskeletal tension; gastrulation; human embryonic stem cells; mesoderm; polyacrylamide hydrogels; self-organization; tissue patterning; traction force microscopy.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Bone Morphogenetic Protein 4 / metabolism
  • Cell Differentiation*
  • Cells, Cultured
  • Gastrulation*
  • HEK293 Cells
  • Human Embryonic Stem Cells / cytology*
  • Human Embryonic Stem Cells / metabolism
  • Humans
  • Mesoderm / cytology*
  • Mice
  • Stress, Mechanical*
  • Wnt Signaling Pathway
  • beta Catenin / metabolism

Substances

  • BMP4 protein, human
  • Bone Morphogenetic Protein 4
  • beta Catenin