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Plexin-B2 orchestrates collective stem cell dynamics via actomyosin contractility, cytoskeletal tension and adhesion.
- Source :
-
Nature communications [Nat Commun] 2021 Oct 14; Vol. 12 (1), pp. 6019. Date of Electronic Publication: 2021 Oct 14. - Publication Year :
- 2021
-
Abstract
- During morphogenesis, molecular mechanisms that orchestrate biomechanical dynamics across cells remain unclear. Here, we show a role of guidance receptor Plexin-B2 in organizing actomyosin network and adhesion complexes during multicellular development of human embryonic stem cells and neuroprogenitor cells. Plexin-B2 manipulations affect actomyosin contractility, leading to changes in cell stiffness and cytoskeletal tension, as well as cell-cell and cell-matrix adhesion. We have delineated the functional domains of Plexin-B2, RAP1/2 effectors, and the signaling association with ERK1/2, calcium activation, and YAP mechanosensor, thus providing a mechanistic link between Plexin-B2-mediated cytoskeletal tension and stem cell physiology. Plexin-B2-deficient stem cells exhibit premature lineage commitment, and a balanced level of Plexin-B2 activity is critical for maintaining cytoarchitectural integrity of the developing neuroepithelium, as modeled in cerebral organoids. Our studies thus establish a significant function of Plexin-B2 in orchestrating cytoskeletal tension and cell-cell/cell-matrix adhesion, therefore solidifying the importance of collective cell mechanics in governing stem cell physiology and tissue morphogenesis.<br /> (© 2021. The Author(s).)
- Subjects :
- Actins
CRISPR-Cas Systems
Cell Differentiation
Cell-Matrix Junctions metabolism
Embryonic Stem Cells
Gene Editing
Gene Expression
Humans
Mechanotransduction, Cellular
Morphogenesis
Neural Stem Cells
Semaphorins
Signal Transduction
Actomyosin metabolism
Cell Adhesion physiology
Cytoskeleton metabolism
Nerve Tissue Proteins genetics
Nerve Tissue Proteins metabolism
Stem Cells metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 12
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 34650052
- Full Text :
- https://doi.org/10.1038/s41467-021-26296-7