Literature DB >> 30011599

Unified biophysical mechanism for cell-shape oscillations and cell ingression.

Wei-Chang Lo1, Craig Madrak1, Daniel P Kiehart2, Glenn S Edwards1.   

Abstract

We describe a mechanochemical and percolation cascade that augments myosin's regulatory network to tune cytoskeletal forces. Actomyosin forces collectively generate cytoskeletal forces during cell oscillations and ingression, which we quantify by elastic percolation of the internally driven, cross-linked actin network. Contractile units can produce relatively large, oscillatory forces that disrupt crosslinks to reduce cytoskeletal forces. A (reverse) Hopf bifurcation switches contractile units to produce smaller, steady forces that enhance crosslinking and consequently boost cytoskeletal forces to promote ingression. We describe cell-shape changes and cell ingression in terms of intercellular force imbalances along common cell junctions.

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Year:  2018        PMID: 30011599      PMCID: PMC6440536          DOI: 10.1103/PhysRevE.97.062414

Source DB:  PubMed          Journal:  Phys Rev E        ISSN: 2470-0045            Impact factor:   2.529


  2 in total

Review 1.  Mathematical models of dorsal closure.

Authors:  A C Aristotelous; J M Crawford; G S Edwards; D P Kiehart; S Venakides
Journal:  Prog Biophys Mol Biol       Date:  2018-05-29       Impact factor: 3.667

2.  Elasticity, Stability, and Quasioscillations of Cell-Cell Junctions in Solid Confluent Epithelia.

Authors:  Clément Zankoc; Matej Krajnc
Journal:  Biophys J       Date:  2020-10-02       Impact factor: 4.033

  2 in total

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