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Updated: May 25, 2026

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Triggering a cell shape change by exploiting preexisting actomyosin contractions.

Minna Roh-Johnson1, Gidi Shemer, Christopher D Higgins

  • 1Department of Biology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.

Science (New York, N.Y.)
|February 11, 2012
PubMed
Summary
This summary is machine-generated.

Apical constriction, crucial for development, is triggered by linking cell contacts to the actomyosin cortex, not by changes in cortical tension. This finding clarifies cell shape changes during morphogenesis.

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Area of Science:

  • Cell biology
  • Developmental biology
  • Biophysics

Background:

  • Apical constriction drives key morphogenetic events like gastrulation and neural tube closure.
  • It is traditionally thought to be initiated by actomyosin network contractions.
  • Understanding the precise triggers of apical constriction is vital for developmental biology.

Purpose of the Study:

  • To investigate the initial triggers of apical constriction.
  • To differentiate between cortical tension changes and cell-cell contact dynamics in initiating apical constriction.
  • To elucidate the spatiotemporal relationship between actomyosin activity and cell shape change.

Main Methods:

  • Comparative study in Caenorhabditis elegans and Drosophila.
  • Observation of actomyosin network dynamics and cortical tension.
  • Analysis of apical cell-cell contact zone behavior.
  • Live imaging and biophysical measurements.

Main Results:

  • Apical actomyosin contractions precede observable cell shape changes in both model organisms.
  • Initially, actomyosin networks contract dynamically, generating cortical tension without significant apical surface area reduction.
  • Apical cell-cell contact zones and actomyosin subsequently move together, without altered actomyosin dynamics or cortical tension.

Conclusions:

  • Apical constriction is initiated by the dynamic linkage of apical cell-cell contacts to an already contractile actomyosin cortex.
  • The trigger is not a change in cortical tension, but the coordinated coupling of cellular interfaces.
  • This mechanism provides new insights into the regulation of cell shape during embryonic development.