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Modeling cell proliferation for simulating three-dimensional tissue morphogenesis based on a reversible network

Satoru Okuda1, Yasuhiro Inoue, Mototsugu Eiraku

  • 1Department of Biomechanics, Institute for Frontier Medical Sciences, Kyoto University, 53 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto, 606-8507, Japan.

Biomechanics and Modeling in Mechanobiology
|December 1, 2012
PubMed
Summary
This summary is machine-generated.

This study models cell proliferation within a reversible network reconnection (RNR) framework, simulating tissue morphogenesis. The model accurately captures cell division and growth, influencing tissue size and shape.

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Area of Science:

  • Computational Biology
  • Developmental Biology
  • Biophysics

Background:

  • Tissue morphogenesis relies on cell proliferation, including cell division and growth.
  • Multicellular dynamics regulate these behaviors to achieve proper tissue size and shape in 3D.
  • The reversible network reconnection (RNR) model represents cell shapes as polyhedra for analyzing multicellular dynamics.

Purpose of the Study:

  • To extend the RNR model to simulate tissue morphogenesis incorporating proliferative cell behaviors.
  • To model cell division and growth within the RNR framework.

Main Methods:

  • Cell division modeled by polyhedron division via a planar surface, defined by timing, position, and orientation.
  • Cell growth modeled as volume increase based on individual cell cycle time.
  • Numerical simulations performed using the proposed RNR model framework.

Main Results:

  • Simulations demonstrated tissue growth through successive cell divisions over multiple cell cycles.
  • The model maintained individual cell size and shape while increasing cell number.
  • Tissue morphology was significantly altered by varying cell division plane orientations.

Conclusions:

  • The proposed RNR model framework successfully incorporates and expresses proliferative cell behaviors during morphogenesis.
  • This model provides a basis for simulating and understanding how cell division and growth dynamics shape tissues.