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Related Concept Videos

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Tight junctions are molecular seals between cells that prevent the leaking of fluids, ions, and other small solutes across cavities and compartments in multicellular organisms. They are mainly composed of claudin and occludin transmembrane proteins, and other proteins such as tricellulin and JAM (junctional adhesion molecule). All these proteins are 4-pass transmembrane proteins, except JAM, which is a single-pass transmembrane protein belonging to the immunoglobulin superfamily. The...
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Rapidly dividing tumors, embryos, and wounded tissues require more oxygen than usual, lowering the oxygen concentration in the blood. At low oxygen or hypoxic conditions, an oxygen-sensitive transcription factor called the hypoxia-inducible factor 1 or HIF1 is activated. HIF1 is a dimeric protein of alpha (ɑ) and beta (β) subunits.  Under optimal oxygen conditions, HIF1β is present in the nucleus while HIF1ɑ remains in the cytosol. HIF1ɑ is hydroxylated by prolyl...
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Related Experiment Video

Updated: Apr 7, 2026

An Intravital Microscopy-Based Approach to Assess Intestinal Permeability and Epithelial Cell Shedding Performance
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Gap geometry dictates epithelial closure efficiency.

Andrea Ravasio1, Ibrahim Cheddadi2, Tianchi Chen1

  • 1Mechanobiology Institute, National University of Singapore, Singapore 117411, Singapore.

Nature Communications
|July 10, 2015
PubMed
Summary
This summary is machine-generated.

Epithelial tissue repair relies on cell crawling and actomyosin cable constriction, with gap geometry dictating their interplay. Mechanical coupling between these processes ensures efficient wound closure and tissue integrity restoration.

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Area of Science:

  • Cell biology
  • Biophysics
  • Developmental biology

Background:

  • Tissue integrity is crucial for multicellular organisms.
  • Misregulated tissue repair can cause inflammation and cancer.
  • Epithelial cells use crawling and actomyosin cable constriction to close gaps.

Purpose of the Study:

  • To investigate how epithelial gap geometry influences collective cell motion.
  • To elucidate the mechanical coupling between cell crawling and actomyosin cable contraction.
  • To model the roles of these mechanisms in tissue repair.

Main Methods:

  • In vitro and in vivo experiments on epithelial gap closure.
  • Analysis of collective cell migration dynamics.
  • Computational modeling of tissue repair mechanisms.

Main Results:

  • Epithelial gap geometry is a key regulator of cell crawling and actomyosin cable constriction.
  • Mechanical coupling between these two processes controls large-scale gap closure dynamics.
  • Computational models successfully clarified the distinct roles of each mechanism.

Conclusions:

  • A robust and universal mechanism for epithelial tissue repair has been identified.
  • Understanding this coupling provides insights into development and disease.
  • Gap geometry and mechanical feedback are critical for restoring tissue integrity.