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Related Concept Videos

Cadherins in Tissue Organization01:19

Cadherins in Tissue Organization

The cadherins are a superfamily of cell adhesion molecules comprising over 180 variants, with specific tissues expressing a particular combination of cadherin types. Cadherins generally exhibit homophilic binding; i.e., cadherins on one cell bind to cadherins of the same or closely related type on another cell. Thus, cells of the same type have a specific affinity to bind to each other and sort themselves into clusters to form tissues.
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Structure of Cadherins01:25

Structure of Cadherins

The cadherins were one of the first cell adhesion molecules discovered; the term “cadherins”   is based on their calcium-dependent adhering properties. The first cadherins discovered on the epithelial, neuronal, and placental cells were named E-cadherin, P-cadherin, and N-cadherin, respectively. These classical cadherins share sequence and structural similarities. Other cadherins, including those involved in cell signaling, are grouped into non-classical cadherins. This diversity of cadherins...

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Enhancement of cell function through heterotypic cell-cell interactions using E-cadherin-expressing NIH3T3 cells.

Akira Ito1, Takehiko Kiyohara, Yoshinori Kawabe

  • 1Department of Chemical Engineering, Faculty of Engineering, Kyushu University, Fukuoka, Japan.

Journal of Bioscience and Bioengineering
|July 22, 2008
PubMed
Summary

Engineered E-cadherin in fibroblasts promoted cell-cell interactions with hepatocytes. This enhanced cell adhesion led to increased albumin secretion, suggesting a novel method for modulating cell function.

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Area of Science:

  • Cell Biology
  • Biochemistry
  • Molecular Biology

Background:

  • Epithelial (cell adhesion molecule) E-cadherin mediates cell-cell adhesion in epithelial tissues.
  • NIH3T3 fibroblasts were engineered to express E-cadherin to study its role in heterotypic cell interactions.

Purpose of the Study:

  • To investigate the impact of E-cadherin expression in fibroblasts on cell-cell interactions with other cell types.
  • To assess the functional consequences of engineered cell-cell contacts on hepatocyte function.

Main Methods:

  • NIH3T3 fibroblasts were genetically modified to express E-cadherin.
  • Co-culture experiments were performed between E-cadherin-expressing fibroblasts and rat hepatocytes.
  • Albumin secretion levels were measured as a functional indicator of hepatocyte activity.

Main Results:

  • Co-culturing E-cadherin-expressing fibroblasts with rat hepatocytes resulted in frequent and stable cell-cell contacts.
  • Enhanced albumin secretion was observed in hepatocytes when co-cultured with E-cadherin-expressing fibroblasts compared to controls.
  • The formation of heterotypic cell-cell interactions influenced hepatocyte function.

Conclusions:

  • E-cadherin expression in fibroblasts can effectively mediate cell-cell adhesion with hepatocytes.
  • Engineered cell-cell interactions can positively modulate hepatocyte function, specifically enhancing albumin secretion.
  • This study provides a model for understanding and potentially engineering cell-cell interactions for therapeutic or research applications.