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Updated: Aug 6, 2026

Analysis of Protein-protein Interactions and Co-localization Between Components of Gap, Tight, and Adherens Junctions in Murine Mammary Glands
Published on: May 30, 2017
Junctional Adhesion Molecules (JAMs) are differentially expressed in fibroblasts and co-localize with ZO-1 to
Andrew P Morris1, Ahmad Tawil, Zuzana Berkova
1Department of Integrative Biology and Pharmacology, University of Texas at Houston Medical School, Houston, Texas 77030, USA.
Insights
Junctional Adhesion Molecules (JAMs) are present in fibroblast junctions, particularly JAM-C in dermal fibroblasts. This finding extends the known roles of JAMs beyond epithelial and endothelial cells into mesenchymal tissues.
Area of Science:
- Cell Biology
- Molecular Biology
- Biochemistry
Background:
- Junctional Adhesion Molecules (JAMs) are established regulators of epithelial and endothelial tight junctions.
- The molecular composition of fibroblast adherens-like junctions is not well-defined.
Purpose of the Study:
- To investigate the expression profiles of JAMs in various fibroblast cultures.
- To determine the role of JAMs in fibroblast cell-cell adhesion.
Main Methods:
- Immunostaining of primary human and murine fibroblast cultures.
- Co-localization studies with ZO-1, N-Cadherin, and Cadherin-11.
Main Results:
- JAM-C was identified in human dermal, lung, and corneal fibroblasts.
- JAM-A and JAM-C were found in different murine fibroblast lines.
- In dermal fibroblasts, JAM-C localized to adherens-like junctions, co-localizing with ZO-1, N-Cadherin, and Cadherin-11.
Conclusions:
- Endogenous JAM-C is a component of dermal fibroblast adherens-like junctions.
- JAM expression and function extend to mesenchymal tissues, broadening their known biological roles.
Abstract:
Junctional Adhesion Molecules (JAMs) are components and regulators of the well-characterized epithelial and endothelial tight junction. Since the molecular components of native fibroblast adherens-like junctions remain poorly described we determined JAM expression profiles in fibroblasts. We found JAM-C on human dermal, lung, and corneal primary fibroblast cultures. Within murine lines, JAM-A was found in L-cells, JAM-C in 3T3 L1 cells, and both JAM-A and JAM-C were co-expressed in NIH 3T3 fibroblasts. In primary dermal fibroblasts, JAM-C concentrated at zipper-like junctions that formed between apposing cells. Dual immunostaining showed JAM-C co-localization with the ZO-1 intracellular scaffolding molecule at cell contacts that ranged from 7 microm to over 25 microm in length. JAM-C also labeled similar zipper-like junctions detected with N-Cadherin and Cadherin-11 antibodies. We conclude that endogenous JAM-C is an integral component of the dermal fibroblast adherens-like junction, and our data extend the expression and potential function of JAMs into mesenchymal tissues.
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