The Journal of Experimental Medicine
Avanti Polar Lipids, Inc.
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

Published online 20 November 2006 doi:10.1084/jem.20312iti4
Rockefeller University Press, 0022-1007 $8.00
JEM, Volume 203, Number 12, 2567-2567
This Article
Right arrow Full Text (PDF, 829K)
Right arrow PPT slides of all figures
Right arrow Alert me when this article is cited
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Alert me to new content in the JEM
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Williams, R.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Williams, R.
Related Collections
Right arrowRelated Article
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

IN THIS ISSUE

Reducing cell–cell stickiness with JAM-C

Figure 1
JAM-C (green) loosens cell junctions (red) to increase blood vessel permeability.

Most cell junction proteins increase endothelial cell–cell adhesion. But junction adhesion molecule-C (JAM-C), despite its sticky name, loosens vascular endothelial cell connections, thus allowing increased blood vessel permeability.

Increasing the permeability of small blood vessels is essential for new vessels to form and for leukocytes to escape the circulation and enter surrounding tissues during inflammation and tissue repair. Permeability is thought to be controlled by tight junctions between neighboring cells. Most tight junction components promote cell–cell adhesion and thus reduce permeability. But Orlova et al. (page 2703) show that the tight junction protein JAM-C does the opposite—it promotes permeability. Indeed JAM-C is the first junctional molecule reported to behave this way.

Using dye tracking, the team showed that knocking down JAM-C reduced endothelial permeability both in vitro and in vivo. The permeability-promoting effect of JAM-C was not on tight junctions themselves, but rather on a different type of cell–cell junction called adherens junctions, which contain the adhesion protein VE-cadherin. Knocking down JAM-C led to increased adhesion between VE-cadherin molecules at cell junctions. Such increased interaction is thought to trigger, via junction-associated factors, a series of steps that ultimately promotes actin depolymerization—thus further reducing permeability, as cells are unable to contract and pull apart. Consistent with this theory, knocking down JAM-C also reduced intracellular actin polymerization.

That a molecule from one type of junction can promote permeability by acting on another type of junction was surprising. The team found, however, that JAM-C increased endothelium permeability whether located at the cell junctions or diffusely distributed in the cytoplasm, indicating that JAM-C might be a signaling as well as structural protein, though the authors have yet to investigate this possibility.

One of the many more typical tight junction molecules that reduce vessel permeability is JAM-A, a closely related family member of JAM-C. How two such structurally similar junction molecules can have opposing effects on blood vessel permeability remains to be determined. Formula



Ruth Williams

ruth.williams{at}rockefeller.edu


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

Related Article

Junctional adhesion molecule-C regulates vascular endothelial permeability by modulating VE-cadherin–mediated cell–cell contacts
Valeria V. Orlova, Matina Economopoulou, Florea Lupu, Sentot Santoso, and Triantafyllos Chavakis
J. Exp. Med. 2006 203: 2703-2714. [Abstract] [Full Text] [PDF]




This Article
Right arrow Full Text (PDF, 829K)
Right arrow PPT slides of all figures
Right arrow Alert me when this article is cited
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Alert me to new content in the JEM
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Williams, R.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Williams, R.
Related Collections
Right arrowRelated Article
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?


  Home | Help | Feedback | Subscriptions | Archive | Search
TABLE OF CONTENTS