JCB logo
amgmicro.com
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

Published online 27 January 2003. doi:10.1083/jcb1603rr5
This Article
Right arrow Full Text (PDF, 581K)
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 JCB
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 Wells, W. A.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Wells, W. A.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

© The Rockefeller University Press, 0021-9525/2003/2/287-b $5.00
The Journal of Cell Biology, Volume 160, Number 3, 287-b-287


Research Roundup

Poised to migrate


Epithelial cells (green) go for a walk when Moesin is missing (right).

Fehon/Macmillan

Epithelial cells are ready to run off at any moment, at least based on the results of Olga Speck, Richard Fehon (Duke University, Durham, NC), and colleagues. They have found that moesin, previously thought to be a stolid structural component, is actually a signaling protein that maintains epithelial cell identity by suppressing Rho activity.

Ezrin, radixin, and moesin (ERM)—represented only by Moesin in flies—are proteins that link actin to various transmembrane proteins at the apical surface of epithelial cells. The link was thought to help maintain epithelial structures such as microvilli, but Fehon's group found that flies lacking Moesin had epithelial cells that lost polarity, dropped out of monolayers, and migrated invasively.

Moesin appears to act by suppressing Rho. Interfering with ERM proteins in mammalian epithelial cells boosted Rho activity, and fly Moesin mutants improved when Rho1 dose was halved. Rho1 overexpression in wild type, however, phenocopied Moesin loss.Thus epithelial cells must be actively maintained in their polarized state, lest they slip off into the motile night. This instability may reflect the transitions from structured epithelium to motile founder cells that occur frequently during development—a transition that carcinoma cells apparently recapitulate when they become metastatic. {blacksquare}

Reference:

Speck, O., et al. 2003. Nature. 421:83–87.[CrossRef][Medline]



William A. Wells

wellsw{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 Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?



This Article
Right arrow Full Text (PDF, 581K)
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 JCB
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 Wells, W. A.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Wells, W. A.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?


  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents