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

Published online 3 May 2004. doi:10.1083/jcb1653rr1
The Rockefeller University Press, 0021-9525 $8.00
JCB, Volume 165, Number 3, 296-296
This Article
Right arrow Full Text (PDF, 699K)
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 LeBrasseur, N.
Right arrow Search for Related Content
PubMed
Right arrow Articles by LeBrasseur, N.
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?

Research Roundup

Intimacy is a cellular turn-on



The space (red) between cells gets cramped when pressure is applied (right).

Drazen/Macmillan

The simple act of coming closer together ignites signaling pathways in epithelial cells, as shown by Daniel Tschumperlin, Jeffrey Drazen (Harvard School of Public Health, Boston, MA), and colleagues. The results describe how cells might activate cellular responses to mechanical stress.

Cells are pushed closer together by physical forces. In the lung, for instance, epithelial cells feel the pressure from underlying muscle tissue, particularly in asthmatic patients. The authors see that these forces do not change cellular volume. Rather, they squeeze out fluids from between neighboring cells.

The resulting close cellular proximity means that ligands that get secreted between cells are more concentrated and therefore more likely to activate signaling pathways. "Now there's less space for these things to bounce around in before they find a receptor," says Tschumperlin.

Lung cells under mechanical stress phosphorylate ERK as a result of EGFR activation. The authors find that this phosphorylation is due to the HB-EGF ligand. Assuming that ligand secretion and diffusion rates are uniform, they calculate that ligand concentration is inversely proportional to the width of the space between cells. Putting their equation to the test, they found that stress, or an increase in ligand equivalent to that predicted from that stress, both activated ERK phosphorylation to the same extent.

"When we put our results together, it seemed so obvious that we had to go back to the literature to see why no one had suggested it before," says Tschumperlin. "No proteins or molecules or channels sensitive to stress are needed. Cells just use the existing machinery, not directly changing any proteins, in a changing extracellular volume."

This simple system may extend to any cell type that releases ligands into a restricted space. Proliferating cells that get more tightly packed during development, for example, might activate differentiation pathways at the right place and time. {blacksquare}

Reference:

Tschumperlin, D., et al. 2004. Nature. 10.1038/nature02543.



Nicole LeBrasseur

lebrasn{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, 699K)
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 LeBrasseur, N.
Right arrow Search for Related Content
PubMed
Right arrow Articles by LeBrasseur, N.
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