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

Published online 29 July 2002. doi:10.1083/jcb1583rr2
This Article
Right arrow Full Text (PDF, 202K)
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?

© The Rockefeller University Press, 0021-9525/2002/8/384-a $5.00
The Journal of Cell Biology, Volume 158, Number 3, August 5, 2002 384-a-384


Research Roundup

Active cells choose life


Macrophages bind to all neutrophils at 20°C, but viable ones escape at 37°C.

Brown/Macmillan

When macrophages perform their search-and-destroy missions, it is not simply up to apoptotic cells to flag down their destroyers. New results from Simon Brown (University of Edinburgh, Edinburgh, UK) and colleagues reveal that viable cells must actively avoid engulfment by phagocytes. A single cell adhesion molecule, CD31, can lead to either engulfment or escape.Brown and his colleagues found CD31 by purifying proteins involved in tethering of cells to macrophages at low temperatures, when phagocytosis and cytoskeletal rearrangements were inhibited. Both viable and apoptotic leukocytes bound to macrophages through homophilic CD31 interactions. At 37°C, however, this interaction was transient for viable leukocytes. The cytoplasmic portion of CD31 imparted these cells with the ability to avoid destruction by actively promoting detachment from the macrophages. Apopotic cells had somehow lost this capability.

"‘Eat-me signals’ are what are usually looked for, but we found ‘don’t-eat-me signals' instead," says Brown. "It would seem more efficient for an apoptotic cell to lose a signaling ability than gain one." In this way, and by ligating self-recognition receptors, macrophages can determine whether a cell has lost its ability to respond to external signals and is thus ready for disposal. Whether viable cells actively escape from macrophages either by activating motility machinery (as happens upon CD31 ligation between leukocytes and endothelial cells) or by inhibiting subsequent interactions between the target and the macrophage is the focus of continuing studies. {blacksquare}

Reference:

Brown, S., et al. 2002. Nature. 418:200–203.[CrossRef][Medline]



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, 202K)
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