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

Published online
doi:10.1083/jcb.1765rr1
The Journal of Cell Biology, Vol. 176, No. 5, 551-
The Rockefeller University Press, 0021-9525 $30.00
© Wells
This Article
Right arrow Full Text (PDF, 922K)
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?

Research Roundup

Chemokine blockade



Figure 1
D6 (black) protects placenta from invading chemokines.

MANTOVANI/NAS

A fetus must be sheltered from any inflammatory battle taking place in the mother. Now, Yeny Martinez de la Torre, Alberto Mantovani (University of Milan, Italy), and colleagues report that a decoy receptor in the placenta captures potentially dangerous pro-inflammatory chemokines from the mother. This scavenging suppresses inflammation and prevents fetal loss.

Decoy receptors such as the D6 receptor bind many inflammatory chemokines without activating intracellular signaling. Instead, the receptor and chemokine are internalized and the chemokine is destroyed.

The Italian group confirmed that D6 is expressed in the placenta, specifically on the apical side of syncytial trophoblasts. This is the side looking at the maternal blood and thus "a strategic location at the very interface between mother and fetus," says Mantovani.

To test the function of D6, the team injected pro-inflammatory LPS. The response was greater in mice lacking D6: several inflammatory chemokines built to higher levels in the circulation and placenta; more macrophages and T lymphocytes invaded the placenta; and there was more fetal loss.

Fetal loss may occur after a deadly positive feedback between inflammation and blood clotting in the placenta. In the mice lacking D6, this can be prevented with an infusion of anti-chemokine antibodies. A similar blocking approach may be possible in some humans who suffer from recurrent fetal loss, although it is not yet clear whether changes in D6 function are implicated in any of these individuals. Formula

Reference:

de la Torre, Y.M., et al. 2007. Proc. Natl. Acad. Sci. USA. doi:10.1073/pnas.0607514104.[Abstract/Free Full Text]



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, 922K)
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