JCB logo
R&D Systems
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

Published online February 25, 2008
doi:10.1083/jcb.1805rr2
The Journal of Cell Biology, Vol. 180, No. 5, 849-
The Rockefeller University Press, 0021-9525 $30.00
© 2008 LeBrasseur
This Article
Right arrow PDF (Full Text)
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 Reddit   Add to Technorati  
What's this?

Research Roundup

Sopping up chemokine


Figure 1
Primordial germ cells (in circles) avoid CXCR7 (blue), which soaks up SDF-1 guidance cues.

SMALL/MACMILLAN

Asponge-like receptor sops up excess chemokine to refine the path for migrating primordial germ cells, based on findings from Bijan Boldajipour, Harsha Mahabaleshwar, Erez Raz (Center for Molecular Biology of Inflammation, Münster, Germany), and colleagues.

During development, germ cell precursors are drawn by gradients of the SDF-1 chemokine toward the gonads, where they will form the germ line. Zebrafish embryos have two SDF-1 receptors, CXCR4b and CXCR7, but the new results reveal that only CXCR4b leads the germ cells directly. CXCR7 was instead found on surrounding somatic cells, where it soaked up SDF-1.

The CXCR7 receptor and its bound SDF-1 ligand were taken into cells in endosomes. Rather than activate migratory signaling pathways, the receptor simply seemed to bring its ligand to lysosomes, where it is probably degraded.

Migrating germ cells avoided regions where CXCR7 sopped up SDF-1. The group suspects that the intake by CXCR7 allows conversion of the changes in SDF-1 mRNA expression patterns into differences in the protein pattern.

"To begin with," says Raz, "SDF-1 is expressed broadly throughout the embryo," drawing in the widely dispersed precursors. As development proceeds, he says, "SDF-1 expression becomes more restricted, and the old info must be quickly erased as cells draw nearer to their destination. If the ligand isn't cleared, it will reach unusually high levels, and the gradient will be disturbed." Such problems were seen in embryos lacking CXCR7, in which germ cells were unable to polarize or migrate. They were similarly immobilized when extra SDF-1 was expressed throughout the embryo. Formula

Reference:

Boldajipour, B., et al. 2008. Cell. 132:463–473.[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 Reddit Reddit   Add to Technorati Technorati    What's this?



This Article
Right arrow PDF (Full Text)
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 Reddit   Add to Technorati  
What's this?


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