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

Published online 17 November 2003. doi:10.1083/jcb1634rr3
This Article
Right arrow Full Text (PDF, 391K)
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, 0021-9525/2003/11/691 $8.00
The Journal of Cell Biology, Volume 163, Number 4, 691-691


Research Roundup

Immune cells take in unknown enemies



Poliovirus RNA (white) still gets into APCs that lack the right receptor.

Freigang/NAS

MHC class I molecules normally present endogenously synthesized antigens and thus activate cytotoxic T lymphocytes (CTLs). In antigen- presenting cells (APCs), however, some seemingly extracellular antigens are cross-presented: they are loaded onto the class I pathway in addition to their usual presentation by MHC class II. For example, APCs in mice were recently shown to activate antipoliovirus CTLs, despite lacking a receptor for the virus, presumably by cross-presenting poliovirus antigens on class I. But now Stefan Freigang, Rolf Zinkernagel, and colleagues (University of Zurich, Zurich, Switzerland) show that the missing receptor does not stop viral uptake in APCs, suggesting that cross-presentation is not needed as an explanation.

"Even in a situation where everybody would suspect that cross-presentation is going on, we see that APCs are taking in the virus," says Freigang. His group finds viral RNA in APCs of the receptorless mice. Further, the RNA had to be translated to elicit CTL responses. Thus, even if cross-presentation—which does not require translation—might occur, it is too inefficient under physiological infection conditions to cause an immune response.

Not all cells are susceptible to viral infection, since only transgenic mice expressing the poliovirus receptor develop disease symptoms. So what is special about APCs is not clear. "We can only speculate on how the virus gets into the cell," says Freigang. Perhaps a subset of APCs has the ability to take in a variety of pathogens with a nonspecific receptor. {blacksquare}

Reference:

Freigang, S., et al. 2003. Proc. Natl. Acad. Sci. USA.. 10.1073/pnas.1835685100.



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, 391K)
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