The Journal of Experimental Medicine
Torrey Pines Biolabs
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

Published 21 June 2004. doi:10.1084/jem.20032204
Rockefeller University Press, 0022-1007 $8.00
JEM, Volume 199, Number 12, 1719-1724
This Article
Right arrow Full Text
Right arrow Full Text (PDF, 145K)
Right arrow PPT slides of all figures
Right arrow Alert me when this article is cited
Right arrow Citation Map
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new content in the JEM
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Erman, B.
Right arrow Articles by Singer, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Erman, B.
Right arrow Articles by Singer, 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?

Brief Definitive Report

Defined {alpha}ß T Cell Receptors with Distinct Ligand Specificities Do Not Require Those Ligands to Signal Double Negative Thymocyte Differentiation

Batu Erman, Terry I. Guinter, and Alfred Singer

Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892

Address correspondence to Alfred Singer, Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Building 10, Room 4B36, Bethesda, MD 20892. Phone: (301) 496-5461; Fax: (301) 496-0887; email: SingerA{at}nih.gov

During T cell development in the thymus, pre–T cell receptor (TCR) complexes signal CD4 CD8 (double negative [DN]) thymocytes to differentiate into CD4+ CD8+ (double positive [DP]) thymocytes, and they generate such signals without apparent ligand engagements. Although ligand-independent signaling is unusual and might be unique to the pre-TCR, it is possible that other TCR complexes such as {alpha}ß TCR or {alpha}{gamma} TCR might also be able to signal the DN to DP transition in the absence of ligand engagement if they were expressed on DN thymocytes. Although {alpha}{gamma} TCR complexes efficiently signal DN thymocyte differentiation, it is not yet certain if {alpha}ß TCR complexes are also capable of signaling DN thymocyte differentiation, nor is it certain if such signaling is dependent upon ligand engagement. This study has addressed these questions by expressing defined {alpha}ß TCR transgenes in recombination activating gene 2–/– pre-T{alpha}–/– double deficient mice. In such double deficient mice, the only antigen receptors that can be expressed are those encoded by the {alpha}ß TCR transgenes. In this way, this study definitively demonstrates that {alpha}ß TCR can in fact signal the DN to DP transition. In addition, this study demonstrates that transgenic {alpha}ß TCRs signal the DN to DP transition even in the absence of their specific MHC–peptide ligands.

Key Words: DN to DP transition • {alpha}ß TCR transgene • ligand-independent signaling • pre-TCR/{alpha}{gamma} TCR



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 has been cited by other articles:



  Home | Help | Feedback | Subscriptions | Archive | Search
TABLE OF CONTENTS