T-cell receptor ligation by peptide/MHC induces activation of a caspase in immature thymocytes: the molecular basis of negative selection

T‐cell receptors (TCRs) are created by a stochastic gene rearrangement process during thymocyte development, generating thymocytes bearing useful, as well as unwanted, specificities. Within the latter group, autoreactive thymocytes arise which are subsequently eliminated via a thymocyte‐specific apo...

Full description

Saved in:
Bibliographic Details
Published in:The EMBO Journal Vol. 16; no. 9; pp. 2282 - 2293
Main Authors: Clayton, Linda K., Ghendler, Yoseph, Mizoguchi, Emiko, Patch, Raymond J., Ocain, Timothy D., Orth, Kim, Bhan, Atul K., Dixit, Vishva M., Reinherz, Ellis L.
Format: Journal Article
Language:English
Published: Chichester, UK John Wiley & Sons, Ltd 01-05-1997
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:T‐cell receptors (TCRs) are created by a stochastic gene rearrangement process during thymocyte development, generating thymocytes bearing useful, as well as unwanted, specificities. Within the latter group, autoreactive thymocytes arise which are subsequently eliminated via a thymocyte‐specific apoptotic mechanism, termed negative selection. The molecular basis of this deletion is unknown. Here, we show that TCR triggering by peptide/MHC ligands activates a caspase in double‐positive (DP) CD4+CD8+ thymocytes, resulting in their death. Inhibition of this enzymatic activity prevents antigen‐induced death of DP thymocytes in fetal thymic organ culture (FTOC) from TCR transgenic mice as well as apoptosis induced by anti‐CD3ϵ monoclonal antibody and corticosteroids in FTOC of normal C57BL/6 mice. Hence, a common caspase mediates immature thymocyte susceptibility to cell death.
Bibliography:istex:0472B96EA0AF33D49A95E9FD55BB07A5571DA47F
ark:/67375/WNG-LV62VN6R-G
ArticleID:EMBJ7590216
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ObjectType-Article-1
ObjectType-Feature-2
ISSN:0261-4189
1460-2075
DOI:10.1093/emboj/16.9.2282