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Autoantigen-specific interactions with CD4+ thymocytes control mature medullary thymic epithelial cell cellularity
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 1195344
Author(s) Irla, Magali; Hugues, Stéphanie; Gill, Jason; Nitta, Takeshi; Hikosaka, Yu; Williams, Ifor R; Hubert, François-Xavier; Scott, Hamish S; Takahama, Yousuke; Holländer, Georg A; Reith, Walter
Author(s) at UniBasel Holländer, Georg
Year 2008
Title Autoantigen-specific interactions with CD4+ thymocytes control mature medullary thymic epithelial cell cellularity
Journal Immunity
Volume 29
Number 3
Pages / Article-Number 451-63
Abstract Medullary thymic epithelial cells (mTECs) are specialized for inducing central immunological tolerance to self-antigens. To accomplish this, mTECs must adopt a mature phenotype characterized by expression of the autoimmune regulator Aire, which activates the transcription of numerous genes encoding tissue-restricted self-antigens. The mechanisms that control mature Aire(+) mTEC development in the postnatal thymus remain poorly understood. We demonstrate here that, although either CD4(+) or CD8(+) thymocytes are sufficient to sustain formation of a well-defined medulla, expansion of the mature mTEC population requires autoantigen-specific interactions between positively selected CD4(+) thymocytes bearing autoreactive T cell receptor (TCR) and mTECs displaying cognate self-peptide-MHC class II complexes. These interactions also involve the engagement of CD40 on mTECs by CD40L induced on the positively selected CD4(+) thymocytes. This antigen-specific TCR-MHC class II-mediated crosstalk between CD4(+) thymocytes and mTECs defines a unique checkpoint in thymic stromal development that is pivotal for generating a mature mTEC population competent for ensuring central T cell tolerance.
Publisher Cell Press
ISSN/ISBN 1074-7613
edoc-URL http://edoc.unibas.ch/dok/A6005527
Full Text on edoc No
Digital Object Identifier DOI 10.1016/j.immuni.2008.08.007
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/18799151
ISI-Number WOS:000259708900015
Document type (ISI) Journal Article
 
   

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