| Literature DB >> 19747858 |
Sophia D Sarafova1, Francois Van Laethem, Stanley Adoro, Terry Guinter, Susan O Sharrow, Lionel Feigenbaum, Alfred Singer.
Abstract
The lineage fate of developing thymocytes is determined by the persistence or cessation of T cell receptor (TCR) signaling during positive selection, with persistent TCR signaling required for CD4 lineage choice. We show here that transcriptional upregulation of CD4 expression is essential for error-free lineage choice during major histocompatibility complex class II (MHC II)-specific positive selection and is critical for error-free lineage choice in TCR-transgenic mice whose thymocytes compete for the identical selecting ligand. CD4 upregulation occurred for endogenously encoded CD4 coreceptors, but CD4 transgenes were downregulated during positive selection, disrupting MHC II-specific TCR signaling and causing lineage errors regardless of the absolute number or signaling strength of transgenic CD4 proteins. Thus, the kinetics of CD4 coreceptor expression during MHC II-specific positive selection determines the integrity of CD4 lineage choice, revealing an elegant symmetry between coreceptor kinetics and lineage choice.Entities:
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Year: 2009 PMID: 19747858 PMCID: PMC2758695 DOI: 10.1016/j.immuni.2009.07.006
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745