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Upregulation of CD4 Expression during MHC Class II-Specific Positive Selection Is Essential for Error-free Lineage Choice

  1. Author:
    Sarafova, S. D.
    Van Laethem, F.
    Adoro, S.
    Guinter, T.
    Sharrow, S. O.
    Feigenbaum, L.
    Singer, A.
  2. Author Address

    Sarafova, Sophia D.; Van Laethem, Francois, Adoro, Stanley, Guinter, Terry, Sharrow, Susan O.; Singer, Alfred] NCI, Expt Immunol Branch, Bethesda, MD 20892 USA. [Feigenbaum, Lionel] NCI, SAIC Frederick, Frederick Canc Res & Dev Ctr, Frederick, MD 21702 USA. [Sarafova, Sophia D.] Davidson Coll, Dept Biol, Davidson, NC 28036 USA.
    1. Year: 2009
  1. Journal: Immunity
    1. 31
    2. 3
    3. Pages: 480-490
  2. Type of Article: Article
  1. 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 MIHC II-specific positive selection determines the integrity of CD4 lineage choice, revealing an elegant symmetry between coreceptor kinetics and lineage choice.

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External Sources

  1. DOI: 10.1016/j.immuni.2009.07.006
  2. PMID: 19747858

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