PTPN22 alters the development of regulatory T cells in the thymus

PTPN22 encodes a tyrosine phosphatase that inhibits Src-family kinases responsible for Ag receptor signaling in lymphocytes and is strongly linked with susceptibility to a number of autoimmune diseases. As strength of TCR signal is critical to the thymic selection of regulatory T cells (Tregs), we e...

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Veröffentlicht in:The Journal of immunology (1950) 2012-06, Vol.188 (11), p.5267-5275
Hauptverfasser: Maine, Christian J, Hamilton-Williams, Emma E, Cheung, Jocelyn, Stanford, Stephanie M, Bottini, Nunzio, Wicker, Linda S, Sherman, Linda A
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Sprache:eng
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Zusammenfassung:PTPN22 encodes a tyrosine phosphatase that inhibits Src-family kinases responsible for Ag receptor signaling in lymphocytes and is strongly linked with susceptibility to a number of autoimmune diseases. As strength of TCR signal is critical to the thymic selection of regulatory T cells (Tregs), we examined the effect of murine PTPN22 deficiency on Treg development and function. In the thymus, numbers of pre-Tregs and Tregs increased inversely with the level of PTPN22. This increase in Tregs persisted in the periphery and could play a key part in the reduced severity observed in the PTPN22-deficient mice of experimental autoimmune encephalomyelitis, a mouse model of multiple sclerosis. This could explain the lack of association of certain autoimmune conditions with PTPN22 risk alleles.
ISSN:0022-1767
1550-6606
DOI:10.4049/jimmunol.1200150