Notch1 Regulates Maturation of CD4 super(+) and CD8 super(+) Thymocytes by Modulating TCR Signal Strength

Notch signaling regulates cell fate decisions in multiple lineages. We demonstrate in this report that retroviral expression of activated Notch1 in mouse thymocytes abrogates differentiation of immature CD4 super(+)CD8 super(+) thymocytes into both CD4 and CD8 mature single-positive T cells. The abi...

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Veröffentlicht in:Immunity (Cambridge, Mass.) Mass.), 2001-03, Vol.14 (3), p.253-264
Hauptverfasser: Izon, D J, Punt, JA, Xu, L, Karnell, F G, Allman, D, Myung, P S, Boerth, N J, Pui, J C, Koretzky, G A, Pear, W S
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Sprache:eng
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Zusammenfassung:Notch signaling regulates cell fate decisions in multiple lineages. We demonstrate in this report that retroviral expression of activated Notch1 in mouse thymocytes abrogates differentiation of immature CD4 super(+)CD8 super(+) thymocytes into both CD4 and CD8 mature single-positive T cells. The ability of Notch1 to inhibit T cell development was observed in vitro and in vivo with both normal and TCR transgenic thymocytes. Notch1-mediated developmental arrest was dose dependent and was associated with impaired thymocyte responses to TCR stimulation. Notch1 also inhibited TCR-mediated signaling in Jurkat T cells. These data indicate that constitutively active Notch1 abrogates CD4 super(+) and CD8 super(+) maturation by interfering with TCR signal strength and provide an explanation for the physiological regulation of Notch expression during thymocyte development.
ISSN:1074-7613