胸腺细胞
T细胞受体
生物
CD8型
细胞生物学
Jurkat细胞
转基因
T细胞
双重否定
信号转导
细胞分化
免疫学
抗原
免疫系统
遗传学
基因
作者
David J. Izon,Jennifer A. Punt,Lanwei Xu,Fredrick G. Karnell,David Allman,Peggy Myung,Nancy J. Boerth,John C. Pui,Gary A. Koretzky,Warren S. Pear
出处
期刊:Immunity
[Cell Press]
日期:2001-03-01
卷期号:14 (3): 253-264
被引量:184
标识
DOI:10.1016/s1074-7613(01)00107-8
摘要
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+CD8+ 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+ and CD8+ maturation by interfering with TCR signal strength and provide an explanation for the physiological regulation of Notch expression during thymocyte development.
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