| Literature DB >> 11290335 |
D J Izon1, J A Punt, L Xu, F G Karnell, D Allman, P S Myung, N J Boerth, J C Pui, G A Koretzky, W S Pear.
Abstract
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.Entities:
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Year: 2001 PMID: 11290335 DOI: 10.1016/s1074-7613(01)00107-8
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745