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Notch对T细胞命运的调控。

Regulation of T cell fate by Notch.

作者信息

Robey E

机构信息

Department of Molecular and Cell Biology, University of California, Berkeley 94720, USA.

出版信息

Annu Rev Immunol. 1999;17:283-95. doi: 10.1146/annurev.immunol.17.1.283.

Abstract

The transmembrane receptor Notch participates in diverse cell fate decisions throughout embryonic development. Notch receptors and their ligands are expressed in the mammalian thymus, raising the possibility that Notch could regulate T cell fate decisions. Expression of a constitutively activated form of Notch in developing thymocytes causes thymocytes normally destined for the CD4 lineage to adopt the CD8 lineage instead. This suggests that Notch activity normally acts to direct CD4+CD8+ precursors to the CD8 lineage. The choice between CD4 and CD8 T cell fates is also controlled by MHC recognition during positive selection, implying that recognition of class I or II MHC might regulate Notch signaling. Possible models for the regulation of Notch by MHC recognition during CD4 versus CD8 lineage determination are discussed.

摘要

跨膜受体Notch在整个胚胎发育过程中参与多种细胞命运的决定。Notch受体及其配体在哺乳动物胸腺中表达,这增加了Notch可能调节T细胞命运决定的可能性。在发育中的胸腺细胞中表达组成型激活形式的Notch会导致通常注定进入CD4谱系的胸腺细胞转而采用CD8谱系。这表明Notch活性通常作用于将CD4+CD8+前体细胞导向CD8谱系。CD4和CD8 T细胞命运之间的选择在阳性选择过程中也受到MHC识别的控制,这意味着对I类或II类MHC的识别可能调节Notch信号传导。本文讨论了在CD4与CD8谱系确定过程中MHC识别调节Notch的可能模型。

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