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Notch信号通路控制早期T细胞谱系祖细胞的产生和分化。

Notch signaling controls the generation and differentiation of early T lineage progenitors.

作者信息

Sambandam Arivazhagan, Maillard Ivan, Zediak Valerie P, Xu Lanwei, Gerstein Rachel M, Aster Jon C, Pear Warren S, Bhandoola Avinash

机构信息

Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.

出版信息

Nat Immunol. 2005 Jul;6(7):663-70. doi: 10.1038/ni1216. Epub 2005 Jun 12.

Abstract

Signaling by the transmembrane receptor Notch is critical for T lineage development, but progenitor subsets that first receive Notch signals have not been defined. Here we identify an immature subset of early T lineage progenitors (ETPs) in the thymus that expressed the tyrosine kinase receptor Flt3 and had preserved B lineage potential at low progenitor frequency. Notch signaling was active in ETPs and was required for generation of the ETP population. Additionally, Notch signals contributed to the subsequent differentiation of ETPs. In contrast, multipotent hematopoietic progenitors circulated in the blood even in the absence of Notch signaling, suggesting that critical Notch signals during early T lineage development are delivered early after thymic entry.

摘要

跨膜受体Notch发出的信号对于T细胞谱系发育至关重要,但首次接收Notch信号的祖细胞亚群尚未明确。在此,我们在胸腺中鉴定出一个早期T细胞谱系祖细胞(ETP)的未成熟亚群,其表达酪氨酸激酶受体Flt3,且在低祖细胞频率下保留了B细胞谱系潜能。Notch信号在ETP中具有活性,并且是ETP群体生成所必需的。此外,Notch信号有助于ETP的后续分化。相比之下,即使在没有Notch信号的情况下,多能造血祖细胞也会在血液中循环,这表明早期T细胞谱系发育过程中的关键Notch信号在胸腺进入后早期就已传递。

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