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CD3εδ5/δ5突变小鼠中自然杀伤细胞的正常发育与功能

Normal development and function of natural killer cells in CD3 epsilon delta 5/delta 5 mutant mice.

作者信息

Renard V, Ardouin L, Malissen M, Milon G, Lebastard M, Gillet A, Malissen B, Vivier E

机构信息

Centre d'Immunologie, Institut National de la Santé et de la Recherche Médicale-Centre National de la Recherche Scientifique de Marseille-Luminy, Faculté de Luminy, France.

出版信息

Proc Natl Acad Sci U S A. 1995 Aug 1;92(16):7545-9. doi: 10.1073/pnas.92.16.7545.

Abstract

The CD3 epsilon polypeptide contributes to the cell surface display as well as to the signal transduction properties of the T-cell antigen receptor complex. Intriguingly, the distribution of CD3 epsilon is not restricted to T cells, since activated mouse, human, and avian natural killer (NK) cells do express intracytoplasmic CD3 epsilon polypeptides. CD3 epsilon is also present in the cytoplasm of fetal thymic T/NK bipotential progenitor cells, suggesting that it constitutes a component of the NK differentiation program. We report here that the genetic disruption of CD3 epsilon exon 5 alters neither NK cell development nor in vitro and in vivo NK functions, although it profoundly blocked T-cell development. These results support the notion that CD3 epsilon is dispensable for mouse NK cell ontogeny and function and further suggest that the common NK/T-cell progenitor cell utilizes CD3 epsilon as a mandatory component only when differentiating toward the T-cell lineage.

摘要

CD3ε多肽有助于T细胞抗原受体复合物在细胞表面的展示以及信号转导特性。有趣的是,CD3ε的分布并不局限于T细胞,因为活化的小鼠、人类和禽类自然杀伤(NK)细胞确实表达胞质内CD3ε多肽。CD3ε也存在于胎儿胸腺T/NK双潜能祖细胞的细胞质中,这表明它是NK细胞分化程序的一个组成部分。我们在此报告,CD3ε外显子5的基因破坏既不改变NK细胞的发育,也不改变体外和体内的NK功能,尽管它严重阻碍了T细胞的发育。这些结果支持了CD3ε对小鼠NK细胞的个体发生和功能是可有可无的这一观点,并进一步表明,常见的NK/T细胞祖细胞仅在向T细胞谱系分化时才将CD3ε用作必需成分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c420/41376/1c1d402ad80e/pnas01494-0420-a.jpg

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