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Ptprk和Themis的相邻基因缺失导致LEC大鼠出现T辅助免疫缺陷(thid)。

Contiguous gene deletion of Ptprk and Themis causes T-helper immunodeficiency (thid) in the LEC rat.

作者信息

Iwata Ryohei, Sasaki Nobuya, Agui Takashi

机构信息

Department of Disease Control, Hokkaido University, Sapporo, Japan.

出版信息

Biomed Res. 2010 Feb;31(1):83-7. doi: 10.2220/biomedres.31.83.

Abstract

The LEC rat has a spontaneous mutation of T-helper immunodeficiency (thid), which causes a marked defect in T cell maturation from double positive (DP) to CD4 single positive (SP) cells in the thymus. Previously, we identified the contiguous gene deletion of Ptprk and Themis genes in the thid locus that causes the simultaneous loss of expression of both genes, and the exogenous Ptprk expression partially rescued this phenotype. To determine whether the deletion of Themis influences thid phenotype, bone marrow (BM) cells were transduced with lentiviral vector expressing Themis gene, and were transplanted into X-ray-irradiated LEC rats. Interestingly, the exogenous Themis expression rescued the development of CD4 SP cells as well as Ptprk. The result suggests that the deficiency of both genes is responsible for the thid mutation, and that both genes are indispensable for the development of SP cells from DP cells in the thymus.

摘要

LEC大鼠存在T辅助免疫缺陷(thid)的自发突变,这导致胸腺中T细胞从双阳性(DP)向CD4单阳性(SP)细胞成熟过程出现明显缺陷。此前,我们在thid位点鉴定出Ptprk和Themis基因的连续基因缺失,这导致两个基因的表达同时丧失,并且外源性Ptprk表达部分挽救了这种表型。为了确定Themis的缺失是否影响thid表型,用表达Themis基因的慢病毒载体转导骨髓(BM)细胞,并将其移植到经X射线照射的LEC大鼠体内。有趣的是,外源性Themis表达挽救了CD4 SP细胞以及Ptprk的发育。结果表明,两个基因的缺陷是thid突变的原因,并且这两个基因对于胸腺中DP细胞发育为SP细胞都是不可或缺的。

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