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携带TCR-β突变基因的转基因小鼠中的T细胞耗竭。

T cell depletion in transgenic mice carrying a mutant gene for TCR-beta.

作者信息

Krimpenfort P, Ossendorp F, Borst J, Melief C, Berns A

机构信息

Division of Molecular Genetics, The Netherlands Cancer Institute, Amsterdam.

出版信息

Nature. 1989 Oct 26;341(6244):742-6. doi: 10.1038/341742a0.

Abstract

Classical T lymphocytes recognize foreign antigens in the context of self major histocompatibility complex (MHC) molecules by means of the T-cell receptor (TCR)alpha beta heterodimer. The genes for TCR beta-chains, like immunoglobulin genes, are subject to allelic exclusion. The introduction of a functional TCR-beta gene into the germline of mice prevents rearrangement of endogenous TCR-beta genes. Here we report that the introduction of a non-functional TCR-beta genes. Here we report that the introduction of a non-functional TCR-beta gene with a deletion of the major part of the variable region (delta V-TCR-beta), also inhibits endogenous TCR-beta gene rearrangement. This inhibition is mediated via the encoded protein because impairment of endogenous TCR-beta gene rearrangement is not found if a frameshift mutation is introduced into the DJ region of the delta V-TCR-beta transgene. The delta V-TCR-beta transgene can lead to two phenotypes, in which lymphoid development is perturbed. Phenotype A is characterized by a severe impairment of both T and B cell development as reflected by the complete absence of certain lymphoid organs. In phenotype B, lymphoid organs are macroscopically normal, but T cell differentiation is impeded. Virtually all thymocytes lack membrane expression of TCR-alpha beta, but nevertheless carry the CD4 and CD8 antigens (CD4+CD8+ phenotype); they do not, however, mature further. The defect in mice of phenotype B but not of phenotype A can be corrected by the introduction of a functional TCR-beta gene.

摘要

经典T淋巴细胞通过T细胞受体(TCR)αβ异二聚体在自身主要组织相容性复合体(MHC)分子的背景下识别外来抗原。与免疫球蛋白基因一样,TCRβ链的基因也会发生等位基因排斥。将功能性TCR-β基因导入小鼠种系可阻止内源性TCR-β基因的重排。在此我们报告,导入一个可变区大部分缺失的无功能TCR-β基因(δV-TCR-β),也会抑制内源性TCR-β基因重排。这种抑制是通过编码蛋白介导的,因为如果在δV-TCR-β转基因的DJ区域引入移码突变,就不会发现内源性TCR-β基因重排受到损害。δV-TCR-β转基因可导致两种表型,其中淋巴细胞发育受到干扰。表型A的特征是T细胞和B细胞发育均严重受损,表现为某些淋巴器官完全缺失。在表型B中,淋巴器官在宏观上是正常的,但T细胞分化受到阻碍。几乎所有胸腺细胞都缺乏TCR-αβ的膜表达,但仍携带CD4和CD8抗原(CD4+CD8+表型);然而,它们不会进一步成熟。表型B而非表型A的小鼠中的缺陷可通过导入功能性TCR-β基因来纠正。

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