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携带重排β链基因的转基因小鼠中γδT细胞受体的同型排斥

Isotypic exclusion of gamma delta T cell receptors in transgenic mice bearing a rearranged beta-chain gene.

作者信息

Fenton R G, Marrack P, Kappler J W, Kanagawa O, Seidman J G

机构信息

Department of Genetics, Harvard Medical School, Boston, MA 02115.

出版信息

Science. 1988 Aug 26;241(4869):1089-92. doi: 10.1126/science.2970670.

Abstract

The rearrangement of T cell antigen receptor beta- and gamma-chain gene segments was studied in transgenic mice that bear a functional beta-chain gene. Virtually all CD3-positive T cells derived from transgenic mice express beta chains containing the transgene-encoded V beta 8.2 variable region on their surfaces and do not express endogenous beta-chain variable regions. Expression of endogenous V beta genes is inhibited at the level of somatic recombination during thymic ontogeny. Furthermore, rearrangements of the TCR gamma-chain genes are also markedly inhibited in these transgenic animals. Hence expression of the TCR beta transgene has led to allelic exclusion of alpha beta receptors and isotypic exclusion of gamma delta T cell receptors.

摘要

在携带功能性β链基因的转基因小鼠中,研究了T细胞抗原受体β链和γ链基因片段的重排。实际上,源自转基因小鼠的所有CD3阳性T细胞在其表面表达含有转基因编码的Vβ8.2可变区的β链,并且不表达内源性β链可变区。内源性Vβ基因的表达在胸腺发育过程中的体细胞重组水平受到抑制。此外,在这些转基因动物中,TCRγ链基因的重排也受到明显抑制。因此,TCRβ转基因的表达导致了αβ受体的等位基因排斥和γδT细胞受体的同型排斥。

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