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FcεRIγ转基因小鼠中CD4-CD8-FcγRII/III+T细胞和自然杀伤细胞前体的成熟延迟

Delayed maturation of CD4- CD8- Fc gamma RII/III+ T and natural killer cell precursors in Fc epsilon RI gamma transgenic mice.

作者信息

Flamand V, Shores E W, Tran T, Huang K, Lee E, Grinberg A, Kinet J P, Love P E

机构信息

Laboratory of Molecular Allergy & Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, Maryland 20852, USA.

出版信息

J Exp Med. 1996 Nov 1;184(5):1725-35. doi: 10.1084/jem.184.5.1725.

Abstract

Fc epsilon RI gamma (gamma) is a member of a group of related proteins (the zeta-family dimers) that function as signal-transducing components of both Fc receptors and the T cell antigen receptor (TCR). Analysis of gamma expression during fetal thymus ontogeny revealed that it is expressed in early thymocytes, before the initiation of clonotypic TCR-alpha and TCR-beta gene rearrangement but is down-regulated in most adult thymocytes. To explore a possible role for gamma in thymocyte development, we generated transgenic mice in which this protein was overexpressed at all stages of ontogeny. Overexpression of gamma inhibited the maturation of T cells as well as natural killer (NK) cells. The developmental effects were transgene dose related and correlated with markedly delayed maturation of fetal CD4-CD8- FcRII/III+ thymocytes, cells thought to include the progenitors of both T and NK cells. These results suggest that the zeta and gamma chains serve distinctive functions in thymocyte development and indicate that Fc receptor(s) may play an important role in regulating the differentiation of early progenitor cells within the thymus.

摘要

FcεRIγ(γ)是一组相关蛋白(ζ家族二聚体)的成员,这些蛋白作为Fc受体和T细胞抗原受体(TCR)的信号转导成分发挥作用。对胎儿胸腺发育过程中γ表达的分析表明,它在早期胸腺细胞中表达,早于克隆型TCR-α和TCR-β基因重排的起始,但在大多数成年胸腺细胞中表达下调。为了探究γ在胸腺细胞发育中的可能作用,我们构建了转基因小鼠,其中该蛋白在发育的各个阶段均过度表达。γ的过度表达抑制了T细胞以及自然杀伤(NK)细胞的成熟。发育效应与转基因剂量相关,并与胎儿CD4-CD8-FcRII/III+胸腺细胞(被认为包括T细胞和NK细胞的祖细胞)的成熟明显延迟相关。这些结果表明,ζ链和γ链在胸腺细胞发育中发挥着独特的功能,并表明Fc受体可能在调节胸腺内早期祖细胞的分化中起重要作用。

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