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

机译:FcεRIRIγ转基因小鼠中CD4-CD8-FcγRII / III + T和自然杀伤细胞前体的延迟成熟

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摘要

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.
机译:FcεRIγ(γ)是一组相关蛋白(ζ家族二聚体)的成员,它们既是Fc受体又是T细胞抗原受体(TCR)的信号传导成分。胎儿胸腺个体发育过程中γ的表达分析表明,它在克隆型TCR-α和TCR-β基因重排开始之前在早期胸腺细胞中表达,但在大多数成年胸腺细胞中被下调。为了探索γ在胸腺细胞发育中的可能作用,我们生成了转基因小鼠,其中该蛋白在个体发育的所有阶段均过表达。 γ的过表达抑制T细胞以及自然杀伤(NK)细胞的成熟。发育影响与转基因剂量有关,并与胎儿CD4-CD8-FcRII / III +胸腺细胞明显延迟成熟有关,胸腺细胞被认为包括T和NK细胞的祖细胞。这些结果表明,ζ链和γ链在胸腺细胞发育中发挥独特的功能,并表明Fc受体在调节胸腺内早期祖细胞的分化中可能起重要作用。

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