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诱导性共刺激分子对Th2细胞分化的转录调控

Transcriptional regulation of th2 differentiation by inducible costimulator.

作者信息

Nurieva Roza I, Duong Julie, Kishikawa Hiroko, Dianzani Umberto, Rojo Jose M, Ho I cheng, Flavell Richard A, Dong Chen

机构信息

Department of Immunology, University of Washington School of Medicine, Seattle, WA 98195, USA.

出版信息

Immunity. 2003 Jun;18(6):801-11. doi: 10.1016/s1074-7613(03)00144-4.

Abstract

Helper T (Th) cell differentiation is accompanied by complex transcriptional changes. Although costimulatory receptors are important in Th differentiation, the underlying mechanisms are poorly understood. Here we examine the transcriptional mechanisms by which ICOS regulates Th2 differentiation and selective IL-4 expression by effector T cells. We found impaired expression of c-Maf transcription factor functionally associated with the IL-4 defect in ICOS(-/-) cells. c-Maf expression in effector cells was regulated by IL-4 levels during Th differentiation. ICOS costimulation potentiated the T cell receptor (TcR)-mediated initial IL-4 production, possibly through the enhancement of NFATc1 expression. These data indicate that ICOS, by enhancing TcR signals at an early stage of T cell activation, regulates IL-4 transcription and T cell function in effector cells.

摘要

辅助性T(Th)细胞分化伴随着复杂的转录变化。尽管共刺激受体在Th细胞分化中很重要,但其潜在机制仍知之甚少。在这里,我们研究了ICOS调节Th2分化以及效应T细胞选择性表达IL-4的转录机制。我们发现,在ICOS基因敲除(-/-)细胞中,与IL-4缺陷功能相关的c-Maf转录因子表达受损。在Th细胞分化过程中,效应细胞中的c-Maf表达受IL-4水平调控。ICOS共刺激增强了T细胞受体(TcR)介导的初始IL-4产生,可能是通过增强NFATc1的表达来实现的。这些数据表明,ICOS通过在T细胞激活早期增强TcR信号,调节效应细胞中IL-4的转录和T细胞功能。

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