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白细胞介素6诱导NFATc2表达促进2型辅助性T细胞分化。

Induction of NFATc2 expression by interleukin 6 promotes T helper type 2 differentiation.

作者信息

Diehl Sean, Chow Chi-Wing, Weiss Linda, Palmetshofer Alois, Twardzik Thomas, Rounds Laura, Serfling Edgar, Davis Roger J, Anguita Juan, Rincón Mercedes

机构信息

Immunobiology Program, Department of Medicine, Given Medical Building, University of Vermont, Burlington, VT 05405, USA.

出版信息

J Exp Med. 2002 Jul 1;196(1):39-49. doi: 10.1084/jem.20020026.

Abstract

Interleukin (IL)-6 is produced by professional antigen-presenting cells (APCs) such as B cells, macrophages, and dendritic cells. It has been previously shown that APC-derived IL-6 promotes the differentiation of naive CD4+ T cells into effector T helper type 2 (Th2) cells. Here, we have studied the molecular mechanism for IL-6-mediated Th2 differentiation. During the activation of CD4+ T cells, IL-6 induces the production of IL-4, which promotes the differentiation of these cells into effector Th2 cells. Regulation of IL-4 gene expression by IL-6 is mediated by nuclear factor of activated T cells (NFAT), as inhibition of NFAT prevents IL-6-driven IL-4 production and Th2 differentiation. IL-6 upregulates NFAT transcriptional activity by increasing the levels of NFATc2. The ability of IL-6 to promote Th2 differentiation is impaired in CD4+ T cells that lack NFATc2, demonstrating that NFATc2 is required for regulation of IL-4 gene expression by IL-6. Regulation of NFATc2 expression and NFAT transcriptional activity represents a novel pathway by which IL-6 can modulate gene expression.

摘要

白细胞介素(IL)-6由专业抗原呈递细胞(APC)产生,如B细胞、巨噬细胞和树突状细胞。先前已表明,APC来源的IL-6促进初始CD4+T细胞分化为效应性辅助性T细胞2型(Th2)细胞。在此,我们研究了IL-6介导的Th2分化的分子机制。在CD4+T细胞激活过程中,IL-6诱导IL-4的产生,IL-4促进这些细胞分化为效应性Th2细胞。IL-6对IL-4基因表达的调节由活化T细胞核因子(NFAT)介导,因为抑制NFAT可阻止IL-6驱动的IL-4产生和Th2分化。IL-6通过增加NFATc2的水平上调NFAT转录活性。在缺乏NFATc2的CD4+T细胞中,IL-6促进Th2分化的能力受损,这表明NFATc2是IL-6调节IL-4基因表达所必需的。NFATc2表达和NFAT转录活性的调节代表了IL-6调节基因表达的一条新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8504/2194007/b8d477a8c248/20020026f1.jpg

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