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转录调节蛋白活化T细胞核因子家族在脂肪生成中的潜在作用。

A potential role for the nuclear factor of activated T cells family of transcriptional regulatory proteins in adipogenesis.

作者信息

Ho I C, Kim J H, Rooney J W, Spiegelman B M, Glimcher L H

机构信息

Department of Immunology and Infectious Diseases, Harvard School of Public Health, 651 Huntington Avenue, Boston, MA 02115, USA.

出版信息

Proc Natl Acad Sci U S A. 1998 Dec 22;95(26):15537-41. doi: 10.1073/pnas.95.26.15537.

Abstract

NFAT (nuclear factor of activated T cells) is a family of transcription factors implicated in the control of cytokine and early immune response gene expression. Recent studies have pointed to a role for NFAT proteins in gene regulation outside of the immune system. Herein we demonstrate that NFAT proteins are present in 3T3-L1 adipocytes and, upon fat cell differentiation, bind to and transactivate the promoter of the adipocyte-specific gene aP2. Further, fat cell differentiation is inhibited by cyclosporin A, a drug shown to prevent NFAT nuclear localization and hence function. Thus, these data suggest a role for NFAT transcription factors in the regulation of the aP2 gene and in the process of adipocyte differentiation.

摘要

活化T细胞核因子(NFAT)是一类转录因子家族,与细胞因子控制和早期免疫反应基因表达有关。最近的研究表明NFAT蛋白在免疫系统之外的基因调控中发挥作用。在此我们证明NFAT蛋白存在于3T3-L1脂肪细胞中,并且在脂肪细胞分化时,会结合并反式激活脂肪细胞特异性基因aP2的启动子。此外,环孢素A可抑制脂肪细胞分化,环孢素A是一种已证实可阻止NFAT入核定位并因此抑制其功能的药物。因此,这些数据表明NFAT转录因子在aP2基因调控及脂肪细胞分化过程中发挥作用。

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