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转录因子 GATA-1 对树突状细胞中细胞类型特异性基因表达的抑制作用。

Suppressive effects of transcription factor GATA-1 on cell type-specific gene expression in dendritic cells.

机构信息

Atopy (Allergy) Research Center, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan.

出版信息

Immunogenetics. 2010 Jul;62(7):421-9. doi: 10.1007/s00251-010-0444-1. Epub 2010 Apr 20.

Abstract

To evaluate the effects of the transcription factor GATA-1 on determining cell fate between dendritic cell (DC) and mast cell (MC) lineages, GATA-1 was exogenously expressed in bone marrow-derived (BM) DCs. Exogenous expression of GATA-1 by a retrovirus in BMDCs inhibited expression of CD11c, CD80, CD86, and major histocompatibility complex class II with suppression of antigen-presenting ability and morphological changes toward granulocyte-like cells. Transcription of MC proteases and c-kit was markedly upregulated by GATA-1. Expression of IRF-4 and -8 was markedly suppressed, whereas PU.1 mRNA level was not affected by GATA-1. Chromatin immunoprecipitation assay showed that recruitment of PU.1 on the IRF-8 promoter was reduced in GATA-1-expressing DCs. These results indicate that GATA-1 suppresses PU.1 function but not PU.1 transcription. Thus, GATA-1 appears to determine cell fate by regulating several cell-specific transcription factors.

摘要

为了评估转录因子 GATA-1 对树突状细胞 (DC) 和肥大细胞 (MC) 谱系之间细胞命运的决定作用,我们在外源性表达 GATA-1 的骨髓来源的 (BM) DCs 中进行了研究。通过逆转录病毒在 BMDC 中过表达 GATA-1,抑制了 CD11c、CD80、CD86 和主要组织相容性复合体 II 的表达,同时抑制了抗原呈递能力和向粒细胞样细胞的形态变化。GATA-1 显著上调了 MC 蛋白酶和 c-kit 的转录。IRF-4 和 -8 的表达明显受到抑制,而 GATA-1 对 PU.1 mRNA 水平没有影响。染色质免疫沉淀分析表明,在表达 GATA-1 的 DCs 中,PU.1 对 IRF-8 启动子的募集减少。这些结果表明,GATA-1 抑制了 PU.1 的功能而不是 PU.1 的转录。因此,GATA-1 似乎通过调节几个细胞特异性转录因子来决定细胞命运。

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