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GATA 和 Smad 转录因子对黏膜肥大细胞特异性蛋白酶基因的协同调控。

Cooperative Regulation of the Mucosal Mast Cell-Specific Protease Genes and by GATA and Smad Transcription Factors.

机构信息

Laboratory of Molecular and Cellular Immunology, Department of Biological Science and Technology, Faculty of Industrial Science and Technology, Tokyo University of Science, Katsushika-ku, Tokyo 125-8585, Japan; and.

Division of Cell Biology, La Jolla Institute for Immunology, La Jolla, CA 92037.

出版信息

J Immunol. 2020 Mar 15;204(6):1641-1649. doi: 10.4049/jimmunol.1900094. Epub 2020 Jan 31.

Abstract

Mouse mast cell proteases (mMCP)-1 and -2 are specifically expressed in mucosal mast cells (MCs). However, the transcriptional regulation mechanism of the and genes induced in mucosal MCs is largely unknown. In the current study, we found that TGF-β stimulation drastically induced upregulation of and mRNA in mouse bone marrow-derived MCs (BMMCs). TGF-β-induced expression of and was markedly suppressed by transfection with small interfering RNA targeting or and moderately reduced by small interfering RNA. We next examined the roles of the hematopoietic cell-specific transcription factors GATA1 and GATA2 in the expression of and and demonstrated that knockdown of GATA1 and GATA2 reduced the mRNA levels of and in BMMCs. The recruitment of GATA2 and acetylation of histone H4 of the highly conserved GATA-Smad motifs, which were localized in the distal regions of the and genes, were markedly increased by TGF-β stimulation, whereas the level of GATA2 binding to the proximal GATA motif was not affected by TGF-β. A reporter assay showed that TGF-β stimulation upregulated GATA2-mediated transactivation activity in a GATA-Smad motif-dependent manner. We also observed that GATA2 and Smad4 interacted in TGF-β-stimulated BMMCs via immunoprecipitation and Western blotting analysis. Taken together, these results demonstrate that TGF-β induced mMCP-1 and -2 expression by accelerating the recruitment of GATA2 to the proximal regions of the and genes in mucosal MCs.

摘要

鼠类肥大细胞蛋白酶(mMCP)-1 和 -2 特异性表达于黏膜肥大细胞(MCs)。然而,黏膜 MCs 中诱导的 和 基因的转录调控机制在很大程度上仍是未知的。在本研究中,我们发现 TGF-β 刺激可显著诱导鼠骨髓来源的肥大细胞(BMMCs)中 和 mRNA 的上调。针对 或 的小干扰 RNA 转染可显著抑制 TGF-β诱导的 和 表达,并适度降低 小干扰 RNA 的表达。接下来,我们研究了造血细胞特异性转录因子 GATA1 和 GATA2 在 和 表达中的作用,并证实敲低 GATA1 和 GATA2 可降低 BMMCs 中 和 的 mRNA 水平。募集的 GATA2 和组蛋白 H4 的乙酰化高度保守的 GATA-Smad 基序,其位于 和 基因的远端区域,由 TGF-β 刺激明显增加,而 GATA2 与近端 GATA 基序的结合水平不受 TGF-β 影响。报告基因分析表明,TGF-β 刺激以 GATA-Smad 基序依赖的方式上调 GATA2 介导的转录激活活性。我们还观察到 GATA2 和 Smad4 通过免疫沉淀和 Western blot 分析在 TGF-β 刺激的 BMMCs 中相互作用。总之,这些结果表明,TGF-β 通过加速 GATA2 募集到黏膜 MCs 中 和 基因的近端区域,诱导 mMCP-1 和 -2 的表达。

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