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C/EBPα、GATA2、转化生长因子-β信号传导及表观遗传机制对嗜碱性粒细胞特异性蛋白酶基因的转录调控

Transcriptional regulation of basophil-specific protease genes by C/EBPα, GATA2, TGF-β signaling, and epigenetic mechanisms.

作者信息

Tojima Ryotaro, Nagata Kazuki, Ito Naoto, Ishii Kenta, Arai Takahiro, Ito Tomoka, Kasakura Kazumi, Nishiyama Chiharu

机构信息

Department of Biological Science and Technology, Faculty of Advanced Engineering, Tokyo University of Science, Tokyo, Japan.

出版信息

FEBS Lett. 2025 Mar;599(5):777-786. doi: 10.1002/1873-3468.15069. Epub 2024 Dec 11.

Abstract

Basophils and mast cells (MCs) play an important role in immune responses against allergens and parasitic infection. To elucidate the mechanisms that determine the commitment between basophils and mast cell (MCs), transcription factors and epigenetic modifications regulating the gene expression of basophil-specific enzymes, Mcpt8 and Mcpt11, were analyzed using bone marrow-derived (BM) cells containing basophils and MCs. Knockdown (KD) and overexpression experiments revealed that the transcription factor C/EBPα positively regulated the gene expression of Mcpt8 and Prss34 (encoding Mcpt11). Cebpa, Mcpt8, and Prss34 mRNAs levels were upregulated by histone deacetylases and downregulated by DNA methyltransferases. Gata2 KD significantly reduced the mRNA levels of Mcpt8 and Prss34, while TGF-β treatment increased those of Mcpt8 and Prss34. These results show that basophil-specific protease genes were transactivated by C/EBPα, GATA2, and TGF-β signaling and modified with epigenetic regulation.

摘要

嗜碱性粒细胞和肥大细胞在针对过敏原和寄生虫感染的免疫反应中发挥重要作用。为了阐明决定嗜碱性粒细胞和肥大细胞分化的机制,我们使用含有嗜碱性粒细胞和肥大细胞的骨髓来源细胞,分析了调节嗜碱性粒细胞特异性酶Mcpt8和Mcpt11基因表达的转录因子和表观遗传修饰。敲低(KD)和过表达实验表明,转录因子C/EBPα正向调节Mcpt8和Prss34(编码Mcpt11)的基因表达。Cebpa、Mcpt8和Prss34的mRNA水平被组蛋白脱乙酰酶上调,被DNA甲基转移酶下调。Gata2敲低显著降低了Mcpt8和Prss34的mRNA水平,而TGF-β处理则增加了Mcpt8和Prss34的mRNA水平。这些结果表明,嗜碱性粒细胞特异性蛋白酶基因被C/EBPα、GATA2和TGF-β信号转导激活,并受到表观遗传调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c945/11891402/ecef7fd38cc0/FEB2-599-777-g005.jpg

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