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组蛋白去甲基化酶KDM6B对胶质瘤细胞中OLIG2的表观遗传调控

The Epigenetic Regulation of OLIG2 by Histone Demethylase KDM6B in Glioma Cells.

作者信息

Sui Aixia, Han Biaogang, Ren Wenjun, He Weiliang, Gao Chao, Han Xiaohui, Liu Shifeng, Zhang Yan, Qi Xueling, Guo Xiaoqiang

机构信息

Department of Oncology, Hebei General Hospital, Shijiazhuang, 050051, Hebei, China.

College of Postgraduate, Hebei North University, Zhangjiakou, 075000, Hebei, China.

出版信息

J Mol Neurosci. 2022 May;72(5):939-946. doi: 10.1007/s12031-022-01976-1. Epub 2022 Feb 7.

Abstract

Gliomas are common tumors that occur in the brain, accounting for 80% of all malignant brain tumors. Oligodendrocyte transcription factor 2 (OLIG2) is a key transcription factor and strongly expressed in gliomas, which drives proliferation and invasion of glioma cells. Our previous studies have shown that histone lysine (K) demethylase 6B (KDM6B) promotes glioma development. The data also showed that OLIG2 content was positively correlated with KDM6B. Based on this, we proposed that KDM6B may play biological roles by regulating OLIG2 expression. Subsequently, many experiments were performed including specific inhibitor treatment, gene knockdown, and chromatin immunoprecipitation (ChIP) array. These results indicated that inhibition of KDM6B enzymatic activity with GSK-J4 reduces OLIG2 gene expression and protein content. The KDM6B knockdown experiment yielded similar results, that is, it reduces the mRNA and protein level of OLIG2 in glioma cells. ChIP assay showed that the promoter of OLIG2 can be bound by KDM6B, which catalyzes the demethylation of H3K27me3 and increases the expression of OLIG2. This study reveals a new regulatory mechanism of OLIG2 by KDM6B, which has important implications for the future development of drugs for gliomas and other neurological diseases.

摘要

神经胶质瘤是常见的脑部肿瘤,占所有恶性脑肿瘤的80%。少突胶质细胞转录因子2(OLIG2)是一种关键转录因子,在神经胶质瘤中强烈表达,可驱动胶质瘤细胞的增殖和侵袭。我们之前的研究表明,组蛋白赖氨酸(K)去甲基化酶6B(KDM6B)促进神经胶质瘤的发展。数据还显示,OLIG2含量与KDM6B呈正相关。基于此,我们推测KDM6B可能通过调节OLIG2表达发挥生物学作用。随后,我们进行了许多实验,包括特异性抑制剂处理、基因敲低和染色质免疫沉淀(ChIP)阵列分析。这些结果表明,用GSK-J4抑制KDM6B酶活性可降低OLIG2基因表达和蛋白含量。KDM6B敲低实验也得到了类似结果,即它降低了胶质瘤细胞中OLIG2的mRNA和蛋白水平。ChIP分析表明,OLIG2启动子可被KDM6B结合,KDM6B催化H3K27me3去甲基化并增加OLIG2的表达。本研究揭示了KDM6B对OLIG2的一种新调控机制,这对神经胶质瘤及其他神经疾病未来药物的开发具有重要意义。

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