Huang Wufeng, Yu Changhui, Wu Hong, Liang Shixiu, Kang Jing, Zhou Zili, Liu Aihua, Liu Laiyu
Department of Respiratory and Critical Care Medicine, Nanfang Hospital, Southern Medical University, Guangzhou 510515, Guangdong Province, China; People's Hospital of Huazhou City. Huazhou 525100, Guangdong Province, China.
Department of Respiratory and Critical Care Medicine, Nanfang Hospital, Southern Medical University, Guangzhou 510515, Guangdong Province, China.
Biochim Biophys Acta Mol Cell Res. 2023 Oct;1870(7):119524. doi: 10.1016/j.bbamcr.2023.119524. Epub 2023 Jun 20.
The potential role of polycomb chromobox 4 (Cbx4), as a small ubiquitin-like ligase (SUMO) E3 ligase, in the development and exacerbation of asthma remains unclear. Hypoxia inducible factor-1 (HIF-1) is a key transcription factor in the cellular response to hypoxia and contributes to the pathogenesis and progression of a range of diseases, including asthma. Here, we aimed to investigate the interaction of Cbx4 with Hypoxia inducible factor-1α (HIF-1α) and the potent mechanism of action in asthma progression. In present study, in vitro and ex vivo results demonstrated that Cbx4 interacts with HIF-1α protein through its SUMO E3 ligase activity and enhances the sumoylation, which increases HIF-1 transactivation through Cbx4 and promotes the differentiation of Th9 cells, then in turn promotes the process of asthma. Treatment of inhibitors targeting SUMO E3 ligase activity of Cbx4 or HIF-1α can effectively reduce HIF-1α activation and differentiation of Th9 cells, which further attenuates the asthma in mouse model. Current results collectively demonstrated Cbx4 can govern HIF-1α to involve in Th9 cell differentiation promoting asthma by its SUMO E3 ligase activity, providing a new direction for clinical treatment of asthma.
作为一种小泛素样连接酶(SUMO)E3连接酶,多梳蛋白染色体框4(Cbx4)在哮喘的发生发展和病情加重中所起的潜在作用尚不清楚。缺氧诱导因子-1(HIF-1)是细胞对缺氧反应中的关键转录因子,在包括哮喘在内的一系列疾病的发病机制和进展中发挥作用。在此,我们旨在研究Cbx4与缺氧诱导因子-1α(HIF-1α)的相互作用以及在哮喘进展中的有效作用机制。在本研究中,体外和离体实验结果表明,Cbx4通过其SUMO E3连接酶活性与HIF-1α蛋白相互作用并增强其SUMO化,这通过Cbx4增加HIF-1的反式激活并促进Th9细胞的分化,进而促进哮喘进程。使用针对Cbx4或HIF-1α的SUMO E3连接酶活性的抑制剂进行治疗,可有效降低HIF-1α的激活和Th9细胞的分化,从而进一步减轻小鼠模型中的哮喘症状。目前的结果共同表明,Cbx4可通过其SUMO E3连接酶活性调控HIF-1α参与Th9细胞分化以促进哮喘,为哮喘的临床治疗提供了新方向。