Zhang Xinxing, Sun Zhichao, Guo Suyu, Zhang Jiahui, Gu Wenjing, Chen Zhengrong, Huang Li
Department of Pediatric Pulmonology, Children's Hospital of Soochow University, Suzhou, Jiangsu, 215003, People's Republic of China.
J Asthma Allergy. 2021 Aug 5;14:955-966. doi: 10.2147/JAA.S318104. eCollection 2021.
It was demonstrated that membrane-associated RING-CH 1 (March 1) might play an important role in the pathogenesis of asthma.
The levels of mRNA and protein were measured by qRT-PCR and Western blot, respectively. Immunofluorescence assay was used to determine whether March1 co-locates with HDAC11. Co-immunoprecipitation was performed to examine the combination of proteins. Moreover, luciferase assay was used to measure the promoter activity of genes.
The mRNA and protein levels of both March1 and OX40 ligand (OX40L) were increased in the dendritic cells (DCs) from asthmatic children and asthmatic animals. Histone deacetylase 11 (HDAC11) protein was decreased in the DCs from asthmatic children and asthmatic model. Increasing of March1 or decreasing of March1 only affect the expression of HDAC11 in protein level. Besides, increasing of HDAC11 could inhibit OX40L expression, and decreasing of HDAC11 promoted OX40L expression in house dust mites (HDMs)-treated DCs. Increasing of HDAC11 notably reversed the promotion of March1 to OX40L expression. Our data further proved that March1 reduced the protein level of HDAC11 through inducing ubiquitination and degradation. HDAC11 combined with krüppel-like factor 4 (KLF4) to decrease the activity of OX40L gene promoter, thus to downregulate the level of OX40L.
Overall, our data showed that HDAC11 promoted KLF4-dependent OX40L decreasing. However, March1 promoted OX40L expression through enhancing the ubiquitination and degradation of HDAC11 and subsequent blocking the inhibition of HDAC11 to OX40L.
有研究表明,膜相关的RING-CH 1(March 1)可能在哮喘发病机制中起重要作用。
分别采用qRT-PCR和蛋白质免疫印迹法检测mRNA和蛋白质水平。免疫荧光分析用于确定March1是否与HDAC11共定位。进行免疫共沉淀以检测蛋白质的结合情况。此外,荧光素酶报告基因检测用于测量基因的启动子活性。
哮喘儿童和哮喘动物的树突状细胞(DCs)中March1和OX40配体(OX40L)的mRNA和蛋白质水平均升高。哮喘儿童和哮喘模型的DCs中组蛋白去乙酰化酶11(HDAC11)蛋白水平降低。March1的增加或减少仅在蛋白质水平上影响HDAC11的表达。此外,HDAC11的增加可抑制OX40L的表达,而HDAC11的减少则促进屋尘螨(HDMs)处理的DCs中OX40L的表达。HDAC11的增加显著逆转了March1对OX40L表达的促进作用。我们的数据进一步证明,March1通过诱导泛素化和降解降低HDAC11的蛋白质水平。HDAC11与Krüppel样因子4(KLF4)结合以降低OX40L基因启动子的活性,从而下调OX40L的水平。
总体而言,我们的数据表明HDAC11促进了KLF4依赖的OX40L减少。然而,March1通过增强HDAC11的泛素化和降解以及随后阻断HDAC11对OX40L的抑制作用来促进OX40L的表达。