Zhou Haixia, Brekman Angelika, Zuo Wu-Lin, Ou Xuemei, Shaykhiev Renat, Agosto-Perez Francisco J, Wang Rui, Walters Matthew S, Salit Jacqueline, Strulovici-Barel Yael, Staudt Michelle R, Kaner Robert J, Mezey Jason G, Crystal Ronald G, Wang Guoqing
Department of Respiratory Medicine, West China Hospital, Sichuan University, Sichuan 610041, China; Department of Genetic Medicine, Weill Cornell Medical College, New York, NY 10065;
Department of Genetic Medicine, Weill Cornell Medical College, New York, NY 10065;
J Immunol. 2016 Apr 1;196(7):3159-67. doi: 10.4049/jimmunol.1502400. Epub 2016 Feb 29.
In the process of seeking novel lung host defense regulators by analyzing genome-wide RNA sequence data from normal human airway epithelium, we detected expression of POU domain class 2-associating factor 1 (POU2AF1), a known transcription cofactor previously thought to be expressed only in lymphocytes. Lymphocyte contamination of human airway epithelial samples obtained by bronchoscopy and brushing was excluded by immunohistochemistry staining, the observation of upregulation of POU2AF1 in purified airway basal stem/progenitor cells undergoing differentiation, and analysis of differentiating single basal cell clones. Lentivirus-mediated upregulation of POU2AF1 in airway basal cells induced upregulation of host defense genes, including MX1, IFIT3, IFITM, and known POU2AF1 downstream genes HLA-DRA, ID2, ID3, IL6, and BCL6. Interestingly, expression of these genes paralleled changes of POU2AF1 expression during airway epithelium differentiation in vitro, suggesting POU2AF1 helps to maintain a host defense tone even in pathogen-free condition. Cigarette smoke, a known risk factor for airway infection, suppressed POU2AF1 expression both in vivo in humans and in vitro in human airway epithelial cultures, accompanied by deregulation of POU2AF1 downstream genes. Finally, enhancing POU2AF1 expression in human airway epithelium attenuated the suppression of host defense genes by smoking. Together, these findings suggest a novel function of POU2AF1 as a potential regulator of host defense genes in the human airway epithelium.
在通过分析正常人呼吸道上皮细胞的全基因组RNA序列数据来寻找新型肺宿主防御调节因子的过程中,我们检测到POU结构域2相关因子1(POU2AF1)的表达,该转录辅因子此前被认为仅在淋巴细胞中表达。通过免疫组织化学染色、观察纯化的气道基底干细胞/祖细胞在分化过程中POU2AF1的上调情况以及对分化的单个基底细胞克隆进行分析,排除了支气管镜检查和刷检获得的人呼吸道上皮样本中的淋巴细胞污染。慢病毒介导的气道基底细胞中POU2AF1的上调诱导了宿主防御基因的上调,包括MX1、IFIT3、IFITM以及已知的POU2AF1下游基因HLA-DRA、ID2、ID3、IL6和BCL6。有趣的是,这些基因的表达与体外气道上皮分化过程中POU2AF1表达的变化平行,表明POU2AF1即使在无病原体的情况下也有助于维持宿主防御状态。香烟烟雾是已知的气道感染危险因素,在人体体内和人呼吸道上皮培养物体外均抑制POU2AF1的表达,并伴有POU2AF1下游基因的失调。最后,增强人呼吸道上皮中POU2AF1的表达可减轻吸烟对宿主防御基因的抑制作用。总之,这些发现表明POU2AF1在人呼吸道上皮中作为宿主防御基因潜在调节因子的新功能。