Lacorazza H Daniel, Miyazaki Yasushi, Di Cristofano Antonio, Deblasio Anthony, Hedvat Cyrus, Zhang Jin, Cordon-Cardo Carlos, Mao Shifeng, Pandolfi Pier Paolo, Nimer Stephen D
Laboratory of Molecular Aspects of Hematopoiesis, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Immunity. 2002 Oct;17(4):437-49. doi: 10.1016/s1074-7613(02)00422-3.
We utilized gene targeting by homologous recombination to define the role that MEF, a transcriptional activating member of the ETS family of transcription factors, plays in lymphopoiesis. MEF-/- mice have a profound reduction in the number of NK-T and NK cells. Purified MEF-/- NK cells cannot lyse tumor cell targets and secrete only minimal amounts of IFNgamma. Perforin protein expression is severely impaired in MEF-deficient NK cells, likely accounting for the lack of tumor cell cytotoxicity. Promoter studies and chromatin immunoprecipitation analyses demonstrate that MEF and not ETS-1 directly regulates transcription of the perforin gene in NK cells. Our results uncover a specific role of MEF in the development and function of NK cells and in innate immunity.
我们利用同源重组基因靶向技术来确定ETS转录因子家族的转录激活成员MEF在淋巴细胞生成中所起的作用。MEF基因敲除小鼠的自然杀伤T细胞(NK-T)和自然杀伤细胞(NK)数量大幅减少。纯化的MEF基因敲除NK细胞无法裂解肿瘤细胞靶标,且仅分泌极少量的γ干扰素。穿孔素蛋白表达在MEF缺陷的NK细胞中严重受损,这可能是其缺乏肿瘤细胞细胞毒性的原因。启动子研究和染色质免疫沉淀分析表明,在NK细胞中,直接调节穿孔素基因转录的是MEF而非ETS-1。我们的研究结果揭示了MEF在NK细胞的发育、功能以及固有免疫中的特定作用。