Williams G S, Malin M, Vremec D, Chang C H, Boyd R, Benoist C, Mathis D
Institut de Génétique et de Biologie Moléculaire et Cellulaire (CNRS/INSERM/ULP), Strasbourg, France.
Int Immunol. 1998 Dec;10(12):1957-67. doi: 10.1093/intimm/10.12.1957.
We have generated a second line of mice lacking a transcription factor thought to be a critical regulator of MHC class II gene expression, CIITA (for class II transactivator). Our and the previously published lines differ in the deletion that was engineered and by the fact that we removed the neomycin-resistance promoter and structural gene via the cre-loxP recombination system. Characterization of our line led to two new findings. First, a substantial number of cells can express class II molecules in the absence of CIITA, albeit at 5-fold reduced levels, most notably dendritic cells in s.c. lymph nodes; therefore, the CIITA gene cannot be an absolute 'master gene' controlling the expression of class II molecules, as had been thought. Second, in contrast to recent results on human cell lines, CIITA is not critically involved in the IFN-gamma-induced up-regulation of MHC class I genes.
我们培育出了第二代缺乏一种转录因子的小鼠品系,该转录因子被认为是MHC II类基因表达的关键调节因子,即II类反式激活因子(CIITA)。我们培育的品系与之前发表的品系在构建的缺失情况以及我们通过cre-loxP重组系统去除新霉素抗性启动子和结构基因这一事实上存在差异。对我们培育的品系进行表征得出了两个新发现。第一,大量细胞在没有CIITA的情况下能够表达II类分子,尽管表达水平降低了5倍,最显著的是皮下淋巴结中的树突状细胞;因此,CIITA基因不可能像之前认为的那样是控制II类分子表达的绝对“主基因”。第二,与最近关于人类细胞系的研究结果相反,CIITA在IFN-γ诱导的MHC I类基因上调过程中并非关键因素。