Vedrenne J, Assier E, Pereno R, Bouzinba-Segard H, Azzarone B, Jasmin C, Charron D, Krief P
INSERM U 396, Institut Biomédical des Cordeliers, Paris, France.
Oncogene. 1997 Mar 27;14(12):1453-61. doi: 10.1038/sj.onc.1200971.
The expression of major histocompatibility complex (MHC) class II antigens is constitutive in professional antigen presenting cells (APCs) but can also be induced by interferon-gamma (IFN-gamma) on the majority of the non professional APCs (e.g. fibroblasts). We have recently characterised a new factor called IK which is an efficient inhibitor of IFN-gamma induction of MHC class II antigens expression. Here, we demonstrate a novel role for IK in MHC class II expression since over-expression of this protein by stable transfection into human B cells led to a total disappearance of constitutive MHC class II mRNA expression. The class II transactivator (CIITA) is necessary for both constitutive and IFN-gamma induced MHC class II expressions. Examination of CIITA mRNA in IK stably transfected clones revealed a marked reduction of CIITA mRNA transcription. Taken together these results demonstrate that the IK protein plays a key role in the constitutive expression of MHC class II antigens and that inhibition induced by IK is upstream of CIITA in this regulatory pathway.
主要组织相容性复合体(MHC)II类抗原在专职抗原呈递细胞(APC)中组成性表达,但在大多数非专职APC(如成纤维细胞)中也可被γ干扰素(IFN-γ)诱导表达。我们最近鉴定了一种名为IK的新因子,它是IFN-γ诱导MHC II类抗原表达的有效抑制剂。在此,我们证明了IK在MHC II类表达中的新作用,因为通过稳定转染将该蛋白导入人B细胞后,组成性MHC II类mRNA表达完全消失。II类反式激活因子(CIITA)对于组成性和IFN-γ诱导的MHC II类表达都是必需的。对稳定转染IK的克隆中的CIITA mRNA进行检测,发现CIITA mRNA转录显著减少。综合这些结果表明,IK蛋白在MHC II类抗原的组成性表达中起关键作用,并且在该调节途径中,IK诱导的抑制作用位于CIITA的上游。