Uhrberg Markus
Institute for Transplantation Diagnostics and Cell Therapeutics, Heinrich Heine University Clinic of Düsseldorf, Moorenstrasse 5, D-40225 Düsseldorf, Germany.
Mol Immunol. 2005 Feb;42(4):471-5. doi: 10.1016/j.molimm.2004.07.029.
Human NK cells are equipped with arrays of inhibitory and stimulatory KIR receptors, many of them specific for HLA class I molecules on target cells. These NK receptors enable the recognition of virally infected as well as malignantly transformed target cells, which have downregulated the expression of single or multiple HLA class I products. KIR are expressed in clonally distributed ways leading to highly individualized but stable NK cell repertoires. Here, progress is reviewed toward understanding the molecular mechanisms that govern the unusual expression characteristics of KIR genes. Recent results suggest that DNA methylation plays a crucial role in shaping the KIR repertoire and underline the importance of epigenetic mechanisms as regulatory switches in the immune system.
人类自然杀伤(NK)细胞配备了一系列抑制性和刺激性杀伤细胞免疫球蛋白样受体(KIR),其中许多受体对靶细胞上的I类人类白细胞抗原(HLA)分子具有特异性。这些NK受体能够识别病毒感染以及恶性转化的靶细胞,这些靶细胞下调了单个或多个I类HLA产物的表达。KIR以克隆分布的方式表达,导致高度个体化但稳定的NK细胞库。在此,我们综述了在理解调控KIR基因异常表达特征的分子机制方面所取得的进展。最近的结果表明,DNA甲基化在塑造KIR库中起着关键作用,并强调了表观遗传机制作为免疫系统调节开关的重要性。