Valés-Gómez M, Reyburn H T, Mandelboim M, Strominger J L
Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
Immunity. 1998 Sep;9(3):337-44. doi: 10.1016/s1074-7613(00)80616-0.
The recognition of HLA-C molecules by specific inhibitory receptors is a crucial step in the regulation of natural killer (NK) cell function. Using soluble, recombinant HLA-C molecules and NK inhibitory receptors (NKIR, members of the immunoglobulin superfamily), we show that HLA-C binds to NKIR molecules with extremely fast association and dissociation rates, among the fastest of the immune system interactions so far studied. These kinetics may be essential for the biological function of NK cells, i.e., to facilitate the rapid immunosurveillance of cells for absent or diminished expression of class I MHC proteins.
特定抑制性受体对HLA - C分子的识别是自然杀伤(NK)细胞功能调节中的关键步骤。利用可溶性重组HLA - C分子和NK抑制性受体(NKIR,免疫球蛋白超家族成员),我们发现HLA - C与NKIR分子结合和解离的速率极快,是迄今为止研究的免疫系统相互作用中最快的之一。这些动力学特性可能对NK细胞的生物学功能至关重要,即有助于对I类MHC蛋白表达缺失或减少的细胞进行快速免疫监视。