Eriksson M, Ryan J C, Nakamura M C, Sentman C L
Umeå Center for Molecular Pathogenesis, Umeå University, Umeå, Sweden.
Immunology. 1999 Jun;97(2):341-7. doi: 10.1046/j.1365-2567.1999.00800.x.
When T effector cells meet antigen-bearing target cells, there is a specific accumulation of T-cell receptors, co-receptors and structural proteins at the point of cell-cell contact. Ly49 inhibitory receptors bind to murine major histocompatibility complex (MHC) class I molecules and prevent natural killer-(NK) cell cytotoxicity. In this study we have tested whether inhibitory receptors accumulate at the point of cell-cell contact when NK cells encounter target cells bearing MHC class I ligands for those inhibitory receptors. We have used RNK-16 effector cells that express Ly49A receptors and have found that there was a specific accumulation of Ly49A receptors at the point of NK cell-target cell contact when the target cells expressed H-2Dd. We also observed that engagement of Ly49A on NK cells resulted in an altered redistribution of potential triggering receptors CD2 and NKR-P1. These data indicate that inhibitory receptors, like activating receptors, may specifically aggregate at the point of cell-cell contact which may be necessary for them to mediate their full inhibitory effect.
当效应T细胞遇到携带抗原的靶细胞时,在细胞 - 细胞接触点会有T细胞受体、共受体和结构蛋白的特异性聚集。Ly49抑制性受体与小鼠主要组织相容性复合体(MHC)I类分子结合,并阻止自然杀伤(NK)细胞的细胞毒性。在本研究中,我们测试了当NK细胞遇到携带针对这些抑制性受体的MHC I类配体的靶细胞时,抑制性受体是否会在细胞 - 细胞接触点聚集。我们使用了表达Ly49A受体的RNK - 16效应细胞,并且发现当靶细胞表达H - 2Dd时,Ly49A受体在NK细胞 - 靶细胞接触点有特异性聚集。我们还观察到NK细胞上Ly49A的结合导致潜在触发受体CD2和NKR - P1的重新分布发生改变。这些数据表明,抑制性受体与激活受体一样,可能在细胞 - 细胞接触点特异性聚集,这可能是它们介导其完全抑制作用所必需的。