McCann Fiona E, Vanherberghen Bruno, Eleme Konstantina, Carlin Leo M, Newsam Ray J, Goulding David, Davis Daniel M
Department of Biological Sciences, Imperial College, London, United Kingdom.
J Immunol. 2003 Mar 15;170(6):2862-70. doi: 10.4049/jimmunol.170.6.2862.
In this study, we report the organization of cytoskeletal and large transmembrane proteins at the inhibitory and activating NK cell immunological or immune synapse (IS). Filamentous actin accumulates at the activating, but not the inhibitory, NK cell IS. However, surprisingly, ezrin and the associated protein CD43 are excluded from the inhibitory, but not the activating, NK cell IS. This distribution of ezrin and CD43 at the inhibitory NK cell IS is similar to that previously seen at the activating T cell IS. CD45 is also excluded from the inhibitory, but not activating, NK cell IS. In addition, electron microscopy reveals wide and narrow domains across the synaptic cleft. Target cell HLA-C, located by immunogold labeling, clusters where the synaptic cleft spans the size of HLA-C bound to the inhibitory killer Ig-like receptor. These data are consistent with assembly of the NK cell IS involving a combination of cytoskeletal-driven mechanisms and thermodynamics favoring the organization of receptor/ligand pairs according to the size of their extracellular domains.
在本研究中,我们报道了细胞骨架蛋白和大型跨膜蛋白在抑制性和激活性自然杀伤(NK)细胞免疫突触(IS)处的组织情况。丝状肌动蛋白在激活性NK细胞免疫突触处积累,而在抑制性NK细胞免疫突触处不积累。然而,令人惊讶的是,埃兹蛋白和相关蛋白CD43被排除在抑制性NK细胞免疫突触之外,而在激活性NK细胞免疫突触处却存在。埃兹蛋白和CD43在抑制性NK细胞免疫突触处的这种分布与之前在激活性T细胞免疫突触处观察到的分布相似。CD45也被排除在抑制性NK细胞免疫突触之外,而在激活性NK细胞免疫突触处不存在。此外,电子显微镜显示突触间隙存在宽域和窄域。通过免疫金标记定位的靶细胞HLA - C聚集在突触间隙跨越与抑制性杀伤细胞免疫球蛋白样受体结合的HLA - C大小的区域。这些数据与NK细胞免疫突触的组装一致,其涉及细胞骨架驱动机制和热力学的组合,有利于根据细胞外结构域的大小来组织受体/配体对。