Gavioli R, Zhang Q J, Masucci M G
Microbiology and Tumor Biology Center, Karolinska Institute, Stockholm, Sweden.
Hum Immunol. 1996 Aug;49(1):1-12. doi: 10.1016/0198-8859(96)00031-6.
The capacity of MHC class I to protect target cells from NK is well established, but the mechanism by which these molecules influence NK recognition and the physical properties associated with this function remain poorly defined. We have examined this issue using as a model the HLA-A11 allele. HLA-A11 expression correlated with reduced susceptibility to NK and interferon-activated cytotoxicity in transfected sublines of the A11-defective Burkitt's lymphoma WW2-BL and the HLA class I A,B-null C1R cell line. Protection was also achieved by transfection of HLA-A11 in the peptide processing mutant T2 cells line (T2/A11), despite a very low expression of the transfected product at the cell surface. Induction of surface HLA-A11 by culture of T2/A11 cells at 26 degrees C or in the presence of beta 2m did not affect lysis, whereas NK sensitivity was restored by culture in the presence of HLA-All-binding synthetic peptides derived from viral or cellular proteins. Acid treatment rendered T2/A11 and C1R/A11 cells sensitive to lysis, but protection was restored after preincubation with peptide preparations derived from surface stripping of T2/A11 cells. Similar peptide preparations from T2 cells had no effect. The results suggest that NK protection is mediated by HLA-A11 molecules carrying a particular set of peptides that are translocated to the site of MHC class I assembly in the ER in a TAP-independent fashion.
MHC I类分子保护靶细胞免受自然杀伤细胞(NK)攻击的能力已得到充分证实,但这些分子影响NK识别的机制以及与该功能相关的物理特性仍不清楚。我们以HLA - A11等位基因为模型研究了这个问题。在有缺陷的A11伯基特淋巴瘤WW2 - BL转染亚系和HLA I类A、B缺失的C1R细胞系中,HLA - A11的表达与对NK和干扰素激活的细胞毒性的敏感性降低相关。尽管转染产物在细胞表面的表达非常低,但在肽加工突变体T2细胞系(T2/A11)中通过转染HLA - A11也实现了保护作用。在26℃培养T2/A11细胞或在存在β2微球蛋白(β2m)的情况下诱导表面HLA - A11,并不影响细胞裂解,而在存在源自病毒或细胞蛋白的与HLA - A11结合的合成肽的情况下培养可恢复NK敏感性。酸处理使T2/A11和C1R/A11细胞对裂解敏感,但在用源自T2/A11细胞表面剥离的肽制剂预孵育后保护作用得以恢复。来自T2细胞的类似肽制剂则没有效果。结果表明,NK保护作用是由携带一组特定肽段的HLA - A11分子介导的,这些肽段以不依赖抗原加工相关转运体(TAP)的方式转运到内质网中MHC I类分子组装位点。