Wang Z, Hu X Z, Tatake R J, Yang S Y, Zeff R A, Ferrone S
Department of Microbiology and Immunology, New York Medical College, Valhalla 10595.
Cancer Res. 1993 Sep 15;53(18):4303-9.
beta 2-Microglobulin (beta 2-mu) gene-null human melanoma FO-1 cells display lower reactivity with anti-HLA class I monoclonal antibodies (mAb) following transfection with a wild-type mouse beta 2-mu gene (referred to as FO-1C cells) than following transfection with a wild-type human beta 2-mu gene (referred to as FO-1H cells). Furthermore, binding assays with a panel of anti-HLA class I mAb detected higher reactivity of FO-1C cells with mAb TP25.99 than with mAb CR1-S63, CR10-215, CR11-115, TP67, and W6/32 but similar reactivity of FO-1H cells with all the mAb tested. While mAb TP25.99 recognizes a determinant expressed on beta 2-mu-free and beta 2-mu-associated HLA class I heavy chains, the remaining mAb recognize determinants expressed only on beta 2-mu-associated HLA class I heavy chains. The differential effects of mouse and human beta 2-mu on the reactivity with anti-HLA class I mAb of FO-1 cells reflect more than one mechanism. Besides abnormalities in the processing of HLA class I heavy chains associated with mouse beta 2-mu, this molecular complex appears to be unstable on the plasma membrane of FO-1 cells. To analyze the interaction of mouse beta 2-mu with HLA-A and -B antigens, the HLA phenotype of FO-1 cells was determined, using a combination of isoelectric focusing analysis of antigens immunoprecipitated from radiolabeled cells with mAb to monomorphic determinants of HLA class I antigens, binding assays with a limited number of mAb recognizing HLA class I allospecificities, and sequence-specific oligonucleotide probe typing. Although association with mouse beta 2-mu does not cause marked differences in the expression of HLA-A25 and -B8 antigens on the cell surface of FO-1 cells, it causes a selective reduction in the expression of determinants recognized by anti-HLA-A mAb F4/72 and VF19-LL67 and by anti-HLA class I mAb W6/32 on HLA-A25 allospecificities. The differential effect of the association with mouse beta 2-mu on the antigenic profile of HLA-A25 and -B8 antigens may reflect the different characteristics of the amino acids at residue 12, which interact with residue 33 of beta 2-mu. The latter residue is the only one to differ between human and mouse beta 2-mu in the stretch of amino acids interacting with the alpha 1 and alpha 2 domains of HLA class I heavy chains.(ABSTRACT TRUNCATED AT 400 WORDS)
β2-微球蛋白(β2-μ)基因缺失的人黑色素瘤FO-1细胞在用野生型小鼠β2-μ基因转染后(称为FO-1C细胞),与抗HLA I类单克隆抗体(mAb)的反应性低于用野生型人β2-μ基因转染后(称为FO-1H细胞)。此外,用一组抗HLA I类mAb进行的结合试验检测到,FO-1C细胞与mAb TP25.99的反应性高于与mAb CR1-S63、CR10-215、CR11-115、TP67和W6/32的反应性,但FO-1H细胞与所有测试的mAb的反应性相似。虽然mAb TP25.99识别在无β2-μ和与β2-μ相关的HLA I类重链上表达的决定簇,但其余mAb仅识别在与β2-μ相关的HLA I类重链上表达的决定簇。小鼠和人β2-μ对FO-1细胞与抗HLA I类mAb反应性的不同影响反映了不止一种机制。除了与小鼠β2-μ相关的HLA I类重链加工异常外,这种分子复合物在FO-1细胞的质膜上似乎不稳定。为了分析小鼠β2-μ与HLA-A和-B抗原的相互作用,使用从放射性标记细胞中免疫沉淀的抗原的等电聚焦分析与识别HLA I类抗原单态决定簇的mAb、用有限数量识别HLA I类同种特异性的mAb进行的结合试验以及序列特异性寡核苷酸探针分型相结合的方法,确定了FO-1细胞的HLA表型。虽然与小鼠β2-μ的结合不会导致FO-1细胞表面HLA-A25和-B8抗原表达的明显差异,但它会导致抗HLA-A mAb F4/72和VF19-LL67以及抗HLA I类mAb W6/32识别的决定簇在HLA-A25同种特异性上的表达选择性降低。与小鼠β2-μ结合对HLA-A25和-B8抗原抗原谱的不同影响可能反映了第12位氨基酸的不同特征,该氨基酸与β2-μ的第33位残基相互作用。后一个残基是在与HLA I类重链的α1和α2结构域相互作用的氨基酸序列中人与小鼠β2-μ之间唯一不同的残基。(摘要截断于400字)