Gorelik E, Jay G, Kim M, Hearing V J, DeLeo A, McCoy J P
Pittsburgh Cancer Institute, Pennsylvania 15213.
Cancer Res. 1991 Oct 1;51(19):5212-8.
An H-2Kb negative BL6 melanoma clone (BL6-8) was transfected with plasmids containing either the class I H-2Kb or class II H-2IAk gene in combination with the neor gene. The effects of the transfected genes on the expression of the melanoma-associated antigen (MAA) recognized by the monoclonal antibodies MM2-9B6 and MM2-3C6 and the cell surface carbohydrates recognized by 15 different lectins were studied. The original H-2Kb- clone or clones transfected with neor or class II H-2IAk genes expressed high levels of MAA and very low levels of soybean agglutinin (SBA), Griffonia simplicifolia I-B4 (GSIB4), and peanut agglutinin (PNA) lectin-binding sites. In contrast, clones that expressed high levels of the transfected H-2Kb gene completely lost the expression of MAA. In addition, these clones were characterized by the appearance of high levels of expression of the sugars specifically reacting with SBA, GSIB4, and PNA lectins. When the original BL6-8 clone was transfected with the H-2Kd gene, 25 clones subsequently isolated had relatively low expression of the transfected H-2Kd gene but high expression of the endogenous H-2Kb gene accompanied by an alteration in expression of the MAA and lectin binding identical with patterns common for H-2Kb+ melanoma cells. These changes were not due to the transfection, plasmid construction, or place of insertion, since similar phenotypic characteristics were found in H-2Kb+ but not H-2Kb- clones isolated from the N-methyl-N'-nitro-N-nitrosoguanidine-treated BL6T2 or parental BL6 melanoma lines. In total, 73 BL6 melanoma clones were investigated and all of the 41 H-2Kb+ clones displayed loss of MAA and appearance of SBA, GSIB4, and PNA-binding sugars. None of the 32 H-2Kb- clones showed these changes. This study indicates that the class I H-2Kb gene product might alter several phenotypic properties of BL6 melanoma cells. The mechanisms of these changes remain unknown. We consider that these effects of the class I H-2Kb gene are indirect, involving interactions with the B-tropic ecotropic retrovirus specific for melanomas of C57BL/6 mice origin.
将含有I类H-2Kb或II类H-2IAk基因并与新霉素抗性基因(neor)组合的质粒转染到一个H-2Kb阴性的BL6黑色素瘤克隆(BL6-8)中。研究了转染基因对单克隆抗体MM2-9B6和MM2-3C6所识别的黑色素瘤相关抗原(MAA)表达以及15种不同凝集素所识别的细胞表面碳水化合物表达的影响。原始的H-2Kb-克隆或转染了neor或II类H-2IAk基因的克隆表达高水平的MAA以及极低水平的大豆凝集素(SBA)、简氏刀豆凝集素I-B4(GSIB4)和花生凝集素(PNA)凝集素结合位点。相反,表达高水平转染H-2Kb基因的克隆完全丧失了MAA的表达。此外,这些克隆的特征是出现了与SBA、GSIB4和PNA凝集素特异性反应的糖的高水平表达。当用H-2Kd基因转染原始的BL6-8克隆时,随后分离出的25个克隆中,转染的H-2Kd基因表达相对较低,但内源性H-2Kb基因表达较高,同时伴随着MAA表达的改变以及凝集素结合模式的改变,这与H-2Kb+黑色素瘤细胞常见的模式相同。这些变化不是由于转染、质粒构建或插入位置引起的,因为从经N-甲基-N'-硝基-N-亚硝基胍处理的BL6T2或亲本BL6黑色素瘤系中分离出的H-2Kb+克隆而非H-2Kb-克隆中发现了类似的表型特征。总共研究了73个BL6黑色素瘤克隆,所有41个H-2Kb+克隆均表现出MAA丧失以及SBA、GSIB4和PNA结合糖的出现。32个H-2Kb-克隆均未显示出这些变化。这项研究表明,I类H-2Kb基因产物可能会改变BL6黑色素瘤细胞的几种表型特性。这些变化的机制仍然未知。我们认为I类H-2Kb基因的这些作用是间接的,涉及与源自C57BL/6小鼠黑色素瘤的B嗜性亲嗜性逆转录病毒的相互作用。