Fitzgerald L A, Denny J B, Baumbach G A, Ketcham C M, Roberts R M
J Cell Sci. 1984 Apr;67:1-23. doi: 10.1242/jcs.67.1.1.
The influence of altered carbohydrate structure on the surface number, distribution and turnover of plasma membrane glycoproteins has been studied in Chinese hamster ovary (CHO) cells by comparing three lines that are resistant to the cytotoxic effects of wheat germ agglutinin (WGA) with parental CHO cells. The glycoproteins investigated were members of a group of high molecular weight acidic glycoproteins (HMWAG). On parental cells these represent the major surface components that become labelled by lactoperoxidase-catalysed iodination. They are the only plasma membrane glycoproteins that bind WGA. The mutant lines also possess iodinatable surface polypeptides of high molecular weight, but these were less acidic and electrophoretically less diffuse than those from parental cells. These polypeptides in general did not bind [125I]WGA when two-dimensional polyacrylamide gels were overlaid with iodinated lectin. Mutant cells treated with fluorescein-conjugated WGA showed low surface fluorescence. However, the nuclear envelope and a small region in the perinuclear zone fluoresced strongly. Together, these results confirm that the surface glycoproteins of mutant cells had altered carbohydrate structure. Mouse antiserum prepared against the HMWAG, however, bound equally effectively to the mutant lines as to the parental lines. Indirect immunofluorescence experiments showed that the HMWAG had a fairly uniform distribution over the surface, and that internalization induced by second antibody occurred at a similar rate and in a similar manner in all lines, including the mutants. Electron microscopic observations using immunoperoxidase procedures confirmed the similarities in glycoprotein distribution on mutant and parental cells. Two mouse monoclonal antibodies raised against the HMWAG also revealed no difference in the number or topography of surface glycoproteins. Finally, the half-lives of several HMWAG in a parental and a mutant line (15B) maintained on low-serum medium were compared by means of a 125I/131I double-label technique. Half-lives of HMWAG from the former averaged 12 h and from the latter 11 h. It is concluded that the lack of complex termini on oligosaccharides of this particular group of CHO plasma membrane glycoproteins has no effect on their number, distribution or turnover.
通过比较三种对麦胚凝集素(WGA)细胞毒性作用具有抗性的细胞系与亲本中国仓鼠卵巢(CHO)细胞,研究了碳水化合物结构改变对质膜糖蛋白表面数量、分布和周转的影响。所研究的糖蛋白是一组高分子量酸性糖蛋白(HMWAG)的成员。在亲本细胞上,这些代表了通过乳过氧化物酶催化碘化而被标记的主要表面成分。它们是唯一能结合WGA的质膜糖蛋白。突变细胞系也具有可碘化的高分子量表面多肽,但这些多肽的酸性比亲本细胞的多肽弱,并且在电泳上扩散性较小。当二维聚丙烯酰胺凝胶用碘化凝集素覆盖时,这些多肽一般不结合[125I]WGA。用荧光素偶联的WGA处理的突变细胞显示出低表面荧光。然而,核膜和核周区的一个小区域荧光强烈。这些结果共同证实突变细胞的表面糖蛋白具有改变的碳水化合物结构。然而,针对HMWAG制备的小鼠抗血清与突变细胞系结合的效果与与亲本细胞系结合的效果相同。间接免疫荧光实验表明,HMWAG在表面具有相当均匀分布,并且二抗诱导的内化在所有细胞系(包括突变体)中以相似的速率和方式发生。使用免疫过氧化物酶方法的电子显微镜观察证实了突变细胞和亲本细胞上糖蛋白分布的相似性。两种针对HMWAG产生的小鼠单克隆抗体也未显示表面糖蛋白数量或拓扑结构上的差异。最后,通过125I/131I双标记技术比较了在低血清培养基上培养的亲本细胞系和突变细胞系(15B)中几种HMWAG的半衰期。来自前者的HMWAG半衰期平均为12小时,来自后者的为11小时。得出的结论是,这组CHO质膜糖蛋白的寡糖缺乏复杂末端对其数量、分布或周转没有影响。