Drusková E, Bízik J, Grófová M
Department of Physiology, School of Medicine, Comenius University, Bratislava, Slovakia.
Neoplasma. 1994;41(1):3-7.
Using immunological techniques, the synthesis of alpha 2-macroglobulin was studied in established cell lines derived from human glioblastomas multiforme. alpha 2-Macroglobulin was detected in cytoplasm and in the culture medium of the analyzed cell lines. Radioimmunoprecipitation revealed a protein with M(r) corresponding to alpha 2-macroglobulin in the medium conditioned by U-118MG and U-343MG cells. On the other hand, using immunoblot analysis, alpha 2-macroglobulin was detected in all of the analyzed lines. In immunofluorescence test, alpha 2-macroglobulin was determined also in all four cell lines, but with different staining pattern. Conditioned culture medium (CCM) of U-536MG cells with the lowest level of alpha 2-macroglobulin exerted the lowest mitogenic activity for human fibroblasts.
利用免疫学技术,在源自多形性胶质母细胞瘤的已建细胞系中研究了α2-巨球蛋白的合成。在分析的细胞系的细胞质和培养基中检测到了α2-巨球蛋白。放射免疫沉淀显示,由U-118MG和U-343MG细胞条件培养基中的一种蛋白,其分子量与α2-巨球蛋白相对应。另一方面,使用免疫印迹分析,在所有分析的细胞系中都检测到了α2-巨球蛋白。在免疫荧光试验中,在所有四个细胞系中也都检测到了α2-巨球蛋白,但染色模式不同。α2-巨球蛋白水平最低的U-536MG细胞的条件培养基对人成纤维细胞的促有丝分裂活性最低。