Brysk M M, Snider J M
J Invest Dermatol. 1982 Sep;79(3):193-7. doi: 10.1111/1523-1747.ep12500055.
The Concanavalin A reactive glycoproteins of epidermal cells were analyzed by the application of the iodinated lectin to molecules separated by SDS-PAGE. Normal epidermal cells were maintained as undifferentiated or differentiated by controlling the Ca++ concentration of the growth medium. Some 20 labeled bands could be resolved. Their relative intensities changed dramatically with the stage of differentiation. Fresh tissue gave a radioactive profile similar to that for cultured differentiated cells, except for evidence of damage from the techniques used to separate the epidermis from the dermis (the damage being progressively more severe going from heat to ammonium chloride to trypsin separation). The labeling patterns for three carcinogen-transformed cell lines were markedly different from those of the normal cells. The least tumorigenic cell line had a profile in many respects intermediate between those of the normal differentiated and undifferentiated cells, while the other 2 lines showed greater deviation.
通过将碘化凝集素应用于经十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)分离的分子,对表皮细胞的刀豆球蛋白A反应性糖蛋白进行了分析。通过控制生长培养基中的钙离子浓度,将正常表皮细胞维持在未分化或分化状态。大约可以分辨出20条标记带。它们的相对强度随分化阶段而显著变化。新鲜组织给出的放射性图谱与培养的分化细胞相似,但存在用于从真皮分离表皮的技术造成损伤的迹象(从加热到氯化铵再到胰蛋白酶分离,损伤逐渐加重)。三种致癌物转化细胞系的标记模式与正常细胞明显不同。致癌性最低的细胞系在许多方面的图谱介于正常分化和未分化细胞之间,而其他两个细胞系则表现出更大的偏差。