Zhu X J, Eisinger M, Bystryn J C
J Invest Dermatol. 1984 Nov;83(5):340-3. doi: 10.1111/1523-1747.ep12264322.
Macromolecules expressed on the external surface of human keratinocytes in tissue culture were radioiodinated by the lactoperoxidase technique and solubilized by lysing the cells in nonionic detergent. Soluble labeled proteins were characterized by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The pattern of proteins expressed by keratinocytes was distinct for these cells. The major labeled components had Mrs of 28K, 40K, 68K, 72K, and 77K. The expression of several macromolecules changed with the length of time the cells were in culture, suggesting that their expression was linked to epidermal differentiation. Lastly, many but not all of the macromolecules expressed on the surface of keratinocytes were selectively and rapidly released into medium by the cells.
采用乳过氧化物酶技术对组织培养中人类角质形成细胞外表面表达的大分子进行放射性碘化,并通过在非离子去污剂中裂解细胞使其溶解。用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳对可溶性标记蛋白进行表征。角质形成细胞表达的蛋白质模式对于这些细胞来说是独特的。主要的标记成分的分子量分别为28K、40K、68K、72K和77K。几种大分子的表达随着细胞培养时间的延长而变化,这表明它们的表达与表皮分化有关。最后,角质形成细胞表面表达的许多(但不是全部)大分子被细胞选择性地快速释放到培养基中。