Handler J S, Preston A S, Steele R E
Fed Proc. 1984 May 15;43(8):2221-4.
Under standard culture conditions, epithelial cells grow with their basal surface attached to the culture dish and their apical surface facing the medium. Morphological and functional markers are located in the appropriate plasma membrane, and transepithelial transport occurs in a variety of cultured epithelia. As a result of the polarity of the cells and the presence of tight junctions between cells, on standard tissue culture dishes there is restricted access of growth medium to the basolateral surface of the epithelium, which is the surface at which nutrient exchange normally occurs. Greater differentiation of epithelial cultures can be achieved by growing primary cultures or continuous cell lines on permeable surfaces such as porous bottom cultures dishes in which the porous bottom is formed by a filter or membrane of collagen, or on floating collagen gels. In many cultures, differentiation varies with the time after the culture was seeded. Certain chemicals that accelerate differentiation in nonepithelial cells also accelerate the differentiation of epithelial cultures. Ultimately, defined media and specific substrates for cell attachment should lead to further differentiation of epithelia in culture.
在标准培养条件下,上皮细胞生长时其基底表面附着于培养皿,顶端表面朝向培养基。形态学和功能标记物位于合适的质膜中,并且跨上皮运输发生在多种培养的上皮组织中。由于细胞的极性以及细胞间紧密连接的存在,在标准组织培养皿上,生长培养基难以接触到上皮组织的基底外侧表面,而营养物质交换通常发生在该表面。通过在可渗透表面(如多孔底部培养皿,其多孔底部由胶原过滤器或膜形成)或漂浮的胶原凝胶上培养原代培养物或连续细胞系,可以实现上皮培养物的更大程度分化。在许多培养物中,分化随接种后时间而变化。某些能加速非上皮细胞分化的化学物质也能加速上皮培养物的分化。最终,确定的培养基和用于细胞附着的特定底物应能使培养的上皮组织进一步分化。