Autrup H, Barrett L A, Jackson F E, Jesudason M L, Stoner G, Phelps P, Trump B F, Harris C C
Gastroenterology. 1978 Jun;74(6):1248-57.
Human colonic epithelium has been cultured as explants in a chemically defined medium for periods of 1 to 20 days. The viability of the explants was shown by the preservation of the ultrastructural features of the colonic epithelial cells and by active incorporation of radioactive precursors into cellular DNA and protein. A progressive decrease in the number of goblet cells, decrease in the depth of the crypts, and a change from a columnar to a cuboidal epithelium were observed. After 20 days in culture the colonic mucosa consisted of a single layer of cuboidal epithelial cells and a few glands. The ability to maintain colonic mucosa in culture was subject to both intra- and interindividual variation. Cultured human colonic mucosa also activated a chemical procarcinogen, benzo[a]pyrene, into metabolites which bound to cellular DNA. A 100-fold interindividual variation in this binding was observed.
人结肠上皮已作为外植体在化学成分明确的培养基中培养1至20天。外植体的活力通过结肠上皮细胞超微结构特征的保留以及放射性前体活跃掺入细胞DNA和蛋白质得以体现。观察到杯状细胞数量逐渐减少、隐窝深度降低以及上皮从柱状变为立方状。培养20天后,结肠黏膜由单层立方上皮细胞和少数腺体组成。在培养中维持结肠黏膜的能力存在个体内和个体间差异。培养的人结肠黏膜还能将化学致癌物苯并[a]芘激活为与细胞DNA结合的代谢产物。观察到这种结合存在100倍的个体间差异。