Elhamady M S, Hopwood D, Milne G, Ross P, Bouchier I A
J Pathol. 1983 Jul;140(3):221-35. doi: 10.1002/path.1711400305.
Tissue culture of gall-bladder was attempted in the following media: Dulbecco, Eagle's minimum essential medium, NCTC 135, medium 199 and Ham's F12. Growth occurred in all of them for up to 2 weeks assessed by light microscopy. No enhancement of growth was induced by collagenase trypsin insulin or hydrocortisone. Scanning electron microscopy confirmed that new cells colonised the free surface of the explant. Transmission electron microscopy showed good preservation of the original tall epithelial cells for the period of study. The new migrating cells were flatter, but retained the morphological features of the columnar cells. Secretory granules were absent after 1 day in culture but increased amounts of glycogen and lipid began to appear in the epithelium.
杜尔贝科氏培养基、伊格尔氏最低限度基本培养基、NCTC 135培养基、199培养基和哈姆氏F12培养基。通过光学显微镜评估,在所有这些培养基中,细胞生长可持续长达2周。胶原酶、胰蛋白酶、胰岛素或氢化可的松均未诱导生长增强。扫描电子显微镜证实新细胞定殖在外植体的游离表面。透射电子显微镜显示在研究期间原始高柱状上皮细胞保存良好。新迁移的细胞更扁平,但保留了柱状细胞的形态特征。培养1天后分泌颗粒消失,但上皮中糖原和脂质的量开始增加。