Masters J R, Petzoldt J L
Institute of Urology and Nephrology, University College London.
Verh Dtsch Ges Pathol. 1993;77:157-60.
Three methods for the culture of human urothelial cells in vitro are described: (1) the propagation of primary cultures and cell lines derived from normal urothelial cells, (2) the immortalization of normal urothelial cell lines with a temperature-sensitive SV40 large T antigen and (3) continuous cell lines derived from bladder cancers. Such cultures provide model systems for studying the factors that control the growth and differentiation of both normal and neoplastic urothelial cells, and for defining the morphological, biochemical and genetic changes associated with the development and progression of bladder cancer.
(1)原代培养及源自正常膀胱上皮细胞的细胞系的增殖;(2)用温度敏感型SV40大T抗原使正常膀胱上皮细胞系永生化;(3)源自膀胱癌的连续细胞系。此类培养物为研究控制正常和肿瘤性膀胱上皮细胞生长及分化的因素,以及确定与膀胱癌发生和进展相关的形态学、生化和遗传学变化提供了模型系统。