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评估培养的牛膀胱上皮细胞的分化状态:分层相关角蛋白K5和K6的合成增加以及尿血小板膜蛋白I的持续表达。

Assessing the differentiation state of cultured bovine urothelial cells: elevated synthesis of stratification-related K5 and K6 keratins and persistent expression of uroplakin I.

作者信息

Surya B, Yu J, Manabe M, Sun T T

机构信息

Department of Urology, Kaplan Cancer Center, New York University School of Medicine, NY 10016.

出版信息

J Cell Sci. 1990 Nov;97 ( Pt 3):419-32. doi: 10.1242/jcs.97.3.419.

DOI:10.1242/jcs.97.3.419
PMID:1705940
Abstract

Although significant progress has recently been made in culturing mammalian urothelial cells, relatively little is known about their biochemical differentiation. In this paper, we assessed the differentiation state of cultured bovine urothelial cells by analyzing their keratins and a cell surface marker, uroplakin I. Urothelial cells were serially cultured either in a serum-free medium, or in a serum-containing medium in the presence of 3T3 feeder cells, with similar results. Despite their stratified appearance, both normal urothelium and cultured urothelial cells synthesize mainly K8, K18 and K19, keratins that are typically seen in simple epithelia. However, cultured urothelial cells synthesize a greatly increased amount of K5 and K6 keratins, which are usually expressed by stratified epithelia but present only in trace amounts in normal urothelium. These data indicate that, as far as keratin synthesis is concerned, cultured urothelial cells undergo an altered pattern of differentiation towards a more 'stratified phenotype'; this unusual finding has interesting implications for urothelial evolution. In the meantime, many superficial cells in cultured urothelial colonies make uroplakin I, a 27 x 10(3) Mr protein subunit of the asymmetrical unit membrane (AUM) characteristic of urothelial (superficial) umbrella cells. These results indicate that cultured urothelial cells undergo, at least in part, AUM biogenesis. Cultured urothelial cells thus provide a useful experimental model system for studying certain early steps of AUM formation.

摘要

尽管最近在培养哺乳动物尿路上皮细胞方面取得了重大进展,但对其生化分化的了解相对较少。在本文中,我们通过分析培养的牛尿路上皮细胞的角蛋白和一种细胞表面标志物uroplakin I来评估其分化状态。尿路上皮细胞在无血清培养基中连续培养,或在含有3T3饲养细胞的含血清培养基中连续培养,结果相似。尽管它们呈现分层外观,但正常尿路上皮和培养的尿路上皮细胞主要合成K8、K18和K19,这些角蛋白通常见于单层上皮。然而,培养的尿路上皮细胞合成的K5和K6角蛋白量大幅增加,这两种角蛋白通常由复层上皮表达,但在正常尿路上皮中仅微量存在。这些数据表明,就角蛋白合成而言,培养的尿路上皮细胞经历了向更“复层表型”的分化模式改变;这一不寻常的发现对尿路上皮的进化具有有趣的意义。与此同时,培养的尿路上皮细胞集落中的许多表层细胞产生uroplakin I,这是尿路上皮(表层)伞细胞不对称单位膜(AUM)的一种27×10³Mr蛋白亚基。这些结果表明,培养的尿路上皮细胞至少部分经历了AUM生物发生。因此,培养的尿路上皮细胞为研究AUM形成的某些早期步骤提供了一个有用的实验模型系统。

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