鉴定85-100 kDa糖蛋白作为尿路上皮分化晚期的细胞表面标志物:与斑块间(“铰链”)区域相关。

Epithelial cell biology Pub Date : 1992-01-01
J Yu, M Manabe, T T Sun
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引用次数: 0

摘要

尽管膀胱癌占所有人类癌症死亡的近5%,但对尿路上皮分化的生物化学知之甚少。我们最近确定了不对称单位膜(AUM)的三个主要蛋白质亚基(“uroplakins”),它们形成坚硬的斑块,覆盖了尿路上皮浅(伞)细胞顶端表面的70%。连接这些斑块的普通质膜被认为在功能上是专门的,作为灵活而耐用的“铰链”。这些铰链膜是否具有生物化学上的独特性尚不清楚。使用一种新的单克隆抗体(AE32),我们已经鉴定出一个85-100 kDa的糖蛋白(UGP85),它似乎是尿路特异性的。在正常尿路上皮和培养的尿路上皮菌落中,这种细胞表面蛋白主要与浅表细胞相关,表明其表达依赖于分化。体外翻译实验结果表明,该糖蛋白含有一个约55 kDa的核心多肽。利用免疫金定位技术,我们发现在培养的尿路上皮菌落(已知缺乏成熟的AUM斑块)中,UGP85相对均匀地分布在一些分化细胞的根尖表面。然而,在正常尿路上皮的浅表细胞中,UGP85主要与铰链区相关。这些结果提出了一种可能性,即UGP85是一种质膜成分,可以在不同程度上从斑块区域排除,因为12 nm的蛋白质颗粒被组装成紧密排列的准晶AUM结构。UGP85的鉴定提供了第一个证据,证明连接尿路上皮斑块的铰链区域与下层细胞层相对未分化的尿路上皮细胞的质膜具有生物化学区别。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of an 85-100 kDa glycoprotein as a cell surface marker for an advanced stage of urothelial differentiation: association with the inter-plaque ('hinge') area.

Although bladder cancers account for almost 5% of all human cancer deaths, little is known about the biochemistry of urothelial differentiation. We have recently identified three major protein subunits ('uroplakins') of asymmetric unit membranes (AUM), which form rigid-looking plaques covering up to 70% of the apical surface of urothelial superficial (umbrella) cells. The ordinary-looking plasma membranes that interconnect these plaques are believed to be functionally specialized, serving as flexible but durable 'hinges'. Whether these hinge membranes are biochemically unique is unknown. Using a new monoclonal antibody (AE32) we have identified an 85-100 kDa glycoprotein (UGP85) which appears to be urothelium-specific. In both normal urothelium and cultured urothelial colonies this cell surface protein is associated mainly with superficial cells, suggesting that its expression is differentiation dependent. Results from in vitro translation experiments indicated that this glycoprotein contains a core polypeptide of about 55 kDa. Using immunogold localization techniques, we showed that in cultured urothelial colonies--which are known to lack mature AUM plaques--UGP85 is distributed relatively uniformly on the apical surface of some differentiated cells. However, in superficial cells of normal urothelium UGP85 is mainly associated with the hinge areas. These results raise the possibility that UGP85 is a plasma membrane component which can be excluded, to varying extents, from the plaque region as 12 nm protein particles are assembled into a tightly packed paracrystalline AUM structure. The identification of UGP85 provides the first evidence that the hinge areas interconnecting the urothelial plaques are biochemically distinguishable from the plasma membranes of the relatively undifferentiated urothelial cells of the lower cell layers.(ABSTRACT TRUNCATED AT 250 WORDS)

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