Cellular proliferation in the crypt epithelium of human small intestinal xenografts.

Epithelial cell biology Pub Date : 1995-01-01
A N Shmakov, T C Savidge
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引用次数: 0

Abstract

The present study investigates the spatial organisation of epithelial cell proliferation in human small intestinal xenografts, in order that direct comparisons can be made with paediatric small bowel. For this purpose we employed the MIB-1 (Ki-67) monoclonal antibody and [3H]thymidine to analyse the crypt growth fraction and DNA synthesising (S-phase) cells, respectively. The spatial distribution of cycling (MIB-1+) cells was appropriately confined to the xenograft crypts where it closely resembled that of paediatric intestine, both in terms of the labelling index and an ability to form runs of labelled cells, thereby demonstrating synchronous patterns of cell division. In addition, the S-phase representation in xenograft intestine was uniform throughout the crypt proliferation compartment thereby indicating cell-cycle homogeneity. This chimeric model system now provides a new approach to investigate altered proliferative responses of human gut to a number of potentially harmful substances e.g. carcinogens, the assessment of which is not feasible in patients or volunteers.

人小肠异种移植物隐窝上皮细胞增殖。
本研究调查了人小肠异种移植上皮细胞增殖的空间组织,以便与儿科小肠进行直接比较。为此,我们使用了mb -1 (Ki-67)单克隆抗体和[3H]胸腺嘧啶分别分析了隐窝生长部分和DNA合成(s期)细胞。循环(mb -1+)细胞的空间分布被适当地限制在异种移植物隐窝中,在标记指数和形成标记细胞群的能力方面,它与儿科肠道非常相似,从而显示出细胞分裂的同步模式。此外,异种移植肠的s期表现在整个隐窝增殖室中是均匀的,从而表明细胞周期的同质性。这种嵌合模型系统现在提供了一种新的方法来研究人类肠道对一些潜在有害物质(如致癌物)的增殖反应的改变,对这些物质的评估在患者或志愿者中是不可实现的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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