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原发性胆汁性肝硬化中的胆管细胞处于易于凋亡的“致敏”状态。

Bile duct cells in primary biliary cirrhosis are 'primed' for apoptosis.

作者信息

Graham A M, Dollinger M M, Howie S E, Harrison D J

机构信息

University Department of Pathology, Edinburgh, UK.

出版信息

Eur J Gastroenterol Hepatol. 1998 Jul;10(7):553-7. doi: 10.1097/00042737-199807000-00005.

DOI:10.1097/00042737-199807000-00005
PMID:9855077
Abstract

OBJECTIVE

Primary biliary cirrhosis (PBC) is characterized by progressive, immune-mediated destruction of bile ducts (<75 microm diameter) and secondary changes related to cholestasis which may involve apoptosis. In this study we sought to examine the protein expression of genes involved in apoptosis in biliary epithelium of PBC cases.

DESIGN

In order to investigate the susceptibility of biliary epithelial cells to apoptosis and their ability to proliferate, we examined the expression of a number of apoptosis related proteins in early and late stage PBC and histologically normal liver control tissue using immunohistochemistry.

METHODS

Liver biopsies from 15 early (stages I and II) and 14 late (stages III and IV) cases of PBC and 15 normal cases were examined immunohistochemically for expression of p53, CD95/Fas, bax, bcl-x, bcl-2 and the proliferation marker Ki-67.

RESULTS

CD95/Fas, bax and bcl-x were identified in biliary epithelium in 8/15, 11/15 and 8/15 normal biopsies. Weak expression of bcl-2 was found, but p53 was not identified. In cases of PBC surviving bile ducts showed strong bax and bcl-x expression. Inflammatory infiltrates were strongly bcl-2 positive. In cases showing a marked ductular reaction there was increased reactivity for bax and bcl-x in ductules. No change in CD95/Fas or p53 expression was seen. An increase in Ki-67 positive biliary epithelial cells was seen in PBC cases, indicating cell cycle activity.

CONCLUSIONS

Bile duct epithelium constitutively expresses several genes involved in the execution of apoptosis but these cells also retain the ability to proliferate.

摘要

目的

原发性胆汁性肝硬化(PBC)的特征是进行性、免疫介导的胆管(直径<75微米)破坏以及与胆汁淤积相关的继发性改变,这可能涉及细胞凋亡。在本研究中,我们试图检测PBC患者胆管上皮中参与细胞凋亡的基因的蛋白表达。

设计

为了研究胆管上皮细胞对细胞凋亡的易感性及其增殖能力,我们使用免疫组织化学检测了早期和晚期PBC以及组织学正常的肝脏对照组织中多种凋亡相关蛋白的表达。

方法

对15例早期(I期和II期)和14例晚期(III期和IV期)PBC患者以及15例正常患者的肝活检组织进行免疫组织化学检测,以检测p53、CD95/Fas、bax、bcl-x、bcl-2的表达以及增殖标志物Ki-67。

结果

在15例正常活检组织的胆管上皮中,8例检测到CD95/Fas,11例检测到bax,8例检测到bcl-x。发现bcl-2表达较弱,但未检测到p53。在PBC病例中,存活的胆管显示出强烈的bax和bcl-x表达。炎性浸润bcl-2呈强阳性。在显示明显小胆管反应的病例中,小胆管中bax和bcl-x的反应性增加。未观察到CD95/Fas或p53表达的变化。在PBC病例中,Ki-67阳性的胆管上皮细胞增加,表明细胞周期活性。

结论

胆管上皮组成性表达几种参与细胞凋亡执行的基因,但这些细胞也保留了增殖能力。

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