Quondamatteo F, Kempkensteffen C, Miosge N, Sonnenberg A, Herken R
Department of Histology, University of Goettingen, Goettingen, Germany.
Histol Histopathol. 2004 Jul;19(3):799-806. doi: 10.14670/HH-19.799.
Normal liver sinusoids are not lined by a basement membrane (BM). In contrast, in the course of development of liver cirrhosis, a structured BM is formed de novo in the space of Disse. This BM contributes to the inhibition of the metabolic function of the liver but the pathogenic background of the formation of this perisinusoidal BM is still unclear. Integrins of the beta1-class are generally essential for BM stability and some of them (such as alpha2beta1, alpha3beta1 and alpha6beta1) appear de novo in the perisinusoidal space of the cirrhotic liver. Their cellular distribution in capillarized sinusoids as well as the correlation between their cellular distribution and the formation of the microvascular BM in the cirrhotic liver has not been shown at the ultrastructural level. In the present work we aimed to clarify this issue. We focused on integrins alpha3beta1 and alpha6beta1 and localised them ultrastructurally in human cirrhotic liver microvessels using postembedding immunogold which allows the ultrastructural localization of antigens with high resolution in the tissue. The newly formed basement membrane of capillarized sinusoids was visualized by means of fixation with addition of tannic acid, which enables the visualization of structures of the extracellular matrix with the highest resolution. Also, we carried out laminin detection using postembedding immunogold. Our results show that both alpha3beta1 and alpha6beta1 are expressed on the surface of both hepatocytes and endothelial cells, i.e. on both sides of the newly formed basement membrane. This latter shows zones of higher density both in close proximity to the endothelial and to the hepatocytic surfaces which resemble laminae densae. We propose that hepatocytes and endothelial cells may, therefore, by expressing such integrins, contribute to the formation of this pathological BM in the microvessels of the human cirrhotic liver. On stellate cells, which are major producers of BM components, both integrins alpha3beta1 and alpha6beta1 were also localized.
正常肝血窦没有基底膜(BM)衬里。相反,在肝硬化发展过程中,狄氏间隙会重新形成结构化的基底膜。这种基底膜会抑制肝脏的代谢功能,但这种肝血窦周围基底膜形成的致病背景仍不清楚。β1类整合素通常对基底膜的稳定性至关重要,其中一些整合素(如α2β1、α3β1和α6β1)在肝硬化肝脏的肝血窦周围空间中新生出现。它们在毛细血管化血窦中的细胞分布以及它们的细胞分布与肝硬化肝脏中微血管基底膜形成之间的相关性在超微结构水平上尚未得到证实。在本研究中,我们旨在阐明这个问题。我们聚焦于整合素α3β1和α6β1,并使用包埋后免疫金标法在超微结构水平上定位它们在人类肝硬化肝脏微血管中的位置,这种方法能够在组织中以高分辨率对抗抗原进行超微结构定位。通过添加单宁酸固定来观察毛细血管化血窦新形成的基底膜,这能够以最高分辨率观察细胞外基质的结构。此外,我们还使用包埋后免疫金标法进行层粘连蛋白检测。我们的结果表明,α3β1和α6β1均在肝细胞和内皮细胞表面表达,即在新形成的基底膜两侧表达。后者在靠近内皮细胞和肝细胞表面处均显示出较高密度区域,类似于致密板层。因此,我们认为肝细胞和内皮细胞可能通过表达此类整合素,参与人类肝硬化肝脏微血管中这种病理性基底膜的形成。在作为基底膜成分主要产生者的星状细胞上,也定位到了整合素α3β1和α6β1。