Dürr J, Lammi P, Goodman S L, Aigner T, von der Mark K
Max-Planck-Society, Clinical Research Unit for Rheumatology, Medical Clinic III, University of Erlange-Nürnberg, Germany.
Exp Cell Res. 1996 Jan 10;222(1):225-33. doi: 10.1006/excr.1996.0028.
In a previous study on the role of integrins in the interaction of human chondrocytes with extracellular collagen and fibronectin (Dürr et al., (1993) Exp. Cell Res. 207, 235) we showed that chondrocytes adhere to laminin-1 (LN-1) in a beta 1-integrin-dependent manner. FACS analysis with various integrin antibodies including the monoclonal antibody GOH3 indicated the presence of the alpha 6 beta 1-laminin receptor on the chondrocyte surface. Anti-alpha 6 antibodies inhibited adhesion to the LN-1/E8 fragment, but not to whole laminin or heat-denatured Laminin-1, indicating that chondrocytes utilize at least two beta 1-integrins for laminin adhesion, one of which is alpha 6 beta 1 recognizing the LN-1/E8 fragment. The presence of alpha 6 beta 1-integrin on the chondrocyte surface also suggested the existence of laminin-like molecules in cartilage. Here we provide immunological and biochemical evidence in support of this possibility. Several polyclonal antibodies raised against laminin-1 or the LN-1/E8 fragment revealed a strong pericellular reaction in sections of human fetal epiphyseal cartilage and adult articular cartilage. In the fetal epiphysis laminin staining was most prominent in mature, large chondrocytes appearing in the secondary ossification zone, in particular, in the vicinity of invading capillary sprouts. Chondrocytes in the proliferating and hypertrophic zone of the growth plate and perichondrium cells were negative. All chondrocytes that stained for alpha 6-integrin also stained for laminin-1. A laminin-1-like molecule was extracted from hyaline cartilage with two bands migrating slightly faster than the alpha 1 and beta 1/gamma 1 subunits of laminin on SDS-gel electrophoresis. The two bands stained with anti-laminin-1 antibodies and could be immunoprecipitated with the same antibodies from metabolically labeled chondrocyte cultures. These findings suggests a role for laminin in developing cartilage and thus additional roles for laminins outside basement membranes.
在先前一项关于整合素在人软骨细胞与细胞外胶原蛋白和纤连蛋白相互作用中作用的研究中(Dürr等人,(1993)《实验细胞研究》207, 235),我们发现软骨细胞以β1整合素依赖的方式黏附于层粘连蛋白-1(LN-1)。使用包括单克隆抗体GOH3在内的多种整合素抗体进行的流式细胞术分析表明,软骨细胞表面存在α6β1层粘连蛋白受体。抗α6抗体抑制了对LN-1/E8片段的黏附,但不抑制对完整层粘连蛋白或热变性层粘连蛋白-1的黏附,这表明软骨细胞利用至少两种β1整合素来进行层粘连蛋白黏附,其中一种是识别LN-1/E8片段的α6β1。软骨细胞表面α6β1整合素的存在也提示软骨中存在层粘连蛋白样分子。在此我们提供免疫和生化证据来支持这种可能性。几种针对层粘连蛋白-1或LN-1/E8片段产生的多克隆抗体在人胎儿骨骺软骨和成人关节软骨切片中显示出强烈的细胞周围反应。在胎儿骨骺中,层粘连蛋白染色在出现在次级骨化区的成熟大软骨细胞中最为明显,特别是在侵入的毛细血管芽附近。生长板增殖和肥大区的软骨细胞以及软骨膜细胞呈阴性。所有对α6整合素染色的软骨细胞也对层粘连蛋白-1染色。从透明软骨中提取出一种层粘连蛋白-1样分子,在SDS凝胶电泳上有两条带,迁移速度略快于层粘连蛋白的α1和β1/γ1亚基。这两条带用抗层粘连蛋白-1抗体染色,并且可以用相同抗体从代谢标记的软骨细胞培养物中进行免疫沉淀。这些发现表明层粘连蛋白在软骨发育中起作用,因此层粘连蛋白在基底膜外还有其他作用。