Braunewell K H, Pesheva P, McCarthy J B, Furcht L T, Schmitz B, Schachner M
Department of Neurobiology, Swiss Federal Institute of Technology, Hönggerberg, Zürich.
Eur J Neurosci. 1995 Apr 1;7(4):805-14. doi: 10.1111/j.1460-9568.1995.tb00683.x.
We have previously described two proteoglycans from human sciatic nerve which are immunochemically related to the chondroitin sulphate proteoglycans versican and decorin. The chondroitin sulphate of the versican-like molecule and the core protein of the decorin-like molecule have been found previously to be up-regulated after lesioning the adult mouse sciatic nerve. To investigate if the versican- and decorin-like molecules are involved in cell-extracellular matrix interactions, we studied the effect of both molecules on cell adhesion. The versican- and decorin-like molecules, substrate-coated in a mixture with fibronectin, but not with laminin or collagen types I or IV, inhibited the adhesion of several cell lines, neonatal dorsal root ganglion neurons and Schwann cells. The inhibitory activity was concentration-dependent and mediated by the chondroitin sulphate. Furthermore, when different proteoglycans were incubated with fibronectin, only the versican- and decorin-like molecules and the chondroitin sulphate proteoglycan aggrecan, but not the heparan sulphate proteoglycan perlecan, were able to inhibit fibronectin-mediated cell adhesion. The versican- and decorin-like molecules, substrate-coated alone or in a mixture with fibronectin or laminin, were at most slightly inhibitory to neurite outgrowth from PC12 phaeochromocytoma cells and neonatal dorsal root ganglion neurons. In a solid-phase ligand-binding assay the versican- and decorin-like molecules interacted with fibronectin, but not with laminin or collagen types I and IV. Binding of the versican-like molecule to fibronectin and inhibition of cell adhesion by this molecule was mediated via the heparin and cell-binding domains of fibronectin. These observations suggest that binding of the two proteoglycans to fibronectin is involved in the modulation of adhesion of cells to fibronectin.
我们之前描述过从人坐骨神经中提取的两种蛋白聚糖,它们在免疫化学上与硫酸软骨素蛋白聚糖多功能蛋白聚糖和核心蛋白聚糖相关。先前已发现,成年小鼠坐骨神经损伤后,多功能蛋白聚糖样分子的硫酸软骨素和核心蛋白聚糖样分子的核心蛋白会上调。为了研究多功能蛋白聚糖样分子和核心蛋白聚糖样分子是否参与细胞与细胞外基质的相互作用,我们研究了这两种分子对细胞黏附的影响。多功能蛋白聚糖样分子和核心蛋白聚糖样分子与纤连蛋白混合包被在底物上,但与层粘连蛋白或I型或IV型胶原混合包被时则不然,它们抑制了几种细胞系、新生背根神经节神经元和雪旺细胞的黏附。抑制活性呈浓度依赖性,且由硫酸软骨素介导。此外,当不同的蛋白聚糖与纤连蛋白一起孵育时,只有多功能蛋白聚糖样分子、核心蛋白聚糖样分子和硫酸软骨素蛋白聚糖聚集蛋白聚糖能够抑制纤连蛋白介导的细胞黏附,而硫酸乙酰肝素蛋白聚糖基底膜聚糖则不能。多功能蛋白聚糖样分子和核心蛋白聚糖样分子单独包被或与纤连蛋白或层粘连蛋白混合包被在底物上时,对PC12嗜铬细胞瘤细胞和新生背根神经节神经元的神经突生长最多只有轻微的抑制作用。在固相配体结合试验中,多功能蛋白聚糖样分子和核心蛋白聚糖样分子与纤连蛋白相互作用,但不与层粘连蛋白或I型和IV型胶原相互作用。多功能蛋白聚糖样分子与纤连蛋白的结合以及该分子对细胞黏附的抑制作用是通过纤连蛋白的肝素结合域和细胞结合域介导的。这些观察结果表明,这两种蛋白聚糖与纤连蛋白的结合参与了细胞与纤连蛋白黏附的调节。