Baron-Van Evercooren A, Kleinman H K, Seppä H E, Rentier B, Dubois-Dalcq M
J Cell Biol. 1982 Apr;93(1):211-6. doi: 10.1083/jcb.93.1.211.
Techniques are now available for culturing well characterized and purified Schwann cells. Therefore, we investigated the role of fibronectin in the adhesion, growth, and migration of cultured rat Schwann cells. Double-immunolabeling shows that, in primary cultures of rat sciatic nerve, Schwann cells (90%) rarely express fibronectin, whereas fibroblasts (10%) exhibit a granular cytoplasmic and fibrillar surface-associated fibronectin. Secondary cultures of purified Schwann cells do not express fibronectin. Exogenous fibronectin has a small effect on promoting the adhesion of Schwann cells to the substrate and does not significantly affect cell morphology, but it produced a surface fibrillar network on fibronectin on the secondary Schwann cells. Tritiated thymidine autoradiography revealed that addition of fibronectin to the medium, even at low concentrations, markedly stimulates Schwann cell proliferation, in both primary and secondary cultures. In addition, when cell migration was measured in a Boyden chamber assay, fibronectin was found to moderately, but clearly, stimulate directed migration or chemotaxis.
现在已有技术可用于培养特性明确且纯化的施万细胞。因此,我们研究了纤连蛋白在培养的大鼠施万细胞的黏附、生长和迁移中的作用。双重免疫标记显示,在大鼠坐骨神经的原代培养物中,施万细胞(90%)很少表达纤连蛋白,而成纤维细胞(10%)呈现颗粒状细胞质和与表面纤维相关的纤连蛋白。纯化施万细胞的传代培养物不表达纤连蛋白。外源性纤连蛋白对促进施万细胞与底物的黏附作用较小,且对细胞形态无显著影响,但它在传代施万细胞的纤连蛋白上产生了表面纤维网络。氚标记胸腺嘧啶核苷放射自显影显示,即使在低浓度下,向培养基中添加纤连蛋白也能显著刺激原代和传代培养物中施万细胞的增殖。此外,当在博伊登室试验中测量细胞迁移时,发现纤连蛋白能适度但明显地刺激定向迁移或趋化性。