Wood P, Okada E, Bunge R
Brain Res. 1980 Aug 25;196(1):247-52. doi: 10.1016/0006-8993(80)90732-5.
A neuronal culture system has been developed that has the demonstrated ability to induce myelin formation by added oligodendrocytes. Networks of dissociated dorsal root ganglion neurons were prepared by suppressing non-neuronal cells (i.e. fibroblasts and Schwann cells) with a continuous 2 week exposure to 10(-5)M fluorodeoxyuridine in the culture medium. After drug withdrawal, neuroglial cells were introduced in optic nerve implants from 1-2 week-old rats. These added glial cells migrated extensively over the unensheathed neurites and central myelin was formed by 2 weeks after the implant addition.
已开发出一种神经元培养系统,该系统已证明有能力通过添加少突胶质细胞诱导髓鞘形成。通过在培养基中连续2周暴露于10^(-5)M氟脱氧尿苷来抑制非神经元细胞(即成纤维细胞和雪旺细胞),从而制备解离的背根神经节神经元网络。撤药后,将神经胶质细胞引入1-2周龄大鼠的视神经植入物中。这些添加的神经胶质细胞在无髓鞘的神经突上广泛迁移,并且在植入后2周形成中枢髓鞘。