Bähr M, Hopkins J M, Bunge R P
Neurologische Universitätsklinik, Tübingen, Germany.
Glia. 1991;4(5):529-33. doi: 10.1002/glia.440040512.
Schwann cell cultures provide a highly favorable substrate for retinal ganglion cell (RGC) survival and axon growth in vitro (Bähr and Bunge, Exp Neurol 106:27, 1989; Hopkins and Bunge, Glia 4:46, 1991). In this report we have extended former studies to obtain axon regeneration, long-term survival, and myelination of adult rat RGC axons in co-cultures of retinal explants with purified Schwann cells. By using modified co-culture conditions, we observed myelination of regenerating adult RGC axons by Schwann cells after 3-4 weeks in vitro. Myelination was associated with a one-to-one Schwann cell-axon relationship, characteristic of the formation of peripheral myelin. Under culture conditions that supported myelination, long-term survival (more than 12 weeks) of a small population of RGCs was observed. These findings highlight the remarkable ability of Schwann cells to support long-term survival of adult rat RGCs in the absence of either central nervous system (CNS) target tissue or other peripheral nervous system (PNS) components. This tissue culture system may serve as a model for the systematic study of the molecular mechanisms which are involved in axon regeneration and myelination of adult CNS neurons.
施万细胞培养物为视网膜神经节细胞(RGC)在体外的存活和轴突生长提供了极为有利的底物(Bähr和Bunge,《实验神经病学》106:27,1989;Hopkins和Bunge,《神经胶质》4:46,1991)。在本报告中,我们扩展了先前的研究,以在视网膜外植体与纯化的施万细胞的共培养物中实现成年大鼠RGC轴突的轴突再生、长期存活和髓鞘形成。通过使用改良的共培养条件,我们观察到在体外培养3 - 4周后,施万细胞对成年RGC再生轴突进行了髓鞘形成。髓鞘形成与施万细胞 - 轴突一对一的关系相关,这是外周髓鞘形成的特征。在支持髓鞘形成的培养条件下,观察到一小部分RGC能够长期存活(超过12周)。这些发现突出了施万细胞在没有中枢神经系统(CNS)靶组织或其他外周神经系统(PNS)成分的情况下支持成年大鼠RGC长期存活的显著能力。这种组织培养系统可作为一个模型,用于系统研究参与成年CNS神经元轴突再生和髓鞘形成的分子机制。