Johnson J E, Turner J E
J Neurosci Res. 1982;8(2-3):315-29. doi: 10.1002/jnr.490080221.
The minimal requirements for the regeneration of optic nerve fibers in vitro were established in a serum-free retinal explant preparation. This serum-free preparation was developed as a prerequisite for testing the growth-promoting activity of tissue extracts prepared from the primary target of regenerating fibers. Explants taken from goldfish retinas 14 days after a prior optic nerve crush were capable of long-term survival and regenerated neurite outgrowth without serum or hormonal supplements. Serum-free conditions for explant outgrowth required only a basic Leibovitz (L-15) media containing 0.6% methyl cellulose (MC). Explants were also capable of neurite outgrowth in L-15 media alone when culture dishes were preplated with MC. MC treatment permitted both the regeneration of neurites in serum-free L-15 and a significant increase in the rate and extent of neurite outgrowth when combined with 10% fetal calf serum (FCS). Explants grown in L-15 with both MC and FCS produced a 2.5-fold increase in the length of neurite outgrowth over MC alone and a 1.5-fold increase in the length of neurite outgrowth over FCS alone. MC activity which permitted minimal serum-free regeneration and optimal serum supplemented regeneration was determined to be substrate related. Retinas were dissociated to determine if ganglion cells, like the intact explant, were capable of survival and neurite regeneration in serum-free conditions. These cells survived and extended long neurites when grown in L-15 with FCS or with FCS and MC, but they did not survive in serum-free L-15 with MC. The minimal serum-free conditions for explant survival and neurite regeneration were used as a model system to test the growth-promoting activity of crude tissue extracts prepared from the goldfish brain. Extracts prepared from the primary target region, the optic tectum, stimulated a significant 2.5-fold increase in the length of regenerating neurites. The optic tectal extract (OTex) stimulated outgrowth with significantly high specific activity when compared with extracts of identical protein concentrations prepared from the cerebellum (Cex). At a minimal protein concentration of 150 micrograms/ml, the OTex stimulated a 1.5-fold increase in neurite outgrowth above Cex. These results indicated that a serum-free culture preparation had been established for optic nerve regeneration. This culture system has proven to be an extremely sensitive bioassay model without the masking effect of a serum supplement. Serum-free cultures may be used in further studies to determine the role neurotrophic factors may play in a widely used model of successful central nervous system (CNS) regeneration.
在无血清视网膜外植体制备中确定了体外视神经纤维再生的最低要求。这种无血清制备方法是作为测试从再生纤维的主要目标制备的组织提取物的促生长活性的前提条件而开发的。在先前视神经挤压14天后从金鱼视网膜取出的外植体能够长期存活,并且在没有血清或激素补充剂的情况下再生神经突生长。外植体生长的无血清条件仅需要含有0.6%甲基纤维素(MC)的基本莱博维茨(L-15)培养基。当培养皿预先用MC包被时,外植体在单独的L-15培养基中也能够进行神经突生长。MC处理既允许在无血清L-15中神经突再生,又在与10%胎牛血清(FCS)联合使用时显著提高神经突生长的速率和程度。在含有MC和FCS的L-15中生长的外植体,其神经突生长长度比单独使用MC增加了2.5倍,比单独使用FCS增加了1.5倍。确定允许最低限度无血清再生和最佳血清补充再生的MC活性与底物有关。分离视网膜以确定神经节细胞是否像完整外植体一样,在无血清条件下能够存活和神经突再生。当这些细胞在含有FCS或含有FCS和MC的L-15中生长时,它们存活并伸出长神经突,但在含有MC的无血清L-15中不能存活。外植体存活和神经突再生的最低无血清条件被用作模型系统,以测试从金鱼脑制备的粗组织提取物的促生长活性。从主要目标区域视顶盖制备的提取物刺激再生神经突长度显著增加2.5倍。与从小脑(Cex)制备的相同蛋白质浓度的提取物相比,视顶盖提取物(OTex)以显著高的比活性刺激生长。在最低蛋白质浓度为150微克/毫升时,OTex刺激神经突生长比Cex增加了1.5倍。这些结果表明已经建立了用于视神经再生的无血清培养制备方法。这种培养系统已被证明是一种极其敏感的生物测定模型,没有血清补充剂的掩盖作用。无血清培养可用于进一步研究,以确定神经营养因子在广泛使用的成功中枢神经系统(CNS)再生模型中可能发挥的作用。