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由蜗牛Helisoma特定中枢神经系统组织条件培养液产生的神经生长促进因子。

Nerve growth-promoting factor produced in culture media conditioned by specific CNS tissues of the snail Helisoma.

作者信息

Wong R G, Barker D L, Kater S B, Bodnar D A

出版信息

Brain Res. 1984 Jan 30;292(1):81-91. doi: 10.1016/0006-8993(84)90892-8.

Abstract

Medium conditioned by tissue from the CNS of the snail, Helisoma, is capable of promoting neurite outgrowth in isolated neurons from adult central ganglia. The conditioning factor(s) (CF), contained in conditioned medium (CM), is produced only by central ganglionic rings and buccal ganglia and not by other tissues, including hemolymph. CF requires a minimum of 24 h to be produced or released into the medium. At 12 h growth-promoting activity was not detectable. CF binds tightly to the polylysine substratum and its activity is not mimicked by addition of various sera, NGF or fibronectin. CF activity is abolished by chymotrypsin, trypsin or heating to 100 degrees C, but is stable to DNase and RNase treatment. The percentage of cells exhibiting neurite outgrowth is approximately linear with the amount of neural tissue used to condition the medium up to 2 ganglionic rings/ml. Addition of more ganglia fails to stimulate a greater response. This apparent plateau of CM activity appears to be a function of production and/or release of CF, rather than a saturation effect on plated cells, since dose-response curves for dilutions of CM are approximately linear regardless of the number of ganglia used for conditioning. In addition, anisomycin inhibits 35% of CF appearance under conditions of over 90% protein synthesis inhibition in the ganglia used to produce the CM. Under these conditions anisomycin has no apparent effect on the maintenance of electrical excitability. The inhibitor data suggest that 65% of CF is derived from a pre-existing storage pool and that the remainder is synthesized during the 72 h conditioning period.

摘要

由蜗牛(Helisoma)中枢神经系统组织所调节的培养基,能够促进成年中枢神经节分离神经元的神经突生长。调节培养基(CM)中所含的调节因子(CF)仅由中枢神经节环和颊神经节产生,而非其他组织,包括血淋巴。CF产生或释放到培养基中至少需要24小时。在12小时时,未检测到促生长活性。CF与聚赖氨酸基质紧密结合,其活性不能通过添加各种血清、神经生长因子(NGF)或纤连蛋白来模拟。CF活性可被胰凝乳蛋白酶、胰蛋白酶或加热至100℃消除,但对脱氧核糖核酸酶(DNase)和核糖核酸酶(RNase)处理稳定。表现出神经突生长的细胞百分比与用于调节培养基的神经组织量大致呈线性关系,最高可达2个神经节环/毫升。添加更多神经节并不能刺激更大的反应。CM活性的这种明显平台期似乎是CF产生和/或释放的函数,而不是对平板细胞的饱和效应,因为无论用于调节的神经节数量如何,CM稀释液的剂量反应曲线大致呈线性。此外,茴香霉素在用于产生CM的神经节中蛋白质合成抑制超过90%的条件下,抑制35%的CF出现。在这些条件下,茴香霉素对电兴奋性的维持没有明显影响。抑制剂数据表明,65%的CF来自预先存在的储存池,其余部分在72小时的调节期内合成。

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