Varon S, Skaper S D, Manthorpe M
Brain Res. 1981 Jan;227(1):73-87. doi: 10.1016/0165-3806(81)90095-x.
We describe here the use of 3 established nerve growth factor (NGF) targets (cultured neurons from dissociated chick embryo sympathetic ganglia, and chick embryo or neonatal mouse dorsal root ganglia) to investigate neuronotrophic activities in conditioned media (CMs) from: (i) chick embryo heart; (ii) purified mouse Schwann cells; and (iii) clonal rat Schwannoma RN22 cells. In chick sympathetic and mouse dorsal root ganglionic cultures, all 3 CMs supported survival of the same number of neurons as did mouse submaxillary NGF, and in most cases no increased survival resulted from concurrent administration of NGF and any one CM. NGF and CM activities were quantitated in each of the responsive cell systems. No differences were seen when either test population was used for the same agent, or when different CMs were examined on the same test cells. The CM activity, unlike that of NGF, was not blocked by even excess amounts of antiserum against mouse submaxillary NGF. The neuronotrophic activity of CMs appears to reside with macromolecular constituents. None of the CMs displayed trophic activity on chick embryo dorsal root ganglionic neurons. However, at least one of them (RN22 medium) had drastic effects on these ganglionic cells even in the presence of NGF, leaving open the possibility of a 'toxic' factor overriding putative trophic agents.
我们在此描述了利用3种已确立的神经生长因子(NGF)作用对象(来自解离的鸡胚交感神经节的培养神经元、鸡胚或新生小鼠背根神经节)来研究以下条件培养基(CMs)中的神经营养活性:(i)鸡胚心脏;(ii)纯化的小鼠雪旺细胞;以及(iii)克隆大鼠雪旺细胞瘤RN22细胞。在鸡胚交感神经和小鼠背根神经节培养物中,所有3种CMs支持存活的神经元数量与小鼠颌下NGF相同,并且在大多数情况下,同时给予NGF和任何一种CM并未导致存活增加。在每个反应性细胞系统中对NGF和CM活性进行了定量。当使用相同的试剂对任一测试群体进行检测,或者在相同的测试细胞上检测不同的CMs时,未观察到差异。与NGF不同,即使使用过量的抗小鼠颌下NGF抗血清也不能阻断CM活性。CMs的神经营养活性似乎存在于大分子成分中。没有一种CMs对鸡胚背根神经节神经元表现出营养活性。然而,它们中的至少一种(RN22培养基)即使在存在NGF的情况下对这些神经节细胞也有剧烈影响,这使得存在一种“毒性”因子凌驾于假定的营养因子之上的可能性。