Brenneman D E, Fitzgerald S, Nelson P G
Brain Res. 1984 Aug;317(2):211-7. doi: 10.1016/0165-3806(84)90098-1.
The effect of conditioned medium (CM) on tetrodotoxin (TTX)-mediated neuronal cell death was investigated in dissociated spinal cord-dorsal root ganglion (SC-DRG) cultures. Nutrient medium was collected from donor SC-DRG cultures at 3--4-day intervals throughout development. The presence of survival-promoting neurotrophic material (NTM) in the conditioned medium was tested on TTX-treated cultures which were within the critical period of vulnerability to electrical blockade (days 7-21 in culture). Cultures were assayed by neuronal cell counts, choline acetyltransferase (ChAT) activity or fixation of [125I]tetanus toxin, a neuronal surface marker. Evidence of NTM was found in CM collected prior to day 8 and after day 21 in culture. Increasing the percentage of CM in fresh nutrient medium resulted in a dose-dependent increase in [125I]tetanus toxin fixation and ChAT activity in TTX-treated cultures. In addition, CM plus TTX treatment produced a 25% increase in neuronal cell counts as compared to controls. TTX treatment alone resulted in 20-25% decrease in neuronal number from that of control cultures. Cultures treated with CM alone had neuronal counts that were similar to controls. When electrical activity was blocked with TTX, NTM was not detectable in CM collected from donor cells during days 1-5. CM obtained from control cultures during the same interval had NTM activity. The existence of the critical period for electrical blockade-associated neuron death is associated with a decrease in the availability of NTM. Furthermore, the release of NTM from donor cells and the survival response of target neurons to NTM are apparently dependent on ongoing electrical activity.
在解离的脊髓 - 背根神经节(SC - DRG)培养物中研究了条件培养基(CM)对河豚毒素(TTX)介导的神经元细胞死亡的影响。在整个发育过程中,每隔3 - 4天从供体SC - DRG培养物中收集营养培养基。在处于对电传导阻滞敏感的关键时期(培养7 - 21天)的TTX处理的培养物上测试条件培养基中促存活神经营养物质(NTM)的存在。通过神经元细胞计数、胆碱乙酰转移酶(ChAT)活性或神经元表面标志物[125I]破伤风毒素的结合来检测培养物。在培养第8天之前和第21天之后收集的CM中发现了NTM的证据。在新鲜营养培养基中增加CM的百分比导致TTX处理的培养物中[125I]破伤风毒素结合和ChAT活性呈剂量依赖性增加。此外,与对照组相比,CM加TTX处理使神经元细胞计数增加了25%。单独TTX处理导致神经元数量比对照培养物减少20 - 25%。单独用CM处理的培养物的神经元计数与对照相似。当用TTX阻断电活动时,在第1 - 5天从供体细胞收集的CM中未检测到NTM。在相同时间段从对照培养物获得的CM具有NTM活性。与电传导阻滞相关的神经元死亡关键时期的存在与NTM可用性的降低有关。此外,NTM从供体细胞的释放以及靶神经元对NTM的存活反应显然依赖于持续的电活动。