Eichler M E, Rich K M
Department of Neurological Surgery, Washington University School of Medicine, St. Louis, MO 63110.
Brain Res. 1989 Mar 20;482(2):340-6. doi: 10.1016/0006-8993(89)91197-9.
The time course of dependence on nerve growth factor (NGF) for survival in sensory neurons in vitro was examined with microscopic and biochemical methods. Primary dorsal root ganglion (DRG) cultures from embryonic-day-15 (E-15) and day-19 (E-19) rats were maintained with standard dissociated cell culture techniques in the absence of most non-neuronal cells. After various times in culture, neurons were acutely deprived of neurotrophic support by changing to NGF-free medium and adding NGF antiserum to eliminate any residual NGF. Neuronal cultures were examined with phase microscopy; and, their metabolic activity was measured with a protein assay at various time points after NGF deprivation. E-15 neurons grown in culture for 5 days were exquisitely sensitive to acute NGF deprivation. By 12 h after NGF deprivation, neuronal morphology was severely disrupted and the majority of neurons appeared dead. E-15 neurons grown in culture for 8 or 11 days showed progressively less dependence on NGF for survival. These older neurons did not die until 24 and 48 h, respectively, following NGF withdrawal. Neurons grown in culture for 20 days did not show any morphologic changes by phase microscopy up to 4 days after NGF deprivation. Protein incorporation progressively decreased between 12 and 48 h after NGF withdrawal in E-15 neurons grown in culture for 5, 8, or 11 days.(ABSTRACT TRUNCATED AT 250 WORDS)
运用显微镜和生化方法研究了体外培养的感觉神经元对神经生长因子(NGF)的存活依赖时间进程。采用标准的解离细胞培养技术,在无大多数非神经元细胞的条件下,培养来自胚胎第15天(E-15)和第19天(E-19)大鼠的初级背根神经节(DRG)。培养不同时间后,通过更换为无NGF培养基并添加NGF抗血清以消除任何残留的NGF,使神经元急性缺乏神经营养支持。用相差显微镜检查神经元培养物;并在剥夺NGF后的不同时间点,通过蛋白质测定法测量其代谢活性。体外培养5天的E-15神经元对急性NGF剥夺极为敏感。在剥夺NGF后12小时,神经元形态严重破坏,大多数神经元似乎死亡。体外培养8天或11天的E-15神经元对NGF存活的依赖性逐渐降低。这些较老的神经元在撤除NGF后分别直到24小时和48小时才死亡。体外培养20天的神经元在剥夺NGF后长达4天,相差显微镜下未显示任何形态学变化。在体外培养5天、8天或11天的E-15神经元中,蛋白质掺入在撤除NGF后12至48小时逐渐减少。(摘要截断于250字)