Daniels M P
J Cell Biol. 1972 Apr;53(1):164-76. doi: 10.1083/jcb.53.1.164.
Inhibition of nerve fiber (neurite) formation by colchicine and Colcemid was studied in monolayer cultures of dissociated spinal ganglia of the chick. Replica cultures were fixed after appropriate incubation and alkaloid treatment. Quantitative estimates of the mean total neurite length per neuron (MNL) were made by use of camera lucida tracing. MNL values plotted against time of incubation gave control curves with an initial lag period, a phase of rapid increase, and a final phase in which MNL increase was retarded. Colchicine at 0.01-0.05 microg/ml (2.4 x 10(-8)-1.2 x 10(-7)M) caused reversible, concentration dependent, inhibition of the increase in MNL when applied during the lag period or phase of rapid increase. At the highest concentration there was a net decrease in MNL. The effect of Colcemid at 0.05 microg/ml was similar to that of colchicine, but more rapidly reversible. In most experiments there was no loss of neurons during the period of inhibition of MNL increase by colchicine or Colcemid. Therefore selective destruction of neurons was not involved in the inhibition of neurite growth. Prolonged incubation after treatment with the highest concentration used resulted in a 50% loss of neurons, in part through detachment of viable cells. Quantitative radioautography of the alkaloid-treated neurons with leucine-(14)C indicated little or no inhibition of incorporation into protein during inhibition of MNL increase. The results strongly suggest that inhibition of neurite growth involves a specific effect of colchicine, presumably the disruption of microtubules. They are thus consistent with the hypothesis that the polymerization of microtubules is essential to the formation of nerve fibers.
在鸡的离体脊髓神经节单层培养物中,研究了秋水仙碱和秋水仙酰胺对神经纤维(神经突)形成的抑制作用。在适当的孵育和生物碱处理后,对复制培养物进行固定。使用明视野显微镜追踪法对每个神经元的平均总神经突长度(MNL)进行定量估计。将MNL值与孵育时间作图,得到的对照曲线具有初始延迟期、快速增加期和最终MNL增加受阻的阶段。在延迟期或快速增加期施加浓度为0.01 - 0.05微克/毫升(2.4×10⁻⁸ - 1.2×10⁻⁷摩尔/升)的秋水仙碱会导致MNL增加的可逆性、浓度依赖性抑制。在最高浓度时,MNL出现净减少。浓度为0.05微克/毫升的秋水仙酰胺的作用与秋水仙碱相似,但可逆性更快。在大多数实验中,在秋水仙碱或秋水仙酰胺抑制MNL增加的期间,没有神经元丢失。因此,神经突生长的抑制不涉及神经元的选择性破坏。用所用最高浓度处理后延长孵育导致50%的神经元丢失,部分原因是活细胞的脱离。用亮氨酸 - ¹⁴C对生物碱处理的神经元进行定量放射自显影表明,在抑制MNL增加期间,蛋白质掺入几乎没有或没有受到抑制。结果强烈表明,神经突生长的抑制涉及秋水仙碱的特定作用,推测是微管的破坏。因此,它们与微管聚合对神经纤维形成至关重要的假设一致。