Gomez T M, Snow D M, Letourneau P C
University of Minnesota, Department of Cell Biology and Neuroanatomy, Minneapolis 55455, USA.
Neuron. 1995 Jun;14(6):1233-46. doi: 10.1016/0896-6273(95)90270-8.
This study examines the mechanisms of spontaneous and induced [Ca2+]i spiking in nerve growth cones and the effect of spikes on growth cone migration. Over a 10-20 min observation period, 29% of DRG growth cones undergo spontaneous and transient elevations in physiological extracellular Ca2+ ((Ca2+)o; 2 mM), whereas 67% of growth cones exposed to 20 mM (Ca2+)o exhibit similar [Ca2+]i spikes. Spontaneous [Ca2+]i spiking was not observed in neuronal cell bodies or nonneuronal cells. Ca2+ influx through non-voltage-gated Ca2+ channels was required for spontaneous [Ca2+]i spikes in growth cones, since removal of (Ca2+)o, or addition of the general Ca2+ channel blockers La3+ or Ni2+, reversibly blocked [Ca2+]i spiking, while blockers of the voltage-gated Ca2+ channels did not. Experiments using agents that influence intracellular Ca2+ stores suggest that Ca2+ stores may buffer and release Ca2+ during growth cone [Ca2+]i spikes. Growth cone migration was immediately and transiently inhibited by [Ca2+]i spikes, but eventually returned to prespike rates.
本研究考察了神经生长锥中[Ca2+]i自发和诱发尖峰的机制以及尖峰对生长锥迁移的影响。在10 - 20分钟的观察期内,29%的背根神经节(DRG)生长锥在生理细胞外Ca2+浓度((Ca2+)o;2 mM)下经历自发和短暂的升高,而67%暴露于20 mM (Ca2+)o的生长锥表现出类似的[Ca2+]i尖峰。在神经元细胞体或非神经元细胞中未观察到自发的[Ca2+]i尖峰。生长锥中自发的[Ca2+]i尖峰需要通过非电压门控Ca2+通道的Ca2+内流,因为去除(Ca2+)o,或添加通用的Ca2+通道阻滞剂La3+或Ni2+,可可逆地阻断[Ca2+]i尖峰,而电压门控Ca2+通道阻滞剂则无此作用。使用影响细胞内Ca2+储存的试剂进行的实验表明,在生长锥[Ca2+]i尖峰期间,Ca2+储存可能缓冲并释放Ca2+。[Ca2+]i尖峰可立即并短暂抑制生长锥迁移,但最终会恢复到尖峰前的速率。