O'Lague P H, Huttner S L, Vandenberg C A, Morrison-Graham K, Horn R
J Neurosci Res. 1985;13(1-2):301-21. doi: 10.1002/jnr.490130120.
Large growth cones were produced in vitro by nerve growth factor (NGF) treatment of multinucleate cells produced by chemical fusion of cells of the neuron-like clone PC12. These endings were studied both at the light microscopic and ultrastructural levels. The activity of ionic channels at growth cones was recorded with intracellular microelectrodes, patch recording of single channels, and whole cone recording from mechanically isolated growth cones. Morphologically, these large growth cones were characterized by the presence of microspikes and filopodia, by the presence of actin demonstrated immunohistochemically, and by the presence of catecholamine fluorescence. At the ultrastructural level they contained a broad spectrum of organelles with a distribution characteristic of neuronal growth cones, including dense core vesicles, abundant smooth membrane cisternae, microtubules, and a filamentous network. The presence of channels capable of generating action potentials was revealed by intracellular microelectrode recording from the growth cone in the presence of locally applied tetraethylammonium (TEA). TEA appeared to block outward current channels that could effectively shunt inward current activated by depolarization. Action potentials elicited by depolarizing current in the presence of TEA could be blocked reversibly by Cd2+, a specific blocker of Ca channels. These action potentials were often followed by a long after-hyperpolarization lasting hundreds of milliseconds. This after-hyperpolarization was similar to that recorded in the cell body of PC12 cells where it appears to be mediated by Ca-activated K current. Single channel recording from outside-out excised patches of membrane from the growth cones perfused with KF revealed the presence of voltage sensitive Na channels, Ca-activated K channels, and K channels resembling delayed rectifier K channels. Macroscopic currents recorded from mechanically isolated growth cones in the "whole cone" configuration showed rapid inward currents at potentials greater than or equal to -40 mV, followed by delayed outward currents at more positive potentials, a finding providing additional evidence for the presence of Na and K channels in growth cones.
通过用神经生长因子(NGF)处理由类神经元克隆PC12细胞化学融合产生的多核细胞,在体外产生了大型生长锥。在光学显微镜和超微结构水平上对这些末梢进行了研究。用细胞内微电极、单通道膜片钳记录以及对机械分离的生长锥进行全锥记录来记录生长锥处离子通道的活性。在形态学上,这些大型生长锥的特征在于存在微棘和丝状伪足、免疫组织化学显示存在肌动蛋白以及存在儿茶酚胺荧光。在超微结构水平上,它们含有多种细胞器,其分布具有神经元生长锥的特征,包括致密核心囊泡、丰富的光滑膜池、微管和丝状网络。通过在局部应用四乙铵(TEA)的情况下从生长锥进行细胞内微电极记录,揭示了能够产生动作电位的通道的存在。TEA似乎阻断了外向电流通道,该通道可有效分流由去极化激活的内向电流。在存在TEA的情况下由去极化电流引发的动作电位可被Ca通道的特异性阻断剂Cd2+可逆地阻断。这些动作电位之后常常跟随持续数百毫秒的长时间超极化后电位。这种超极化后电位类似于在PC12细胞胞体中记录到的,在那里它似乎由Ca激活的K电流介导。从用KF灌注的生长锥的外向膜片上进行单通道记录,揭示了电压敏感Na通道、Ca激活K通道以及类似于延迟整流K通道的K通道的存在。从处于“全锥”配置的机械分离的生长锥记录的宏观电流显示,在电位大于或等于-40 mV时出现快速内向电流,随后在更正的电位出现延迟外向电流,这一发现为生长锥中存在Na和K通道提供了额外证据。