Johnson B D, Byerly L
Department of Biological Sciences, University of Southern California, Los Angeles 90089-2520.
Pflugers Arch. 1994 Nov;429(1):14-21. doi: 10.1007/BF02584025.
Ca2+ channel inactivation was investigated in acutely isolated hippocampal pyramidal neurons from adult rats and found to have a component dependent on intracellular Ca2+. Ca(2+)-dependent inactivation was indentified as the additional inactivation of channel current observed when Ca2+ replaced Ba2+ as the current carrying ion, and was found to be an independent process from that of Ba2+ current inactivation based on three lines of evidence: (1) no correlation between Ca(2+)-dependent inactivation and Ba2+ current inactivation was found, (2) only Ca(2+)-dependent inactivation was reduced by intracellular application of Ca2+ chelators, and (3) only Ca(2+)-dependent inactivation was sensitive to compounds which alter the cytoskeleton. Drugs which stabilize (taxol and phalloidin) and destabilize (colchicine and cytochalasin B) the cytoskeleton altered the development and recovery from Ca(2+)-dependent inactivation, indicating that the neuronal cytoskeleton may mediate Ca2+ channel sensitivity to intracellular Ca2+. Ca(2+)-dependent inactivation was not associated with a particular subset of Ca2+ channels, suggesting that all Ca2+ channels in these neurons are inactivated by intracellular Ca2+.
在成年大鼠急性分离的海马锥体神经元中研究了Ca2+通道失活,发现其具有依赖于细胞内Ca2+的成分。Ca(2+)依赖性失活被确定为当Ca2+取代Ba2+作为载流离子时观察到的通道电流的额外失活,并且基于三条证据发现其是一个与Ba2+电流失活独立的过程:(1) 未发现Ca(2+)依赖性失活与Ba2+电流失活之间存在相关性,(2) 细胞内应用Ca2+螯合剂仅降低了Ca(2+)依赖性失活,(3) 仅Ca(2+)依赖性失活对改变细胞骨架的化合物敏感。稳定(紫杉醇和鬼笔环肽)和破坏(秋水仙碱和细胞松弛素B)细胞骨架的药物改变了Ca(2+)依赖性失活的发展和恢复,表明神经元细胞骨架可能介导Ca2+通道对细胞内Ca2+的敏感性。Ca(2+)依赖性失活与特定的Ca(2+)通道亚群无关,这表明这些神经元中的所有Ca2+通道都被细胞内Ca2+失活。