Lupinsky Derek A, Magoski Neil S
Department of Physiology, Queen's University, 4th Floor, Botterell Hall, 18 Stuart Street, Kingston, ON, Canada, K7L 3N6.
J Physiol. 2006 Sep 1;575(Pt 2):491-506. doi: 10.1113/jphysiol.2006.105833. Epub 2006 Jun 8.
Ca2+-activated, non-selective cation channels feature prominently in the regulation of neuronal excitability, yet the mechanism of their Ca2+ activation is poorly defined. In the bag cell neurones of Aplysia californica, opening of a voltage-gated, non-selective cation channel initiates a long-lasting afterdischarge that induces egg-laying behaviour. The present study used single-channel recording to investigate Ca2+ activation in this cation channel. Perfusion of Ca2+ onto the cytoplasmic face of channels in excised, inside-out patches yielded a Ca2+ activation EC50 of 10 microm with a Hill coefficient of 0.66. Increasing Ca2+ from 100 nm to 10 microm caused an apparent hyperpolarizing shift in the open probability (Po) versus voltage curve. Beyond 10 microm Ca2+, additional changes in voltage dependence were not evident. Perfusion of Ba2+ onto the cytoplasmic face did not alter Po; moreover, in outside-out recordings, Po was decreased by replacing external Ca2+ with Ba2+ as a charge carrier, suggesting Ca2+ influx through the channel may provide positive feedback. The lack of Ba2+ sensitivity implicated calmodulin in Ca2+ activation. Consistent with this, the application to the cytoplasmic face of calmodulin antagonists, calmidazolium and calmodulin-binding domain, reduced Po, whereas exogenous calmodulin increased Po. Overall, the data indicated that the cation channel is activated by Ca2+ through closely associated calmodulin. Bag cell neurone intracellular Ca2+ rises markedly at the onset of the afterdischarge, which would enhance channel opening and promote bursting to elicit reproduction. Cation channels are essential to nervous system function in many organisms, and closely associated calmodulin may represent a widespread mechanism for their Ca2+ sensitivity.
钙离子激活的非选择性阳离子通道在神经元兴奋性调节中起着重要作用,但其钙离子激活机制仍不清楚。在加州海兔的袋状细胞神经元中,电压门控非选择性阳离子通道的开放引发了一个持久的后放电,从而诱导产卵行为。本研究使用单通道记录来研究该阳离子通道中的钙离子激活情况。将钙离子灌注到切除的内面向外膜片中通道的胞质面,得到钙离子激活的半数有效浓度(EC50)为10微摩尔,希尔系数为0.66。将钙离子浓度从100纳米增加到10微摩尔,导致开放概率(Po)与电压曲线出现明显的超极化偏移。超过10微摩尔钙离子后,电压依赖性的其他变化不明显。将钡离子灌注到胞质面不会改变Po;此外,在外面向外记录中,用钡离子作为电荷载体替代外部钙离子会降低Po,这表明通过通道的钙离子内流可能提供正反馈。缺乏钡离子敏感性表明钙调蛋白参与了钙离子激活。与此一致的是,将钙调蛋白拮抗剂、氯米达唑和钙调蛋白结合结构域应用于胞质面会降低Po,而外源性钙调蛋白会增加Po。总体而言,数据表明阳离子通道通过紧密相关的钙调蛋白被钙离子激活。袋状细胞神经元的细胞内钙离子在放电开始时显著升高,这将增强通道开放并促进爆发以引发繁殖。阳离子通道对许多生物体的神经系统功能至关重要,紧密相关的钙调蛋白可能代表了它们对钙离子敏感性的一种广泛机制。