Romer Shannon H, Deardorff Adam S, Fyffe Robert E W
Department of Neuroscience, Cell Biology and Physiology, Boonshoft School of Medicine, Wright State University, Dayton, Ohio.
Department of Neuroscience, Cell Biology and Physiology, Boonshoft School of Medicine, Wright State University, Dayton, Ohio
Physiol Rep. 2016 Nov;4(22). doi: 10.14814/phy2.13039.
Homeostatic plasticity occurs through diverse cellular and synaptic mechanisms, and extensive investigations over the preceding decade have established Kv2.1 ion channels as key homeostatic regulatory elements in several central neuronal systems. As in these cellular systems, Kv2.1 channels in spinal motoneurons (MNs) localize within large somatic membrane clusters. However, their role in regulating motoneuron activity is not fully established in vivo. We have previously demonstrated marked Kv2.1 channel redistribution in MNs following in vitro glutamate application and in vivo peripheral nerve injury (Romer et al., 2014, Brain Research, 1547:1-15). Here, we extend these findings through the novel use of a fully intact, in vivo rat preparation to show that Kv2.1 ion channels in lumbar MNs rapidly and reversibly redistribute throughout the somatic membrane following 10 min of electrophysiological sensory and/or motor nerve stimulation. These data establish that Kv2.1 channels are remarkably responsive in vivo to electrically evoked and synaptically driven action potentials in MNs, and strongly implicate motoneuron Kv2.1 channels in the rapid homeostatic response to altered neuronal activity.
稳态可塑性通过多种细胞和突触机制发生,在过去十年中,广泛的研究已将Kv2.1离子通道确立为几个中枢神经系统中的关键稳态调节元件。与这些细胞系统一样,脊髓运动神经元(MNs)中的Kv2.1通道定位于大型体细胞膜簇内。然而,它们在调节运动神经元活动中的作用在体内尚未完全明确。我们之前已经证明,在体外应用谷氨酸和体内周围神经损伤后,MNs中Kv2.1通道会发生显著的重新分布(Romer等人,2014年,《脑研究》,1547:1-15)。在这里,我们通过全新使用完全完整的体内大鼠制备方法扩展了这些发现,以表明在电生理感觉和/或运动神经刺激10分钟后,腰段MNs中的Kv2.1离子通道会在整个体细胞膜上迅速且可逆地重新分布。这些数据表明,Kv2.1通道在体内对MNs中电诱发和突触驱动的动作电位具有显著反应,并强烈表明运动神经元Kv2.1通道参与了对神经元活动改变的快速稳态反应。