Muennich Elizabeth A L, Fyffe R E W
Department of Anatomy and Physiology, Wright State University, Dayton, OH 45435, USA.
J Physiol. 2004 Feb 1;554(Pt 3):673-85. doi: 10.1113/jphysiol.2003.056192. Epub 2003 Nov 7.
Delayed rectifier K+ currents are involved in the control of alpha-motoneurone excitability, but the precise spatial distribution and organization of the membrane ion channels that contribute to these currents have not been defined. Voltage-activated Kv2.1 channels have properties commensurate with a contribution to delayed rectifier currents and are expressed in neurones throughout the mammalian central nervous system. A specific antibody against Kv2.1 channel subunits was used to determine the surface distribution and clustering of Kv2.1 subunit-containing channels in the cell membrane of alpha-motoneurones and other spinal cord neurones. In alpha-motoneurones, Kv2.1 immunoreactivity (-IR) was abundant in the surface membrane of the soma and large proximal dendrites, and was present also in smaller diameter distal dendrites. Plasma membrane-associated Kv2.1-IR in alpha-motoneurones was distributed in a mosaic of small irregularly shaped, and large disc-like, clusters. However, only small to medium clusters of Kv2.1-IR were observed in spinal interneurones and projection neurones, and some interneurones, including Renshaw cells, lacked demonstrable Kv2.1-IR. In alpha-motoneurones, dual immunostaining procedures revealed that the prominent disc-like domains of Kv2.1-IR are invariably apposed to presynaptic cholinergic C-terminals. Further, Kv2.1-IR colocalizes with immunoreactivity against postsynaptic muscarinic (m2) receptors at these locations. Ultrastructural examination confirmed the postsynaptic localization of Kv2.1-IR at C-terminal synapses, and revealed clusters of Kv2.1-IR at a majority of S-type, presumed excitatory, synapses. Kv2.1-IR in alpha-motoneurones is not directly associated with presumed inhibitory (F-type) synapses, nor is it present in presynaptic structures apposed to the motoneurone. Occasionally, small patches of extrasynaptic Kv2.1-IR labelling were observed in surface membrane apposed by glial processes. Voltage-gated potassium channels responsible for the delayed rectifier current, including Kv2.1, are usually assigned roles in the repolarization of the action potential. However, the strategic localization of Kv2.1 subunit-containing channels at specific postsynaptic sites suggests that this family of voltage-activated K+ channels may have additional roles and/or regulatory components.
延迟整流钾电流参与α运动神经元兴奋性的调控,但对这些电流有贡献的膜离子通道的精确空间分布和组织尚未明确。电压门控的Kv2.1通道具有与延迟整流电流贡献相匹配的特性,并且在整个哺乳动物中枢神经系统的神经元中均有表达。使用针对Kv2.1通道亚基的特异性抗体来确定α运动神经元和其他脊髓神经元细胞膜中含Kv2.1亚基通道的表面分布和聚集情况。在α运动神经元中,Kv2.1免疫反应性(-IR)在胞体和大的近端树突的表面膜中丰富,并且在较小直径的远端树突中也存在。α运动神经元中与质膜相关的Kv2.1-IR分布在小的不规则形状和大的盘状簇的镶嵌结构中。然而,在脊髓中间神经元和投射神经元中仅观察到小到中等大小的Kv2.1-IR簇,并且一些中间神经元,包括闰绍细胞,缺乏可检测到的Kv2.1-IR。在α运动神经元中,双重免疫染色程序显示Kv2.1-IR的突出盘状结构域总是与突触前胆碱能C末端相邻。此外,在这些位置,Kv2.1-IR与针对突触后毒蕈碱(m2)受体的免疫反应性共定位。超微结构检查证实了Kv2.1-IR在C末端突触处的突触后定位,并在大多数假定为兴奋性的S型突触处发现了Kv2.1-IR簇。α运动神经元中的Kv2.1-IR不直接与假定的抑制性(F型)突触相关,也不存在于与运动神经元相邻的突触前结构中。偶尔,在被胶质细胞突起覆盖的表面膜中观察到小的突触外Kv2.1-IR标记斑块。负责延迟整流电流的电压门控钾通道,包括Kv2.1,通常在动作电位的复极化中起作用。然而,含Kv2.1亚基通道在特定突触后位点的战略定位表明,这个电压门控钾通道家族可能具有额外的作用和/或调节成分。