Grande Giovanbattista, Bui Tuan V, Rose P Ken
Canadian Institute for Health Research Group in Sensory-Motor Systems, Department of Physiology, Centre for Neuroscience Studies, Queen's University, Kingston, Ontario, Canada.
J Neurophysiol. 2007 Jun;97(6):4023-35. doi: 10.1152/jn.00044.2007. Epub 2007 Apr 11.
In the presence of monoamines, L-type Ca(2+) channels on the dendrites of motoneurons contribute to persistent inward currents (PICs) that can amplify synaptic inputs two- to sixfold. However, the exact location of the L-type Ca(2+) channels is controversial, and the importance of the location as a means of regulating the input-output properties of motoneurons is unknown. In this study, we used a computational strategy developed previously to estimate the dendritic location of the L-type Ca(2+) channels and test the hypothesis that the location of L-type Ca(2+) channels varies as a function of motoneuron size. Compartmental models were constructed based on dendritic trees of five motoneurons that ranged in size from small to large. These models were constrained by known differences in PIC activation reported for low- and high-conductance motoneurons and the relationship between somatic PIC threshold and the presence or absence of tonic excitatory or inhibitory synaptic activity. Our simulations suggest that L-type Ca(2+) channels are concentrated in hotspots whose distance from the soma increases with the size of the dendritic tree. Moving the hotspots away from these sites (e.g., using the hotspot locations from large motoneurons on intermediate-sized motoneurons) fails to replicate the shifts in PIC threshold that occur experimentally during tonic excitatory or inhibitory synaptic activity. In models equipped with a size-dependent distribution of L-type Ca(2+) channels, the amplification of synaptic current by PICs depends on motoneuron size and the location of the synaptic input on the dendritic tree.
在单胺存在的情况下,运动神经元树突上的L型Ca(2+)通道会产生持续内向电流(PICs),这种电流可将突触输入放大两到六倍。然而,L型Ca(2+)通道的确切位置存在争议,并且其位置作为调节运动神经元输入-输出特性的一种方式的重要性尚不清楚。在本研究中,我们使用先前开发的一种计算策略来估计L型Ca(2+)通道的树突位置,并检验L型Ca(2+)通道的位置随运动神经元大小而变化的假设。基于五个大小从小到的运动神经元的树突构建了房室模型。这些模型受到低电导和高电导运动神经元报告的PIC激活的已知差异以及体细胞PIC阈值与强直性兴奋性或抑制性突触活动的存在与否之间关系的约束。我们的模拟表明,L型Ca(2+)通道集中在热点区域,这些热点区域与胞体的距离随着树突树的大小而增加。将热点区域从这些位置移开(例如,在中等大小的运动神经元上使用大运动神经元的热点位置)无法复制在强直性兴奋性或抑制性突触活动期间实验中出现的PIC阈值变化。在配备有与大小相关的L型Ca(2+)通道分布的模型中,PIC对突触电流的放大取决于运动神经元的大小以及突触输入在树突树上的位置。