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Swimming Against the Tide: Investigations of the C-Bouton Synapse

机译:逆潮流而行:C-布顿突触的调查

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摘要

C-boutons are important cholinergic modulatory loci for state-dependent alterations in motoneuron firing rate. m2 receptors are concentrated postsynaptic to C-boutons, and m2 receptor activation increases motoneuron excitability by reducing the action potential afterhyperpolarization. Here, using an intensive review of the current literature as well as data from our laboratory, we illustrate that C-bouton postsynaptic sites comprise a unique structural/functional domain containing appropriate cellular machinery (a “signaling ensemble”) for cholinergic regulation of outward K+ currents. Moreover, synaptic reorganization at these critical sites has been observed in a variety of pathologic states. Yet despite recent advances, there are still great challenges for understanding the role of C-bouton regulation and dysregulation in human health and disease. The development of new therapeutic interventions for devastating neurological conditions will rely on a complete understanding of the molecular mechanisms that underlie these complex synapses. Therefore, to close this review, we propose a comprehensive hypothetical mechanism for the cholinergic modification of α-MN excitability at C-bouton synapses, based on findings in several well-characterized neuronal systems.
机译:C-boutons是重要的胆碱能调节基因座,用于运动神经元放电速率的状态依赖性改变。 m2受体集中在突触后到C-钮扣,并且m2受体的激活通过降低超极化后的动作电位来增加运动神经元的兴奋性。在这里,通过对当前文献以及我们实验室的数据进行的深入回顾,我们证明了C-bouton突触后位点包含一个独特的结构/功能域,该域包含适当的细胞机制(“信号合奏”),用于向外K +的胆碱能调节。潮流。此外,已经在各种病理状态下观察到了这些关键部位的突触重组。尽管有最新进展,但要理解C-bouton调节和失调在人类健康和疾病中的作用仍面临巨大挑战。用于破坏性神经系统疾病的新治疗干预措施的开发将取决于对这些复杂突触基础的分子机制的完整理解。因此,为结束本综述,我们基于一些功能完备的神经元系统的发现,提出了一种全面的假设机制,用于在C-bouton突触中胆碱能修饰α-MN的兴奋性。

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