Bayasgalan T, Stupniki S, Kovács A, Csemer A, Szentesi P, Pocsai K, Dionisio L, Spitzmaul G, Pál B
Department of Physiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Instituto de Investigaciones Bioquímicas de Bahía Blanca (INIBIBB), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Universidad Nacional Del Sur (UNS), Bahía Blanca, Argentina.
Front Cell Neurosci. 2021 Jul 26;15:707789. doi: 10.3389/fncel.2021.707789. eCollection 2021.
The pedunculopontine nucleus (PPN), a structure known as a cholinergic member of the reticular activating system (RAS), is source and target of cholinergic neuromodulation and contributes to the regulation of the sleep-wakefulness cycle. The M-current is a voltage-gated potassium current modulated mainly by cholinergic signaling. KCNQ subunits ensemble into ion channels responsible for the M-current. In the central nervous system, KCNQ4 expression is restricted to certain brainstem structures such as the RAS nuclei. Here, we investigated the presence and functional significance of KCNQ4 in the PPN by behavioral studies and the gene and protein expressions and slice electrophysiology using a mouse model lacking KCNQ4 expression. We found that this mouse has alterations in the adaptation to changes in light-darkness cycles, representing the potential role of KCNQ4 in the regulation of the sleep-wakefulness cycle. As cholinergic neurons from the PPN participate in the regulation of this cycle, we investigated whether the cholinergic PPN might also possess functional KCNQ4 subunits. Although the M-current is an electrophysiological hallmark of cholinergic neurons, only a subpopulation of them had KCNQ4-dependent M-current. Interestingly, the absence of the KCNQ4 subunit altered the expression patterns of the other KCNQ subunits in the PPN. We also determined that, in wild-type animals, the cholinergic inputs of the PPN modulated the M-current, and these in turn can modulate the level of synchronization between neighboring PPN neurons. Taken together, the KCNQ4 subunit is present in a subpopulation of PPN cholinergic neurons, and it may contribute to the regulation of the sleep-wakefulness cycle.
脚桥核(PPN)是网状激活系统(RAS)中已知的胆碱能结构成员,是胆碱能神经调节的来源和靶点,有助于调节睡眠-觉醒周期。M电流是一种主要由胆碱能信号调制的电压门控钾电流。KCNQ亚基组装成负责M电流的离子通道。在中枢神经系统中,KCNQ4的表达仅限于某些脑干结构,如RAS核。在这里,我们通过行为学研究、基因和蛋白质表达以及使用缺乏KCNQ4表达的小鼠模型进行切片电生理学研究,来探究KCNQ4在PPN中的存在及其功能意义。我们发现,这种小鼠在适应明暗周期变化方面存在改变,这表明KCNQ4在调节睡眠-觉醒周期中具有潜在作用。由于来自PPN的胆碱能神经元参与了这个周期的调节,我们研究了胆碱能PPN是否也可能拥有功能性的KCNQ4亚基。虽然M电流是胆碱能神经元的电生理标志,但只有其中一部分亚群具有KCNQ4依赖性M电流。有趣的是,KCNQ4亚基的缺失改变了PPN中其他KCNQ亚基的表达模式。我们还确定,在野生型动物中,PPN的胆碱能输入调节了M电流,而这些反过来又可以调节相邻PPN神经元之间的同步水平。综上所述,KCNQ4亚基存在于PPN胆碱能神经元的一个亚群中,并且可能有助于调节睡眠-觉醒周期。