Vollum Institute, Oregon Health and Science University, Portland, OR, 97239, USA.
Department of Behavioral Neuroscience, Oregon Health and Science University, Portland, OR, 97239, USA.
Nat Commun. 2021 Nov 19;12(1):6762. doi: 10.1038/s41467-021-26521-3.
The underlying mechanisms that promote precise spiking in upper motor neurons controlling fine motor skills are not well understood. Here we report that projection neurons in the adult zebra finch song nucleus RA display robust high-frequency firing, ultra-narrow spike waveforms, superfast Na current inactivation kinetics, and large resurgent Na currents (I). These properties of songbird pallial motor neurons closely resemble those of specialized large pyramidal neurons in mammalian primary motor cortex. They emerge during the early phases of song development in males, but not females, coinciding with a complete switch of Na+ channel subunit expression from Navβ3 to Navβ4. Dynamic clamping and dialysis of Navβ4's C-terminal peptide into juvenile RA neurons provide evidence that Navβ4, and its associated I, promote neuronal excitability. We thus propose that I modulates the excitability of upper motor neurons that are required for the execution of fine motor skills.
尚不清楚促进控制精细运动的上运动神经元精确放电的潜在机制。在这里,我们报告说,成年斑马雀鸣禽 RA 核中的投射神经元表现出强大的高频放电、超窄的尖峰波形、超快的 Na 电流失活动力学和大的再生 Na 电流(I)。鸣禽大脑皮层运动神经元的这些特性与哺乳动物初级运动皮层中专门的大型锥形神经元非常相似。它们出现在雄性而不是雌性的早期歌唱发育阶段,与 Navβ3 到 Navβ4 的 Na+通道亚单位表达完全转换同时发生。动态箝位和 Navβ4 的 C 末端肽在幼年 RA 神经元中的透析提供了证据,表明 Navβ4 及其相关的 I 促进神经元兴奋性。因此,我们提出 I 调节精细运动技能执行所需的上运动神经元的兴奋性。