Shimba Kenta, Kotani Kiyoshi, Jimbo Yasuhiko
IEEE Trans Biomed Eng. 2021 Dec;68(12):3574-3581. doi: 10.1109/TBME.2021.3078473. Epub 2021 Nov 19.
Neuronal networks are fundamental structures for information processing in the central nervous system. This processing function is severely impaired by abnormal axonal conduction from changes in functional ion channel expression. The evaluation of axonal conduction properties can be effective in the early diagnosis of information-processing abnormalities. However, little is known about functional ion channel expression in axons owing to lack of an appropriate method. In this study, we developed a device to measure changes in axonal conduction properties by selective pharmacological stimulation for the functional evaluation of Na channels expressed in axons.
Axons of rat cortical neurons were guided across a pair of electrodes through microtunnel structures by employing surface patterning.
The developed device detected more than 50 axons while recording for 10 min. The conduction delay along the axons decreased by 22.5% with neuron maturation. Tetrodotoxin and lidocaine (Na channel blockers) increased the conduction delay in a concentration-dependent manner depending on their working concentrations, indicating the effectiveness of the device. Finally, selective Na channel blockers for various Na channel subtypes were used. Phrixotoxin, a Nav1.2 blocker, markedly increased the conduction delay, suggesting that Nav1.2 is functionally expressed in the unmyelinated axons of the cerebral cortex.
These results show that our device is feasible for the high-throughput functional evaluation of Na channel subtypes in axons.
The results obtained can contribute to the understanding of the pathogenic mechanisms of neurological diseases that involve changes in the functional expression states of ion channels in axons.
神经网络是中枢神经系统中信息处理的基本结构。功能离子通道表达的变化导致轴突传导异常,严重损害了这种信息处理功能。评估轴突传导特性有助于早期诊断信息处理异常。然而,由于缺乏合适的方法,关于轴突中功能离子通道的表达知之甚少。在本研究中,我们开发了一种装置,通过选择性药理学刺激来测量轴突传导特性的变化,以对轴突中表达的钠通道进行功能评估。
采用表面图案化技术,引导大鼠皮质神经元的轴突穿过微隧道结构中的一对电极。
所开发的装置在记录10分钟时可检测到50多条轴突。随着神经元成熟,沿轴突的传导延迟降低了22.5%。河豚毒素和利多卡因(钠通道阻滞剂)根据其工作浓度以浓度依赖性方式增加传导延迟,表明该装置有效。最后,使用了针对各种钠通道亚型的选择性钠通道阻滞剂。Phrixotoxin,一种Nav1.2阻滞剂,显著增加了传导延迟,表明Nav1.2在大脑皮质的无髓鞘轴突中功能性表达。
这些结果表明,我们的装置对于轴突中钠通道亚型的高通量功能评估是可行的。
所获得的结果有助于理解涉及轴突中离子通道功能表达状态变化的神经疾病的致病机制。