Komatsu Misako, Sugano Eriko, Tomita Hiroshi, Fujii Naotaka
Ichinohe Group, Laboratory for Molecular Analysis of Higher Brain Function, RIKEN Brain Science InstituteSaitama, Japan.
Department of Chemistry and Biological Sciences, Iwate UniversityIwate, Japan.
Front Neurosci. 2017 Sep 15;11:514. doi: 10.3389/fnins.2017.00514. eCollection 2017.
Optogenetics has potential applications in the study of epilepsy and neuroprostheses, and for studies on neural circuit dynamics. However, to achieve translation to clinical usage, optogenetic interfaces that are capable of chronic stimulation and monitoring with minimal brain trauma are required. We aimed to develop a chronically implantable device for photostimulation of the brain of non-human primates. We used a micro-light-emitting diode (LED) array with a flexible polyimide film. The array was combined with a whole-cortex electrocorticographic (ECoG) electrode array for simultaneous photostimulation and recording. Channelrhodopsin-2 (ChR2) was virally transduced into the cerebral cortex of common marmosets, and then the device was epidurally implanted into their brains. We recorded the neural activity during photostimulation of the awake monkeys for 4 months. The neural responses gradually increased after the virus injection for ~8 weeks and remained constant for another 8 weeks. The micro-LED and ECoG arrays allowed semi-invasive simultaneous stimulation and recording during long-term implantation in the brains of non-human primates. The development of this device represents substantial progress in the field of optogenetic applications.
光遗传学在癫痫和神经假体研究以及神经回路动力学研究中具有潜在应用价值。然而,要实现向临床应用的转化,就需要能够在对大脑造成最小创伤的情况下进行长期刺激和监测的光遗传学接口。我们旨在开发一种可长期植入的装置,用于对非人类灵长类动物的大脑进行光刺激。我们使用了带有柔性聚酰亚胺薄膜的微型发光二极管(LED)阵列。该阵列与全皮质脑电描记(ECoG)电极阵列相结合,用于同时进行光刺激和记录。将通道视紫红质-2(ChR2)通过病毒转导到普通狨猴的大脑皮层中,然后将该装置硬膜外植入它们的大脑。我们记录了清醒猴子在光刺激期间4个月的神经活动。病毒注射后约8周,神经反应逐渐增强,并在接下来的8周内保持稳定。微型LED和ECoG阵列允许在长期植入非人类灵长类动物大脑期间进行半侵入性的同时刺激和记录。该装置的开发代表了光遗传学应用领域的重大进展。