Han Xue, Qian Xiaofeng, Bernstein Jacob G, Zhou Hui-Hui, Franzesi Giovanni Talei, Stern Patrick, Bronson Roderick T, Graybiel Ann M, Desimone Robert, Boyden Edward S
Media Lab, Synthetic Neurobiology Group, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA.
Neuron. 2009 Apr 30;62(2):191-8. doi: 10.1016/j.neuron.2009.03.011.
To understand how brain states and behaviors are generated by neural circuits, it would be useful to be able to perturb precisely the activity of specific cell types and pathways in the nonhuman primate nervous system. We used lentivirus to target the light-activated cation channel channelrhodopsin-2 (ChR2) specifically to excitatory neurons of the macaque frontal cortex. Using a laser-coupled optical fiber in conjunction with a recording microelectrode, we showed that activation of excitatory neurons resulted in well-timed excitatory and suppressive influences on neocortical neural networks. ChR2 was safely expressed, and could mediate optical neuromodulation, in primate neocortex over many months. These findings highlight a methodology for investigating the causal role of specific cell types in nonhuman primate neural computation, cognition, and behavior, and open up the possibility of a new generation of ultraprecise neurological and psychiatric therapeutics via cell-type-specific optical neural control prosthetics.
为了理解神经回路如何产生脑状态和行为,能够精确干扰非人类灵长类动物神经系统中特定细胞类型和神经通路的活动将是很有用的。我们使用慢病毒将光激活阳离子通道视紫红质-2(ChR2)特异性靶向猕猴额叶皮质的兴奋性神经元。结合记录微电极使用激光耦合光纤,我们表明兴奋性神经元的激活对新皮质神经网络产生了适时的兴奋和抑制作用。ChR2在灵长类新皮质中安全表达,并能介导光学神经调节作用长达数月之久。这些发现突出了一种用于研究特定细胞类型在非人类灵长类动物神经计算、认知和行为中的因果作用的方法,并通过细胞类型特异性光学神经控制假体开辟了新一代超精确神经和精神治疗方法的可能性。