Khateeb Karam, Griggs Devon J, Sabes Philip N, Yazdan-Shahmorad Azadeh
Departments of Bioengineering, University of Washington; Washington National Primate Research Center.
Washington National Primate Research Center; Department of Electrical and Computer Engineering, University of Washington.
J Vis Exp. 2019 May 23(147). doi: 10.3791/59232.
In non-human primate (NHP) optogenetics, infecting large cortical areas with viral vectors is often a difficult and time-consuming task. Here, we demonstrate the use of magnetic resonance (MR)-guided convection enhanced delivery (CED) of optogenetic viral vectors into primary somatosensory (S1) and motor (M1) cortices of macaques to obtain efficient, widespread cortical expression of light-sensitive ion channels. Adeno-associated viral (AAV) vectors encoding the red-shifted opsin C1V1 fused to yellow fluorescent protein (EYFP) were injected into the cortex of rhesus macaques under MR-guided CED. Three months post-infusion, epifluorescent imaging confirmed large regions of optogenetic expression (>130 mm) in M1 and S1 in two macaques. Furthermore, we were able to record reliable light-evoked electrophysiology responses from the expressing areas using micro-electrocorticographic arrays. Later histological analysis and immunostaining against the reporter revealed widespread and dense optogenetic expression in M1 and S1 corresponding to the distribution indicated by epifluorescent imaging. This technique enables us to obtain expression across large areas of the cortex within a shorter period of time with minimal damage compared to the traditional techniques and can be an optimal approach for optogenetic viral delivery in large animals such as NHPs. This approach demonstrates great potential for network-level manipulation of neural circuits with cell-type specificity in animal models evolutionarily close to humans.
在非人灵长类动物(NHP)光遗传学研究中,使用病毒载体感染大面积皮质区域通常是一项困难且耗时的任务。在此,我们展示了在磁共振(MR)引导下,通过对流增强递送(CED)将光遗传学病毒载体注入猕猴的初级体感(S1)和运动(M1)皮质,以实现光敏感离子通道在皮质的高效、广泛表达。将编码与黄色荧光蛋白(EYFP)融合的红移视蛋白C1V1的腺相关病毒(AAV)载体在MR引导的CED下注入恒河猴的皮质。注入三个月后,落射荧光成像证实了两只猕猴的M1和S1区域存在大面积的光遗传学表达(>130平方毫米)。此外,我们能够使用微皮质电图阵列从表达区域记录可靠的光诱发电生理反应。随后的组织学分析和针对报告基因的免疫染色显示,M1和S1区域存在广泛且密集的光遗传学表达,与落射荧光成像所示的分布一致。与传统技术相比,该技术能够在更短的时间内,以最小的损伤在大面积皮质区域实现表达,并且可能是在诸如NHP等大型动物中进行光遗传学病毒递送的最佳方法。这种方法在进化上与人类接近的动物模型中,对于具有细胞类型特异性的神经回路进行网络水平的操纵具有巨大潜力。