Division of Neuropharmacology and Neurological Disorders, Yerkes National Primate Research Center, Emory University, Atlanta, GA, USA.
Udall Center of Excellence for Parkinson's Disease Research, Atlanta, GA, USA.
Eur J Neurosci. 2020 Dec;52(12):4824-4839. doi: 10.1111/ejn.15027. Epub 2020 Nov 11.
Retrogradely-transducing viral vectors are versatile tools for anatomical and functional interrogations of neural circuits. These vectors can be applied in nonhuman primates (NHPs), powerful model species for neuroscientific studies with limited genetic tractability, but limited data are available regarding the tropism and transgene expression patterns of such viruses after injections in NHP brains. Consequently, NHP researchers must often rely on related data available from other species for experimental planning. To evaluate the suitability of rAAV2-retro in the NHP basal ganglia, we studied the transgene expression patterns at the light and electron microscope level after injections of rAAV2-retro vector encoding the opsin Jaws conjugated to a green fluorescent protein (GFP) in the putamen of rhesus macaques. For inter-species comparison, we injected the same vector in the rat dorsal striatum. In both species, GFP expression was observed in numerous cortical and subcortical regions with known striatal projections. However, important inter-species differences in pathway transduction were seen, including labeling of the intralaminar thalamostriatal projection in rats, but not monkeys. Electron microscopic ultrastructural observations within the basal ganglia revealed GFP labeling in both postsynaptic dendrites and presynaptic axonal terminals; the latter likely derived from anterograde transgene transport in neurons that project to the striatum, and from collaterals of these neurons. Our results suggest that certain neural pathways may be refractory to transduction by retrograde vectors in a species-specific manner, highlighting the need for caution when determining the suitability of a retrograde vector for NHP studies based solely on rodent data.
逆行转导病毒载体是研究神经回路解剖结构和功能的多功能工具。这些载体可应用于非人类灵长类动物(NHPs),NHP 是神经科学研究中具有强大模型物种,但遗传可操作性有限,关于此类病毒在 NHP 大脑注射后的趋向性和转基因表达模式的数据有限。因此,NHP 研究人员在进行实验规划时,通常必须依赖其他物种的相关数据。为了评估 rAAV2-retro 在 NHP 基底神经节中的适用性,我们研究了 rAAV2-retro 载体(编码与绿色荧光蛋白(GFP)连接的 opsin Jaws)在恒河猴苍白球中的注射后,在光镜和电镜水平上的转基因表达模式。为了进行种间比较,我们在大鼠背侧纹状体中注射了相同的载体。在这两种物种中,GFP 表达都在具有已知纹状体投射的众多皮质和皮质下区域中观察到。然而,在种间通路转导方面存在重要差异,包括在大鼠中标记丘脑纹状体投射的内斑层,而在猴子中则没有。在基底神经节内的电子显微镜超微结构观察显示 GFP 标记在突触后树突和突触前轴突末端;后者可能源自投射到纹状体的神经元中的顺行转基因运输,以及这些神经元的侧支。我们的结果表明,某些神经通路可能以特定于物种的方式对逆行载体产生抗性,这突出表明在仅基于啮齿动物数据确定逆行载体是否适合 NHP 研究时需要谨慎。