Chen Yefei, Wang Jingyi, Liu Jing, Lin Jianbang, Lin Yunping, Nie Jinyao, Yue Qi, Deng Chunshan, Qi Xiaofei, Li Yuantao, Dai Ji, Lu Zhonghua
Department of Anesthesiology, Shenzhen Maternity and Child Healthcare Hospital, The First School of Clinical Medicine, Southern Medical University, Shenzhen, 518027, China.
Shenzhen Technological Research Center for Primate Translational Medicine, Shenzhen Key Laboratory for Molecular Biology of Neural Development, Shenzhen-Hong Kong Institute of Brain Science, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, China.
Neurosci Bull. 2024 Jan;40(1):90-102. doi: 10.1007/s12264-023-01091-0. Epub 2023 Jul 11.
Retrograde adeno-associated viruses (AAVs) are capable of infecting the axons of projection neurons and serve as a powerful tool for the anatomical and functional characterization of neural networks. However, few retrograde AAV capsids have been shown to offer access to cortical projection neurons across different species and enable the manipulation of neural function in non-human primates (NHPs). Here, we report the development of a novel retrograde AAV capsid, AAV-DJ8R, which efficiently labeled cortical projection neurons after local administration into the striatum of mice and macaques. In addition, intrastriatally injected AAV-DJ8R mediated opsin expression in the mouse motor cortex and induced robust behavioral alterations. Moreover, AAV-DJ8R markedly increased motor cortical neuron firing upon optogenetic light stimulation after viral delivery into the macaque putamen. These data demonstrate the usefulness of AAV-DJ8R as an efficient retrograde tracer for cortical projection neurons in rodents and NHPs and indicate its suitability for use in conducting functional interrogations.
逆行腺相关病毒(AAV)能够感染投射神经元的轴突,是用于神经网络解剖学和功能特征研究的强大工具。然而,很少有逆行AAV衣壳能够跨不同物种进入皮质投射神经元,并实现对非人灵长类动物(NHP)神经功能的操纵。在此,我们报告了一种新型逆行AAV衣壳AAV-DJ8R的开发,将其局部注射到小鼠和猕猴的纹状体后,能有效标记皮质投射神经元。此外,纹状体内注射的AAV-DJ8R介导了小鼠运动皮质中的视蛋白表达,并诱导了强烈的行为改变。而且,将病毒注射到猕猴壳核后,AAV-DJ8R在光遗传学光刺激下显著增加了运动皮质神经元的放电。这些数据证明了AAV-DJ8R作为啮齿动物和NHP中皮质投射神经元的有效逆行示踪剂的实用性,并表明其适用于进行功能研究。
Neurosci Lett. 2022-7-27
J Neurosci Methods. 2020-11-1
Innovation (Camb). 2022-12-5
Neurosci Bull. 2022-12
Neurosci Bull. 2022-11
J Neurosci Methods. 2020-11-1