An AAV capsid proposed as microglia-targeting directs genetic expression in forebrain excitatory neurons.

IF 4.3 Q1 BIOCHEMICAL RESEARCH METHODS
Wenhao Cao, Zhiqun Tan, Bereket T Berackey, Jason K Nguyen, Sara R Brown, Shiyang Du, Bin Lin, Qiao Ye, Magdalene Seiler, Todd C Holmes, Xiangmin Xu
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引用次数: 0

Abstract

A newly developed capsid AAV-MG1.2 was reported to mediate specific microglial transduction. However, we find that AAV-MG1.2 actually enables specific genetic access to excitatory neurons in forebrain regions including hippocampal formation and visual cortex but does not confer expression in microglia or astrocytes in vivo. Furthermore, we find that AAV-MG1.2 specifically labels the deep layer of the CA1 pyramidal layer in a titer-dependent manner. We show that AAV-MG1.2-Cre can be used to genetically target excitatory neurons for cell-type-specific neural circuit mapping studies. We also find that AAV-MG1.2 conserves specificity for excitatory neurons in rat hippocampus. Thus, the AAV-MG1.2 presents a useful viral-genetic tool for targeting excitatory neurons in the forebrain across different species.

一种AAV衣壳被提出作为小胶质细胞靶向指导前脑兴奋性神经元的基因表达。
据报道,新开发的衣壳AAV-MG1.2介导特异性小胶质细胞转导。然而,我们发现AAV-MG1.2实际上可以通过特定的遗传途径进入包括海马和视觉皮层在内的前脑区域的兴奋性神经元,但在体内却不能在小胶质细胞或星形胶质细胞中表达。此外,我们发现AAV-MG1.2以滴度依赖的方式特异性标记CA1锥体层的深层。我们发现AAV-MG1.2-Cre可以用于基因靶向兴奋性神经元,用于细胞类型特异性神经回路定位研究。我们还发现AAV-MG1.2保留了对大鼠海马兴奋性神经元的特异性。因此,AAV-MG1.2是一种针对不同物种前脑兴奋性神经元的有用病毒遗传工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell Reports Methods
Cell Reports Methods Chemistry (General), Biochemistry, Genetics and Molecular Biology (General), Immunology and Microbiology (General)
CiteScore
3.80
自引率
0.00%
发文量
0
审稿时长
111 days
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