衣壳
神经科学
生物
转导(生物物理学)
基因传递
转基因
腺相关病毒
向性
组织向性
电池类型
效应器
报告基因
基因
计算生物学
细胞生物学
基因表达
细胞
遗传增强
病毒
重组DNA
病毒学
遗传学
载体(分子生物学)
生物化学
作者
Rosemary C. Challis,Sripriya Ravindra Kumar,Xinhong Chen,David Goertsen,Gerard Michael Coughlin,Acacia M Hori,Miguel R. Chuapoco,Thomas S. Otis,Timothy F. Miles,Viviana Gradinaru
出处
期刊:Annual Review of Neuroscience
[Annual Reviews]
日期:2022-04-20
卷期号:45 (1): 447-469
被引量:78
标识
DOI:10.1146/annurev-neuro-111020-100834
摘要
Recombinant adeno-associated viruses (AAVs) are commonly used gene delivery vehicles for neuroscience research. They have two engineerable features: the capsid (outer protein shell) and cargo (encapsulated genome). These features can be modified to enhance cell type or tissue tropism and control transgene expression, respectively. Several engineered AAV capsids with unique tropisms have been identified, including variants with enhanced central nervous system transduction, cell type specificity, and retrograde transport in neurons. Pairing these AAVs with modern gene regulatory elements and state-of-the-art reporter, sensor, and effector cargo enables highly specific transgene expression for anatomical and functional analyses of brain cells and circuits. Here, we discuss recent advances that provide a comprehensive (capsid and cargo) AAV toolkit for genetic access to molecularly defined brain cell types.
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