An Adeno-Associated Virus-Based Toolkit for Preferential Targeting and Manipulating Quiescent Neural Stem Cells in the Adult Hippocampus

被引:9
作者
Crowther, Andrew J. [1 ,2 ,3 ]
Lim, Szu-Aun [1 ,2 ]
Asrican, Brent [1 ,2 ]
Albright, Blake H. [4 ,5 ,6 ]
Wooten, Josh [1 ,2 ,6 ]
Yeh, Chia-Yu [1 ,2 ]
Bao, Hechen [1 ,2 ]
Cerri, Domenic H. [7 ,8 ]
Hu, Jessica [1 ,2 ]
Shih, Yen-Yu Ian [7 ,8 ]
Asokan, Aravind [4 ,5 ,6 ]
Song, Juan [1 ,2 ,3 ,6 ]
机构
[1] Univ N Carolina, Dept Pharmacol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Neurosci Ctr, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Neurobiol Curriculum, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Dept Genet, Chapel Hill, NC 27599 USA
[5] Univ N Carolina, Gene Therapy Ctr, Chapel Hill, NC 27599 USA
[6] Univ N Carolina, Genet & Mol Biol Curriculum, Chapel Hill, NC 27599 USA
[7] Univ N Carolina, Dept Neurol, Chapel Hill, NC 27599 USA
[8] Univ N Carolina, Biomed Res Imaging Ctr, Chapel Hill, NC 27599 USA
关键词
IN-VIVO; ANALYSIS REVEALS; MAMMALIAN BRAIN; NERVOUS-SYSTEM; VIRAL VECTORS; SIALIC ACIDS; NEUROGENESIS; FATE; INTERNEURONS; TRANSDUCTION;
D O I
10.1016/j.stemcr.2018.01.018
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Quiescent neural stem cells (qNSCs) with radial morphology are the only proven source of new neurons in the adult mammalian brain. Our understanding of the roles of newly generated neurons depends on the ability to target and manipulate adult qNSCs. Although various strategies have been developed to target and manipulate adult hippocampal qNSCs, they often suffer from prolonged breeding, low recombination efficiency, and non-specific labeling. Therefore, developing a readily manufactured viral vector that allows flexible packaging and robust expression of various transgenes in qNSCs is a pressing need. Here, we report a recombinant adeno-associated virus serotype 4 (rAAV4)-based toolkit that preferentially targets hippocampal qNSCs and allows for lineage tracing, functional analyses, and activity manipulation of adult qNSCs. Importantly, targeting qNSCs in a non-Cre-dependent fashion opens the possibility for studying qNSCs in less genetically tractable animal species and may have translational impact in gene therapy by preferentially targeting qNSCs.
引用
收藏
页码:1146 / 1159
页数:14
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