共 50 条
Viral vectors for neuronal cell type-specific visualization and manipulations
被引:15
|作者:
Liu, Yuanyuan
[1
]
Hegarty, Shane
[2
,3
,4
]
Winter, Carla
[2
,3
,5
]
Wang, Fan
[6
]
He, Zhigang
[2
,3
,4
]
机构:
[1] Natl Inst Dent & Craniofacial Res NIDCR, Somatosensat & Pain Unit, Natl Ctr Complementary & Integrat Hlth NCCIH, Natl Inst Hlth NIH, Bethesda, MD USA
[2] Boston Childrens Hosp, FM Kirby Neurobiol Ctr, Boston, MA 02115 USA
[3] Boston Childrens Hosp, Dept Neurol, Boston, MA 02115 USA
[4] Harvard Med Sch, Dept Neurol, Boston, MA 02115 USA
[5] Harvard Med Sch, PhD Program Biol & Biomed Sci, Boston, MA 02115 USA
[6] Duke Univ, Med Ctr, Dept Neurobiol, Durham, NC 27710 USA
关键词:
ADENOASSOCIATED VIRUS AAV;
GENETIC DISSECTION;
NEURAL CIRCUITS;
NERVOUS-SYSTEM;
RABIES;
DELIVERY;
TROPISM;
ORGANIZATION;
INTERNEURONS;
SEROTYPE-8;
D O I:
10.1016/j.conb.2020.03.011
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Characterizing neuronal cell types demands efficient strategies for specific labeling and manipulation of individual subtypes to dissect their connectivity and functions. Recombinant viral technology offers a powerful toolbox for targeted transgene expression in specific neuronal populations. In order to achieve cell type-specific targeting, exciting progress has been made to: alter viral tropisms, design rational delivery strategies, and drive selective expression patterns with engineered DNA sequences in viral genomes. For the latter case, emerging single-cell genomic analyses provide rich databases. In this review, we will summarize current status, and point out challenges, of using viral vectors for neuronal cell type-specific visualization and manipulations. With concerted efforts, progress will continue to be made toward developing viral vectors for the vast array of neuronal subtypes in the mammalian nervous system.
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页码:67 / 76
页数:10
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