Targeting Single Neuronal Networks for Gene Expression and Cell Labeling In Vivo

被引:146
作者
Marshel, James H. [1 ,2 ]
Mori, Takuma [1 ]
Nielsen, Kristina J. [1 ]
Callaway, Edward M. [1 ,2 ]
机构
[1] Salk Inst Biol Studies, Syst Neurobiol Labs, La Jolla, CA 92037 USA
[2] Univ Calif San Diego, Grad Program Neurosci, La Jolla, CA 92037 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
CENTRAL-NERVOUS-SYSTEM; RABIES VIRUS; CEREBRAL-CORTEX; TRANSNEURONAL TRACER; SYNAPTIC CONNECTIONS; PYRAMIDAL NEURONS; VISUAL-CORTEX; BARREL CORTEX; PREFRONTAL CORTEX; AVIAN-LEUKOSIS;
D O I
10.1016/j.neuron.2010.08.001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
To understand fine-scale structure and function of single mammalian neuronal networks, we developed and validated a strategy to genetically target and trace monosynaptic inputs to a single neuron in vitro and in vivo. The strategy independently targets a neuron and its presynaptic network for specific gene expression and fine-scale labeling, using single-cell electroporation of DNA to target infection and monosynaptic retrograde spread of a genetically modifiable rabies virus. The technique is highly reliable, with transsynaptic labeling occurring in every electroporated neuron infected by the virus. Targeting single neocortical neuronal networks in vivo, we found clusters of both spiny and aspiny neurons surrounding the electroporated neuron in each case, in addition to intricately labeled distal cortical and subcortical inputs. This technique, broadly applicable for probing and manipulating single neuronal networks with single-cell resolution in vivo, may help shed new light on fundamental mechanisms underlying circuit development and information processing by neuronal networks throughout the brain.
引用
收藏
页码:562 / 574
页数:13
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