Dissecting local circuits in vivo: Integrated optogenetic and electrophysiology approaches for exploring inhibitory regulation of cortical activity

被引:38
作者
Cardin, Jessica A. [1 ]
机构
[1] Yale Univ, Dept Neurobiol, New Haven, CT 06520 USA
关键词
Interneuron; Inhibition; Fast-spiking; Somatostatin; Optogenetics; Channelrhodopsin; Halorhodopsin; Archaerhodopsin; Electrophysiology; Tetrode; ADENOASSOCIATED VIRUS; MOUSE-BRAIN; MILLISECOND-TIMESCALE; 2-PHOTON EXCITATION; NEURONAL MIGRATION; OPTICAL CONTROL; GENE-TRANSFER; INTERNEURONS; EXPRESSION; CHANNELRHODOPSIN-2;
D O I
10.1016/j.jphysparis.2011.09.005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Local cortical circuit activity in vivo comprises a complex and flexible series of interactions between excitatory and inhibitory neurons. Our understanding of the functional interactions between these different neural populations has been limited by the difficulty of identifying and selectively manipulating the diverse and sparsely represented inhibitory interneuron classes in the intact brain. The integration of recently developed optical tools with traditional electrophysiological techniques provides a powerful window into the role of inhibition in regulating the activity of excitatory neurons. In particular, optogenetic targeting of specific cell classes reveals the distinct impacts of local inhibitory populations on other neurons in the surrounding local network. In addition to providing the ability to activate or suppress spiking in target cells, optogenetic activation identifies extracellularly recorded neurons by class, even when naturally occurring spike rates are extremely low. However, there are several important limitations on the use of these tools and the interpretation of resulting data. The purpose of this article is to outline the uses and limitations of optogenetic tools, along with current methods for achieving cell type-specific expression, and to highlight the advantages of an experimental approach combining optogenetics and electrophysiology to explore the role of inhibition in active networks. To illustrate the efficacy of these combined approaches, I present data comparing targeted manipulations of cortical fast-spiking, parvalbumin-expressing and low threshold-spiking, somatostatin-expressing interneurons in vivo. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:104 / 111
页数:8
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