Direct Visualization of the Murine Dorsal Cochlear Nucleus for Optogenetic Stimulation of the Auditory Pathway

被引:10
作者
Kozin, Elliott D. [1 ]
Darrow, Keith N. [2 ]
Hight, Ariel E. [1 ]
Lehmann, Ashton E. [1 ]
Kaplan, Alyson B. [1 ]
Brown, M. Christian [1 ]
Lee, Daniel J. [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Otol & Laryngol, Cambridge, MA 02138 USA
[2] Worcester State Univ, Dept Commun Sci & Disorders, Worcester, MA 01602 USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2015年 / 95期
基金
美国国家卫生研究院;
关键词
Neuroscience; Issue; 95; Optogenetics; dorsal cochlear nucleus; virus-mediated gene transfer; auditory system; GENE-THERAPY; MOTOR CORTEX; GUINEA-PIG; MOUSE; NEURONS; RATS; CHANNELRHODOPSIN-2; CONSOLIDATION; MODULATION; EXPRESSION;
D O I
10.3791/52426
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Investigation into the use of virus-mediated gene transfer to arrest or reverse hearing loss has largely been relegated to the peripheral auditory system. Few studies have examined gene transfer to the central auditory system. The dorsal cochlear nucleus (DCN) of the brainstem, which contains second order neurons of the auditory pathway, is a potential site for gene transfer. In this protocol, a technique for direct and maximal exposure of the murine DCN via a posterior fossa approach is demonstrated. This approach allows for either acute or survival surgery. Following direct visualization of the DCN, a host of experiments are possible, including injection of opsins into the cochlear nucleus and subsequent stimulation by an optical fiber coupled to a blue light laser. Other neurophysiology experiments, such as electrical stimulation and neural injector tracings are also feasible. The level of visualization and the duration of stimulation achievable make this approach applicable to a wide range of experiments.
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页数:6
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