In Vivo Interrogation of Spinal Mechanosensory Circuits

被引:56
作者
Christensen, Amelia J. [1 ]
Iyer, Shrivats M. [2 ]
Francois, Amaury [3 ,4 ]
Vyas, Saurabh [2 ]
Ramakrishnan, Charu [2 ]
Vesuna, Sam [2 ]
Deisseroth, Karl [2 ,5 ,6 ]
Scherrer, Gregory [3 ,4 ,7 ,8 ]
Delp, Scott L. [2 ,9 ]
机构
[1] Stanford Univ, Dept Elect Engn, 318 Campus Dr, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Bioengn, 318 Campus Dr, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Anesthesiol Perioperat & Pain Med, 318 Campus Dr, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Mol & Cellular Physiol, 318 Campus Dr, Stanford, CA 94305 USA
[5] Stanford Univ, Dept Psychiat & Behav Sci, 318 Campus Dr, Stanford, CA 94305 USA
[6] Stanford Univ, Howard Hughes Med Inst, 318 Campus Dr, Stanford, CA 94305 USA
[7] Stanford Univ, Dept Neurosurg, 318 Campus Dr, Stanford, CA 94305 USA
[8] Stanford Univ, Dept Stanford Neurosci Inst, 318 Campus Dr, Stanford, CA 94305 USA
[9] Stanford Univ, Dept Mech Engn, 318 Campus Dr, Stanford, CA 94305 USA
来源
CELL REPORTS | 2016年 / 17卷 / 06期
关键词
OPTOGENETICS; 10; YEARS; DORSAL-HORN; PARVALBUMIN NEURONS; GAIT ANALYSIS; PAIN; CORD; RECEPTORS; MICE; RAT; LOCOMOTION;
D O I
10.1016/j.celrep.2016.10.010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Spinal dorsal horn circuits receive, process, and transmit somatosensory information. To understand how specific components of these circuits contribute to behavior, it is critical to be able to directlymodulate their activity in unanesthetized in vivo conditions. Here, we develop experimental tools that enable optogenetic control of spinal circuitry in freely moving mice using commonly available materials. We use thesetools to examineme chanosensory processing in the spinal cord and observe that optogenetic activation of somatostatin-positive interneurons facilitates both mechanosensory and itch-related behavior, while reversible chemogenetic inhibition of these neurons suppresses mechanosensation. These results extend recent findings regarding the processing of mechanosensory information in the spinal cord and indicate the potential for activity-induced release of the somatostatin neuropeptide to affect processing of itch. The spinal implant approach we describe here is likely to enable a wide range of studies to elucidate spinal circuits underlying pain, touch, itch, and movement.
引用
收藏
页码:1699 / 1710
页数:12
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