Massively Parallel Single Nucleus Transcriptional Profiling Defines Spinal Cord Neurons and Their Activity during Behavior

被引:247
作者
Sathyamurthy, Anupama [1 ]
Johnson, Kory R. [2 ]
Matson, Kaya J. E. [1 ]
Dobrott, Courtney I. [1 ]
Li, Li [1 ]
Ryba, Anna R. [1 ]
Bergman, Tzipporah B. [1 ]
Kelly, Michael C. [3 ]
Kelley, Matthew W. [3 ]
Levine, Ariel J. [1 ]
机构
[1] Natl Inst Neurol Disorders & Stroke, Spinal Circuits & Plast Unit, Bethesda, MD 20892 USA
[2] Natl Inst Neurol Disorders & Stroke, Informat Technol Program, Bioinformat Sect, Bethesda, MD 20892 USA
[3] Natl Inst Deafness & Other Commun Disorders, Lab Cochlear Dev, Bethesda, MD 20892 USA
关键词
CELL RNA-SEQ; NITRIC-OXIDE SYNTHASE; DORSAL-HORN; INHIBITORY INTERNEURONS; NOXIOUS-STIMULATION; MECHANICAL PAIN; MOTOR CONTROL; DIVERSITY; RAT; FOS;
D O I
10.1016/j.celrep.2018.02.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To understand the cellular basis of behavior, it is necessary to know the cell types that exist in the nervous system and their contributions to function. Spinal networks are essential for sensory processing and motor behavior and provide a powerful system for identifying the cellular correlates of behavior. Here, we used massively parallel single nucleus RNA sequencing (snRNA-seq) to create an atlas of the adult mouse lumbar spinal cord. We identified and molecularly characterized 43 neuronal populations. Next, we leveraged the snRNA-seq approach to provide unbiased identification of neuronal populations that were active following a sensory and a motor behavior, using a transcriptional signature of neuronal activity. This approach can be used in the future to link single nucleus gene expression data with dynamic biological responses to behavior, injury, and disease.
引用
收藏
页码:2216 / 2225
页数:10
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