4.8 Article

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

期刊

CELL REPORTS
卷 22, 期 8, 页码 2216-2225

出版社

CELL PRESS
DOI: 10.1016/j.celrep.2018.02.003

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资金

  1. NIH Intramural Research Program from the NINDS [1 ZIA NS003153 02]
  2. NIH Intramural Research Program from the NIDCD [1 ZIA DC000059 18]
  3. NIH grant [2 U42 OD011158]
  4. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [ZIANS003153] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS [ZIADC000059] Funding Source: NIH RePORTER
  6. OFFICE OF THE DIRECTOR, NATIONAL INSTITUTES OF HEALTH [U42OD011158] Funding Source: NIH RePORTER

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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.

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