Single-cell transcriptomic analysis of the adult mouse spinal cord reveals molecular diversity of autonomic and skeletal motor neurons

被引:117
作者
Blum, Jacob A. [1 ]
Klemm, Sandy [1 ]
Shadrach, Jennifer L. [3 ]
Guttenplan, Kevin A. [1 ,2 ]
Nakayama, Lisa [1 ]
Kathiria, Arwa [1 ]
Hoang, Phuong T. [1 ,4 ]
Gautier, Olivia [1 ,2 ]
Kaltschmidt, Julia A. [3 ]
Greenleaf, William J. [1 ,5 ,6 ]
Gitler, Aaron D. [1 ]
机构
[1] Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Stanford Neurosci Grad Program, Sch Med, Stanford, CA USA
[3] Stanford Univ, Dept Neurosurg, Sch Med, Stanford, CA USA
[4] Stanford Univ, Dept Neurol & Neurol Sci, Sch Med, Stanford, CA USA
[5] Stanford Univ, Dept Appl Phys, Stanford, CA 94305 USA
[6] Chan Zuckerberg Biohub, San Francisco, CA USA
基金
美国国家卫生研究院;
关键词
SYMPATHETIC PREGANGLIONIC NEURONS; CONNECTIVITY; INTERNEURONS; SPECIFICITY; GAMMA; INNERVATION; GENERATION; PATHWAYS; SUBTYPES; MARKER;
D O I
10.1038/s41593-020-00795-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The spinal cord is a fascinating structure that is responsible for coordinating movement in vertebrates. Spinal motor neurons control muscle activity by transmitting signals from the spinal cord to diverse peripheral targets. In this study, we profiled 43,890 single-nucleus transcriptomes from the adult mouse spinal cord using fluorescence-activated nuclei sorting to enrich for motor neuron nuclei. We identified 16 sympathetic motor neuron clusters, which are distinguishable by spatial localization and expression of neuromodulatory signaling genes. We found surprising skeletal motor neuron heterogeneity in the adult spinal cord, including transcriptional differences that correlate with electrophysiologically and spatially distinct motor pools. We also provide evidence for a novel transcriptional subpopulation of skeletal motor neuron (gamma*). Collectively, these data provide a single-cell transcriptional atlas (http://spinalcordatlas.org) for investigating the organizing molecular logic of adult motor neuron diversity, as well as the cellular and molecular basis of motor neuron function in health and disease.
引用
收藏
页码:572 / 583
页数:12
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