A transcriptomic taxonomy of mouse brain-wide spinal projecting neurons

被引:15
|
作者
Winter, Carla C. [1 ,2 ,3 ,4 ,5 ]
Jacobi, Anne [1 ,2 ,3 ,12 ]
Su, Junfeng [1 ,2 ,3 ]
Chung, Leeyup [1 ,2 ,3 ]
van Velthoven, Cindy T. J. [6 ]
Yao, Zizhen [6 ]
Lee, Changkyu [6 ]
Zhang, Zicong [1 ,2 ,3 ]
Yu, Shuguang [1 ,2 ,3 ]
Gao, Kun [7 ,8 ]
Duque Salazar, Geraldine [1 ,2 ,3 ]
Kegeles, Evgenii [1 ,2 ,3 ,4 ]
Zhang, Yu [1 ,2 ,3 ]
Tomihiro, Makenzie C. [1 ,2 ,3 ]
Zhang, Yiming [1 ,2 ,3 ]
Yang, Zhiyun [1 ,2 ,3 ]
Zhu, Junjie [1 ,2 ,3 ]
Tang, Jing [1 ,2 ,3 ]
Song, Xuan [1 ,2 ,3 ]
Donahue, Ryan J. [1 ,2 ,3 ]
Wang, Qing [7 ,8 ]
Mcmillen, Delissa [6 ]
Kunst, Michael [6 ]
Wang, Ning [6 ]
Smith, Kimberly A. [6 ]
Romero, Gabriel E. [9 ]
Frank, Michelle M. [9 ]
Krol, Alexandra [10 ]
Kawaguchi, Riki [7 ,8 ]
Geschwind, Daniel H. [7 ,8 ]
Feng, Guoping [10 ]
Goodrich, Lisa V. [9 ]
Liu, Yuanyuan [11 ]
Tasic, Bosiljka [6 ]
Zeng, Hongkui [6 ]
He, Zhigang [1 ,2 ,3 ]
机构
[1] Boston Childrens Hosp, FM Kirby Neurobiol Ctr, Boston, MA 02115 USA
[2] Harvard Med Sch, Dept Neurol, Boston, MA 02115 USA
[3] Harvard Med Sch, Dept Ophthalmol, Boston, MA 02115 USA
[4] Harvard Med Sch, PhD Program Biol & Biomed Sci, Boston, MA USA
[5] Harvard Med Sch, Harvard MIT MD PhD Program, Boston, MA 02115 USA
[6] Allen Inst Brain Sci, Seattle, WA 98109 USA
[7] Univ Calif Los Angeles, Semel Inst Neurosci & Human Behav, David Geffen Sch Med, Los Angeles, CA USA
[8] Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Program Neurogenet, Los Angeles, CA USA
[9] Harvard Med Sch, Dept Neurobiol, Boston, MA USA
[10] MIT, McGovern Inst Brain Res, Dept Brain & Cognit Sci, Cambridge, MA USA
[11] Natl Inst Dent & Craniofacial Res, Somatosensat & Pain Unit, Natl Ctr Complementary & Integrat Hlth, NIH, Bethesda, MD USA
[12] F Hoffman La Roche AG, pRED, Basel, Switzerland
基金
美国国家卫生研究院;
关键词
CELL-TYPE; PATHWAYS; CIRCUITS; CORD; NUCLEUS; GENES; STEM;
D O I
10.1038/s41586-023-06817-8
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
The brain controls nearly all bodily functions via spinal projecting neurons (SPNs) that carry command signals from the brain to the spinal cord. However, a comprehensive molecular characterization of brain-wide SPNs is still lacking. Here we transcriptionally profiled a total of 65,002 SPNs, identified 76 region-specific SPN types, and mapped these types into a companion atlas of the whole mouse brain1. This taxonomy reveals a three-component organization of SPNs: (1) molecularly homogeneous excitatory SPNs from the cortex, red nucleus and cerebellum with somatotopic spinal terminations suitable for point-to-point communication; (2) heterogeneous populations in the reticular formation with broad spinal termination patterns, suitable for relaying commands related to the activities of the entire spinal cord; and (3) modulatory neurons expressing slow-acting neurotransmitters and/or neuropeptides in the hypothalamus, midbrain and reticular formation for 'gain setting' of brain-spinal signals. In addition, this atlas revealed a LIM homeobox transcription factor code that parcellates the reticulospinal neurons into five molecularly distinct and spatially segregated populations. Finally, we found transcriptional signatures of a subset of SPNs with large soma size and correlated these with fast-firing electrophysiological properties. Together, this study establishes a comprehensive taxonomy of brain-wide SPNs and provides insight into the functional organization of SPNs in mediating brain control of bodily functions. In this study, the authors develop a comprehensive taxonomy of brain-wide SPNs, identifying several novel subsets via their transcriptional signatures.
引用
收藏
页码:403 / 414
页数:53
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