Abstract

To understand the cellular composition and region-specific specialization of white matter — a disease-relevant, glia-rich tissue highly expanded in primates relative to rodents — we profiled transcriptomes of ~500,000 nuclei from 19 tissue types of the central nervous system of healthy common marmoset and mapped 87 subclusters spatially onto a 3D MRI atlas. We performed cross-species comparison, explored regulatory pathways, modeled regional intercellular communication, and surveyed cellular determinants of neurological disorders. Here, we analyze this resource and find strong spatial segregation of microglia, oligodendrocyte progenitor cells, and astrocytes. White matter glia are diverse, enriched with genes involved in stimulus-response and biomolecule modification, and predicted to interact with other resident cells more extensively than their gray matter counterparts. Conversely, gray matter glia preserve the expression of neural tube patterning genes into adulthood and share six transcription factors that restrict transcriptome complexity. A companion Callithrix jacchus Primate Cell Atlas (CjPCA) is available through https://cjpca.ninds.nih.gov.

Studies of cell heterogeneity in white matter in primates have been limited to date. Here the authors describe a marmoset brain cell atlas that bridges rodent and human data, revealing strong gray-white matter glial segregation.

Details

Title
Transcriptomic architecture of nuclei in the marmoset CNS
Author
Lin, Jing-Ping 1   VIAFID ORCID Logo  ; Kelly, Hannah M. 1 ; Song, Yeajin 1 ; Kawaguchi, Riki 2 ; Geschwind, Daniel H. 3   VIAFID ORCID Logo  ; Jacobson, Steven 4 ; Reich, Daniel S. 1   VIAFID ORCID Logo 

 National Institutes of Health, Translational Neuroradiology Section, National Institute of Neurological Disorders and Stroke, Bethesda, USA (GRID:grid.94365.3d) (ISNI:0000 0001 2297 5165) 
 University of California, Los Angeles, Psychiatry, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, Los Angeles, USA (GRID:grid.19006.3e) (ISNI:0000 0000 9632 6718) 
 University of California, Los Angeles, Psychiatry, Semel Institute for Neuroscience and Human Behavior, David Geffen School of Medicine, Los Angeles, USA (GRID:grid.19006.3e) (ISNI:0000 0000 9632 6718); University of California, Los Angeles, Departments of Neurology and Human Genetics, Los Angeles, USA (GRID:grid.19006.3e) (ISNI:0000 0000 9632 6718) 
 National Institutes of Health, Viral Immunology Section, National Institute of Neurological Disorders and Stroke, Bethesda, USA (GRID:grid.94365.3d) (ISNI:0000 0001 2297 5165) 
Publication year
2022
Publication date
2022
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2716391153
Copyright
© This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.