| Literature DB >> 30096299 |
Arpiar Saunders1, Evan Z Macosko2, Alec Wysoker3, Melissa Goldman3, Fenna M Krienen3, Heather de Rivera3, Elizabeth Bien3, Matthew Baum3, Laura Bortolin3, Shuyu Wang4, Aleksandrina Goeva4, James Nemesh3, Nolan Kamitaki3, Sara Brumbaugh3, David Kulp3, Steven A McCarroll5.
Abstract
The mammalian brain is composed of diverse, specialized cell populations. To systematically ascertain and learn from these cellular specializations, we used Drop-seq to profile RNA expression in 690,000 individual cells sampled from 9 regions of the adult mouse brain. We identified 565 transcriptionally distinct groups of cells using computational approaches developed to distinguish biological from technical signals. Cross-region analysis of these 565 cell populations revealed features of brain organization, including a gene-expression module for synthesizing axonal and presynaptic components, patterns in the co-deployment of voltage-gated ion channels, functional distinctions among the cells of the vasculature and specialization of glutamatergic neurons across cortical regions. Systematic neuronal classifications for two complex basal ganglia nuclei and the striatum revealed a rare population of spiny projection neurons. This adult mouse brain cell atlas, accessible through interactive online software (DropViz), serves as a reference for development, disease, and evolution.Entities:
Keywords: basal ganglia; brain; single-cell; striatum; transcriptional programs
Mesh:
Year: 2018 PMID: 30096299 PMCID: PMC6447408 DOI: 10.1016/j.cell.2018.07.028
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582