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Conserved cell types with divergent features in human versus mouse cortex
- Source :
- Nature, vol 573, iss 7772, Nature, 573(7772), 61
- Publication Year :
- 2019
-
Abstract
- Elucidating the cellular architecture of the human cerebral cortex is central to understanding our cognitive abilities and susceptibility to disease. Here we used single-nucleus RNA-sequencing analysis to perform a comprehensive study of cell types in the middle temporal gyrus of human cortex. We identified a highly diverse set of excitatory and inhibitory neuron types that are mostly sparse, with excitatory types being less layer-restricted than expected. Comparison to similar mouse cortex single-cell RNA-sequencing datasets revealed a surprisingly well-conserved cellular architecture that enables matching of homologous types and predictions of properties of human cell types. Despite this general conservation, we also found extensive differences between homologous human and mouse cell types, including marked alterations in proportions, laminar distributions, gene expression and morphology. These species-specific features emphasize the importance of directly studying human brain.
- Subjects :
- 0301 basic medicine
Adult
Male
Cell type
Adolescent
General Science & Technology
Middle temporal gyrus
1.1 Normal biological development and functioning
Biology
03 medical and health sciences
Mice
Young Adult
0302 clinical medicine
Single-cell analysis
Species Specificity
Underpinning research
Cortex (anatomy)
medicine
Genetics
Animals
Humans
2.1 Biological and endogenous factors
RNA-Seq
Aetiology
Aged
Cerebral Cortex
Neurons
Principal Component Analysis
Multidisciplinary
Cellular architecture
Neurosciences
Neural Inhibition
Human brain
Middle Aged
Biological Evolution
030104 developmental biology
medicine.anatomical_structure
Cerebral cortex
Astrocytes
Neurological
Excitatory postsynaptic potential
Female
Single-Cell Analysis
Transcriptome
Neuroscience
030217 neurology & neurosurgery
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Nature, vol 573, iss 7772, Nature, 573(7772), 61
- Accession number :
- edsair.doi.dedup.....45cb2e1e03c5b89538fe61c3d31c48fc
- Full Text :
- https://doi.org/10.1038/s41586-019-1506-7