Interindividual variation in human cortical cell type abundance and expression

Author:

Johansen Nelson1ORCID,Somasundaram Saroja1ORCID,Travaglini Kyle J.1ORCID,Yanny Anna Marie1,Shumyatcher Maya1,Casper Tamara1ORCID,Cobbs Charles2ORCID,Dee Nick1ORCID,Ellenbogen Richard3ORCID,Ferreira Manuel3,Goldy Jeff1ORCID,Guzman Junitta1ORCID,Gwinn Ryder2ORCID,Hirschstein Daniel1,Jorstad Nikolas L.1ORCID,Keene C. Dirk4ORCID,Ko Andrew3ORCID,Levi Boaz P.1ORCID,Ojemann Jeffrey G.3ORCID,Pham Thanh1ORCID,Shapovalova Nadiya1ORCID,Silbergeld Daniel3,Sulc Josef1ORCID,Torkelson Amy1ORCID,Tung Herman1ORCID,Smith Kimberly1ORCID,Lein Ed S.1ORCID,Bakken Trygve E.1ORCID,Hodge Rebecca D.1ORCID,Miller Jeremy A.1ORCID

Affiliation:

1. Allen Institute for Brain Science, Seattle, WA 98109, USA.

2. Swedish Neuroscience Institute, Seattle,WA 98122, USA.

3. Department of Neurological Surgery, University of Washington, Seattle, WA 98104, USA.

4. Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA 98104, USA.

Abstract

Single-cell transcriptomic studies have identified a conserved set of neocortical cell types from small postmortem cohorts. We extended these efforts by assessing cell type variation across 75 adult individuals undergoing epilepsy and tumor surgeries. Nearly all nuclei map to one of 125 robust cell types identified in the middle temporal gyrus. However, we found interindividual variance in abundances and gene expression signatures, particularly in deep-layer glutamatergic neurons and microglia. A minority of donor variance is explainable by age, sex, ancestry, disease state, and cell state. Genomic variation was associated with expression of 150 to 250 genes for most cell types. This characterization of cellular variation provides a baseline for cell typing in health and disease.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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