Disease-associated astrocytes and microglia markers are upregulated in mice fed high fat diet

Author:

Lin Li,Basu Rashmita,Chatterjee Debolina,Templin Andrew T.,Flak Jonathan N.,Johnson Travis S.

Abstract

AbstractHigh-fat diet (HFD) is associated with Alzheimer’s disease (AD) and type 2 diabetes risk, which share features such as insulin resistance and amylin deposition. We examined gene expression associated with astrocytes and microglia since dysfunction of these cell types is implicated in AD pathogenesis. We hypothesize gene expression changes in disease-associated astrocytes (DAA), disease-associated microglia and human Alzheimer’s microglia exist in diabetic and obese individuals before AD development. By analyzing bulk RNA-sequencing (RNA-seq) data generated from brains of mice fed HFD and humans with AD, 11 overlapping AD-associated differentially expressed genes were identified, including Kcnj2, C4b and Ddr1, which are upregulated in response to both HFD and AD. Analysis of single cell RNA-seq (scRNA-seq) data indicated C4b is astrocyte specific. Spatial transcriptomics (ST) revealed C4b colocalizes with Gfad, a known astrocyte marker, and the colocalization of C4b expressing cells with Gad2 expressing cells, i.e., GABAergic neurons, in mouse brain. There also exists a positive correlation between C4b and Gad2 expression in ST indicating a potential interaction between DAA and GABAergic neurons. These findings provide novel links between the pathogenesis of obesity, diabetes and AD and identify C4b as a potential early marker for AD in obese or diabetic individuals.

Funder

the Indiana University Center for Diabetes and Metabolic Disease Pilot and Feasibility Program

the US Department of Veterans Affairs

Indiana Biosciences Research Institute

the American Diabetes Association Pathway Program

National Institute of Health National Institute of General Medical Sciences

the Indiana University Precision Health Initiative Funding

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

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