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

High-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...

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Autores principales: Lin, Li, Basu, Rashmita, Chatterjee, Debolina, Templin, Andrew T., Flak, Jonathan N., Johnson, Travis S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10412627/
https://www.ncbi.nlm.nih.gov/pubmed/37558676
http://dx.doi.org/10.1038/s41598-023-39890-0
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author Lin, Li
Basu, Rashmita
Chatterjee, Debolina
Templin, Andrew T.
Flak, Jonathan N.
Johnson, Travis S.
author_facet Lin, Li
Basu, Rashmita
Chatterjee, Debolina
Templin, Andrew T.
Flak, Jonathan N.
Johnson, Travis S.
author_sort Lin, Li
collection PubMed
description High-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.
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spelling pubmed-104126272023-08-11 Disease-associated astrocytes and microglia markers are upregulated in mice fed high fat diet Lin, Li Basu, Rashmita Chatterjee, Debolina Templin, Andrew T. Flak, Jonathan N. Johnson, Travis S. Sci Rep Article High-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. Nature Publishing Group UK 2023-08-09 /pmc/articles/PMC10412627/ /pubmed/37558676 http://dx.doi.org/10.1038/s41598-023-39890-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lin, Li
Basu, Rashmita
Chatterjee, Debolina
Templin, Andrew T.
Flak, Jonathan N.
Johnson, Travis S.
Disease-associated astrocytes and microglia markers are upregulated in mice fed high fat diet
title Disease-associated astrocytes and microglia markers are upregulated in mice fed high fat diet
title_full Disease-associated astrocytes and microglia markers are upregulated in mice fed high fat diet
title_fullStr Disease-associated astrocytes and microglia markers are upregulated in mice fed high fat diet
title_full_unstemmed Disease-associated astrocytes and microglia markers are upregulated in mice fed high fat diet
title_short Disease-associated astrocytes and microglia markers are upregulated in mice fed high fat diet
title_sort disease-associated astrocytes and microglia markers are upregulated in mice fed high fat diet
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10412627/
https://www.ncbi.nlm.nih.gov/pubmed/37558676
http://dx.doi.org/10.1038/s41598-023-39890-0
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