NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE226937 Query DataSets for GSE226937
Status Public on Apr 01, 2024
Title Early amyloid-induced changes in microglia gene expression in APP/PS1 mice [bulk RNA-seq]
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary Alzheimer’s disease (AD) is a progressive neurodegenerative disease and the most common cause of dementia, characterized by deposition of extracellular amyloid-beta (Aβ) aggregates and intraneuronal hyperphosphorylated Tau. Many AD risk genes, identified in genome-wide association studies (GWAS), are expressed in microglia, the innate immune cells of the central nervous system. Specific subtypes of microglia emerged in relation to AD pathology, such as disease-associated microglia (DAMs), which increased in number with age in amyloid mouse models and in human AD cases. However, the initial transcriptional changes in these microglia in response to amyloid are still unknown. Here, to determine early changes in microglia gene expression, hippocampal microglia from APPswe/PS1dE9 (APP/PS1) mice and wildtype littermates were isolated and analyzed by RNA sequencing (RNA-seq). By bulk RNA-seq, transcriptomic changes were detected in hippocampal microglia from 6-months-old APP/PS1 mice. By performing single cell RNA-seq of CD11c-positive and negative microglia from 6-months-old APP/PS1 mice and analysis of the transcriptional trajectory from homeostatic to CD11c-positive microglia, we identified a set of genes that potentally reflect the initial response of microglia to Aβ.
 
Overall design Bulk RNA sequencing analysis of FACS-isolated microglia from hippocampus of APPswe/PSEN1dE9 (APP/PS1, transgenic) and controls at different ages ( 4-, 6-, 9-month-old). N = 3 or 4 per condition.
 
Contributor(s) Oshima T, Kater MS, Huffels CF, Wesseling EM, Middeldorp J, Hol EM, Verheijen MH, Smit AB, Boddeke EW, Eggen BJ
Citation(s) 38515329
Submission date Mar 08, 2023
Last update date May 20, 2024
Contact name Takuya Oshima
E-mail(s) t.oshima@umcg.nl
Organization name University Medical Center Groningen
Department Department of Biomedical Sciences of Cells & Systems
Lab Section Molecular Neurobiology
Street address Antonius Deusinglaan 1
City Groningen
State/province Groningen
ZIP/Postal code 9713AV
Country Netherlands
 
Platforms (1)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
Samples (24)
GSM7088612 App_hip_mic_4m_wt_1
GSM7088613 App_hip_mic_4m_wt_2
GSM7088614 App_hip_mic_4m_wt_3
This SubSeries is part of SuperSeries:
GSE226939 Early amyloid-induced changes in microglia gene expression in APP/PS1 mice
Relations
BioProject PRJNA942288

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE226937_RAW.tar 9.1 Mb (http)(custom) TAR (of TXT)
GSE226937_countmatrix_all_sample.csv.gz 759.6 Kb (ftp)(http) CSV
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap