NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE260461 Query DataSets for GSE260461
Status Public on Jun 04, 2024
Title Sex-dependent APOE4 Neutrophil-microglia interactions drive cognitive impairment in Alzheimer's Disease
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary APOE4 is the strongest genetic risk factor for Alzheimer's disease (AD), with increased odds ratios in females. Targeting amyloid plaques shows modest improvement in male non-APOE4 carriers. Leveraging single-cell transcriptomics across APOE variants in both sexes, multiplex flow cytometry, and validation in two independent cohorts of APOE4 female AD patients, we identify a new subset of neutrophils interacting with microglia associated with cognitive impairment. This phenotype is defined by increased IL-17 and IL-1 co-expressed gene modules in blood neutrophils and in microglia of cognitively impaired female APOE e4 carriers, showing increased infiltration to the AD brain. APOE4 female IL-17+ neutrophils upregulated the immunosuppressive cytokines IL-10 and TGFB and immune checkpoints, including LAG-3 and PD-1, associated with accelerated immune aging. Deletion of APOE4 in neutrophils reduced this immunosuppressive phenotype and restored the microglial response to neurodegeneration (MGnD), limiting plaque pathology in AD mice. Mechanistically, IL-17F upregulated in APOE4 neutrophils interacts with microglial IL-17RA to suppress the induction of MGnD phenotype, and blocking this axis supported cognitive improvement in AD mice. These findings provide a translational basis to target IL-17F in APOE e4 female carriers with cognitive impairment.
 
Overall design Nuclei were isolated from frozen human brain tissue and enriched for microglia and astrocytes using Fluorescence-activated nuclei sorting (FANS) and analysed using snRNAseq. Donors included both males and females from an Alzheimer's diseased (AD) cohort and non-demented control (CTRL) cohort that have the APOE 3/3 or 3/4 genotype
 
Contributor(s) Rosenzweig N, Kleemann KL, Rust T, Grucci M, Aronchik M, Brouwer N, Cooper-Hohn J, Iyer M, Krishnan RK, Valenbreder I, Carpenter M, Kisha S, Chadarevian JP, Brandão W, Yahya T, Durao A, Yin Z, Properzi M, Yang H, Norwaski R, Davtyan H, Blurton-Jones MM, Sperling R, Eggen BJ, Butovsky O
Citation(s) 38961225
Submission date Feb 28, 2024
Last update date Sep 09, 2024
Contact name Neta Rosenzweig
E-mail(s) NROSENZWEIG@BWH.HARVARD.EDU
Organization name Brigham and Women's Hospital, Harvard Medical School
Street address 60 Fenwood Road, 10002K, Brigham and Women’s Hospital
City Boston
State/province Massachusetts
ZIP/Postal code 02115
Country USA
 
Platforms (1)
GPL18573 Illumina NextSeq 500 (Homo sapiens)
Samples (39)
GSM8117703 SPG, AD, APOE3
GSM8117704 SPG, AD, APOE4
GSM8117705 SPG, AD, APOE5
This SubSeries is part of SuperSeries:
GSE243750 SEX-DEPENDENT APOE4 NEUTROPHIL-MICROGLIA INTERACTIONS DRIVE COGNITIVE IMPAIRMENT IN ALZHEIMER'S DISEASE
Relations
BioProject PRJNA1081819

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
GSE260461_RAW.tar 2.0 Gb (http)(custom) TAR (of MTX, TSV)
SRA Run SelectorHelp
Raw data are available in SRA

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