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GEO help: Mouse over screen elements for information. |
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Status |
Public on Feb 25, 2021 |
Title |
Microglia use TAM receptors to detect and engulf amyloid beta plaques |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Two microglial TAM receptor tyrosine kinases - Axl and Mer - have been linked to Alzheimer’s disease, but their roles in disease have not been tested experimentally. We find that in Alzheimer’s disease and its mouse models, induced expression of Axl and Mer in amyloid plaque-associated microglia is coupled to induced plaque decoration by the TAM ligand Gas6 and its co-ligand phosphatidylserine. In the APP/PS1 mouse model of Alzheimer’s disease, sIngle cell RNAseq analysis comparing wild type microglia with those with Axl and Mer deficiency reveals a similar disease state transitional program of microglia but a dampened differential expression of numerous AD siganture genes in microglia lacking TAM receptors. In line with the transcriptomic data, using two-photon microscopy, we show that genetic ablation of Axl and Mer results in microglia that are unable to normally detect, respond to, organize, or phagocytose amyloid beta plaques. These major deficits notwithstanding, and contrary to expectation, TAM-deficient APP/PS1 mice develop fewer dense-core plaques than APP/PS1 mice with normal microglia. Our findings reveal that the TAM system is an essential mediator of microglial recognition and engulfment of amyloid plaques, and that TAM-driven microglial phagocytosis does not constrain, but rather promotes, plaque development.
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Overall design |
Immune cells were isolated and sorted from pooled cortices (2 per sample) from 18 month old APP/PS1 (AD) and age-matched APP/PS1 Axl-/- Mertk-/- mice (ADAM), 2 biological replicates per group in total of 4 samples.
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Contributor(s) |
Huang Y, Happonen K, Lemke G, Huang L, Nimmerjahn A, Burrola P |
Citation(s) |
33859405 |
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Submission date |
Oct 30, 2020 |
Last update date |
Mar 28, 2022 |
Contact name |
April Elizabeth Williams |
E-mail(s) |
apriljack06@gmail.com, awilliams@salk.edu
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Phone |
7345461645
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Organization name |
Salk Institute for Biological Studies
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Department |
IGC
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Street address |
10010 N Torrey Pines Rd
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City |
San Diego |
State/province |
California |
ZIP/Postal code |
92037 |
Country |
USA |
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Platforms (1) |
GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
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Samples (4)
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Relations |
BioProject |
PRJNA673444 |
SRA |
SRP290191 |
Supplementary file |
Size |
Download |
File type/resource |
GSE160523_meta_data.tsv.gz |
915.2 Kb |
(ftp)(http) |
TSV |
GSE160523_rawCount.tsv.gz |
30.1 Mb |
(ftp)(http) |
TSV |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
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