{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Gaunt JR"],"funding":["NIDDK NIH HHS","Ministry of Education - Singapore","NINDS NIH HHS","National Institutes of Health","NIH HHS"],"pagination":["269"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10656954"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["20(1)"],"pubmed_abstract":["Alzheimer's disease (AD) pathology and amyloid-beta (Aβ) plaque deposition progress slowly in the cerebellum compared to other brain regions, while the entorhinal cortex (EC) is one of the most vulnerable regions. Using a knock-in AD mouse model (App KI), we show that within the cerebellum, the deep cerebellar nuclei (DCN) has particularly low accumulation of Aβ plaques. To identify factors that might underlie differences in the progression of AD-associated neuropathology across regions, we profiled gene expression in single nuclei (snRNAseq) across all cell types in the DCN and EC of wild-type (WT) and App KI male mice at age 7 months. We found differences in expression of genes associated with inflammatory activation, PI3K-AKT signalling, and neuron support functions between both regions"],"journal":["Journal of neuroinflammation"],"pubmed_title":["Cytokine enrichment in deep cerebellar nuclei is contributed by multiple glial populations and linked to reduced amyloid plaque pathology."],"pmcid":["PMC10656954"],"funding_grant_id":["MOE2017-T3-1-002","R01 DK124801","R01DK124801","R01 NS124844"],"pubmed_authors":["Yip AKK","Chen AI","Zainolabidin N","Tan JM","Ch'ng TH","Gaunt JR","Low AYT"],"additional_accession":[]},"is_claimable":false,"name":"Cytokine enrichment in deep cerebellar nuclei is contributed by multiple glial populations and linked to reduced amyloid plaque pathology.","description":"Alzheimer's disease (AD) pathology and amyloid-beta (Aβ) plaque deposition progress slowly in the cerebellum compared to other brain regions, while the entorhinal cortex (EC) is one of the most vulnerable regions. Using a knock-in AD mouse model (App KI), we show that within the cerebellum, the deep cerebellar nuclei (DCN) has particularly low accumulation of Aβ plaques. To identify factors that might underlie differences in the progression of AD-associated neuropathology across regions, we profiled gene expression in single nuclei (snRNAseq) across all cell types in the DCN and EC of wild-type (WT) and App KI male mice at age 7 months. We found differences in expression of genes associated with inflammatory activation, PI3K-AKT signalling, and neuron support functions between both regions","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 Nov","modification":"2026-05-29T08:08:54.753Z","creation":"2024-11-15T18:23:04.784Z"},"accession":"S-EPMC10656954","cross_references":{"pubmed":["37978387"],"doi":["10.1186/s12974-023-02913-8"]}}