{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"submitter":["Makarava N"],"funding":["National Institute of Health","NINDS NIH HHS"],"pubmed_abstract":["Microglia are recognized as the main cells in the central nervous system responsible for phagocytosis. The current study demonstrated that in prion disease, microglia effectively phagocytose prions or PrPSc during early preclinical stages. However, a critical shift occured in microglial activity during the late preclinical stage, transitioning from PrPSc uptake to establishing extensive neuron-microglia body-to-body cell contacts. This change was followed by a rapid accumulation of PrPSc in the brain. Microglia that enveloped neurons exhibited hypertrophic, cathepsin D-positive lysosomal compartments. However, most neurons undergoing envelopment were only partially encircled by microglia. Despite up to 40% of cortical neurons being partially enveloped at clinical stages, only a small perce"],"journal":["The Journal of clinical investigation"],"pagination":["e181169"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11601909"],"repository":["biostudies-literature"],"pubmed_title":["Reactive microglia partially envelop viable neurons in prion diseases."],"pmcid":["PMC11601909"],"funding_grant_id":["R01 NS045585","NS045585","R01 NS110630","NS129502","NS110630","R01 NS129502"],"pubmed_authors":["Safadi T","Bocharova O","Pandit NP","Baiardi S","Parchi P","Molesworth K","Makarava N","Zhang L","Mychko O","Baskakov IV"],"additional_accession":[]},"is_claimable":false,"name":"Reactive microglia partially envelop viable neurons in prion diseases.","description":"Microglia are recognized as the main cells in the central nervous system responsible for phagocytosis. The current study demonstrated that in prion disease, microglia effectively phagocytose prions or PrPSc during early preclinical stages. However, a critical shift occured in microglial activity during the late preclinical stage, transitioning from PrPSc uptake to establishing extensive neuron-microglia body-to-body cell contacts. This change was followed by a rapid accumulation of PrPSc in the brain. Microglia that enveloped neurons exhibited hypertrophic, cathepsin D-positive lysosomal compartments. However, most neurons undergoing envelopment were only partially encircled by microglia. Despite up to 40% of cortical neurons being partially enveloped at clinical stages, only a small perce","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Oct","modification":"2025-04-19T17:35:34Z","creation":"2025-04-19T17:35:34Z"},"accession":"S-EPMC11601909","cross_references":{"pubmed":["39361421"],"doi":["10.1172/JCI181169"]}}