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Identification of Chlamydia pneumoniae and NLRP3 inflammasome activation in Alzheimer’s disease retina

Title: Identification of Chlamydia pneumoniae and NLRP3 inflammasome activation in Alzheimer’s disease retina
Authors: Gaire, Bhakta Prasad; Koronyo, Yosef; Vit, Jean-Philippe; Hutton, Alexandre; Swerdlow, Natalie; Fuchs, Dieu-Trang; Rentsendorj, Altan; Subedi, Lalita; Robinson, Edward; Ljubimov, Alexander V; Schneider, Lon S; Hawes, Debra; Graham, Stuart L; Gupta, Vivek K; Mirzaei, Mehdi; Black, Keith L; Meyer, Jesse G; Arditi, Moshe; Crother, Timothy R; Koronyo-Hamaoui, Maya
Source: Res Sq
Publisher Information: eScholarship, University of California
Publication Year: 2025
Collection: University of California: eScholarship
Subject Terms: 3101 Biochemistry and Cell Biology (for-2020); 31 Biological Sciences (for-2020); Prevention (rcdc); Acquired Cognitive Impairment (rcdc); Infectious Diseases (rcdc); Brain Disorders (rcdc); Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD) (rcdc); Lung (rcdc); Neurodegenerative (rcdc); Eye Disease and Disorders of Vision (rcdc); Neurosciences (rcdc); Aging (rcdc); Pneumonia & Influenza (rcdc); Alzheimer's Disease (rcdc); Dementia (rcdc); Pneumonia (rcdc); 2.1 Biological and endogenous factors (hrcs-rac); Infection (hrcs-hc); Neurological (hrcs-hc); Alzheimer’s disease; Chlamydia pneumoniae (Cp); NLRP3 inflammasome; apoptosis; gliosis; machine learning; retina
Subject Geographic: rs.3.rs - 6658954
Description: Emerging evidence implicates bacterial infections, including Chlamydia pneumoniae (Cp), a gram-negative obligate intracellular bacterium responsible for community-acquired pneumonia, in Alzheimer's disease (AD) pathogenesis. However, the involvement of Cp in early and advanced AD in the retina is unknown. Here, we identified the existence and distribution of intracellular Cp inclusions and related NLRP3 inflammasome activation and neurodegeneration in postmortem retinas and brains from 95 human donors. Histological analysis in neuropathologically-confirmed MCI and AD patients compared with cognitively normal individuals (n=70), revealed 2.9-4.1-fold increases of Cp inclusions in AD retinas and brains, respectively, with no significant increases in MCI retinas or brains. Mass spectrometry-based proteomics in additional cohorts (n=30), revealed dysregulated brain and retinal bacterial infection-related proteins and inflammasome-associated pathways. Retinal Cp was strongly linked to Aβ42, caspase-1 and NLRP3-inflammasome activation components, as well as cleaved caspase-3+ apoptosis and cleaved gasdermin D pyroptotic cell death. Despite increased IBA1+ microgliosis in the AD retina, the Cp-associated microglial population was reduced by 62%, suggesting impaired microglial phagocytosis. Higher retinal Cp burden correlated with APOEε4 status, advanced Braak stage, and cognitive decline. Machine learning models revealed that retinal Cp or NLRP3, in combination with retinal Aβ42, effectively predicted AD diagnosis, Braak stage, and cognition. These findings suggest that Cp infection contributes to AD dementia but is unlikely to initiate AD pathological changes, whereas elevated retinal NLRP3 may serve as an early AD marker. These results underscore the need for future studies investigating Cp's role in AD dementia and testing early antibiotic or inflammasome-targeting therapies.
Document Type: article in journal/newspaper
File Description: application/pdf
Language: unknown
Relation: qt6628w33w; https://escholarship.org/uc/item/6628w33w; https://escholarship.org/content/qt6628w33w/qt6628w33w.pdf
DOI: 10.21203/rs.3.rs-6658954/v1
Availability: https://escholarship.org/uc/item/6628w33w; https://escholarship.org/content/qt6628w33w/qt6628w33w.pdf; https://doi.org/10.21203/rs.3.rs-6658954/v1
Rights: public
Accession Number: edsbas.98CBBBD3
Database: BASE