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dc.contributor.authorHans, Sakshi
dc.contributor.authorStanton, Janelle E.
dc.contributor.authorSauer, Ann Katrin
dc.contributor.authorShiels, Katie
dc.contributor.authorSaha, Sushanta Kumar
dc.contributor.authorLordan, Ronan
dc.contributor.authorTsoupras, Alexandros
dc.contributor.authorZabetakis, Ioannis
dc.contributor.authorGrabrucker, Andreas M.
dc.date.accessioned2024-10-16T10:57:52Z
dc.date.available2024-10-16T10:57:52Z
dc.date.copyright2024
dc.date.issued2024-04-20
dc.identifier.citationHans, S., Stanton, J. E., Sauer, A. K., Shiels, K., Saha, S. K., Lordan, R., Tsoupras, A., Zabetakis, I. and Grabrucker, A. M. (2024) Polar lipids modify Alzheimer’s Disease pathology by reducing astrocyte pro-inflammatory signaling through platelet-activating factor receptor (PTAFR) modulation. Lipids in Health and Disease, 23(113). https://doi.org/ 10.1186/s12944-024-02106-zen_US
dc.identifier.urihttps://research.thea.ie/handle/20.500.12065/4844
dc.description.abstractBackground: Pro-inflammatory processes triggered by the accumulation of extracellular amyloid beta (Aβ) peptides are a well-described pathology in Alzheimer’s disease (AD). Activated astrocytes surrounding Aβ plaques contribute to inflammation by secreting proinflammatory factors. While astrocytes may phagocytize Aβ and contribute to Aβ clearance, reactive astrocytes may also increase Aβ production. Therefore, identifying factors that can attenuate astrocyte activation and neuroinflammation and how these factors influence pro-inflammatory pathways is important for developing therapeutic and preventive strategies in AD. Here, we identify the platelet-activating factor receptor (PTAFR) pathway as a key mediator of astrocyte activation. Intriguingly, several polar lipids (PLs) have exhibited anti inflammatory protective properties outside the central nervous system through their inhibitory effect on the PTAFR pathway. Thus, we additionally investigated whether different PLs also exert inhibitory effects on the PAF pathway in astrocytes and whether their presence influences astrocytic pro-inflammatory signalling and known AD pathologies in vitro. Methods: PLs from salmon and yogurt were extracted using novel food-grade techniques and their fatty acid profile was determined using LC/MS. The effect of PLs on parameters such as astrocyte activation and generation of oxygen species (ROS) was assessed. Additionally, effects of the secretome of astrocytes treated with these polar lipids on aged neurons was measured. Results: We show that PLs obtained from salmon and yogurt lower astrocyte activation, the generation of reactive oxygen species (ROS), and extracellular Aβ accumulation. Cell health of neurons exposed to the secretome of astrocytes treated with salmon-derived PLs and Aβ was less affected than those treated with astrocytes exposed to Aβ only. Conclusion: Our results highlight a novel underlying mechanism, why consuming PL-rich foods such as fish and dairy may reduce the risk of developing dementia and associated disorders.en_US
dc.publisherBioMed Central Ltden_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subjectPola lipidsen_US
dc.subjectAlzheimer's Diseaseen_US
dc.subjectBeta-amyloiden_US
dc.subjectNeuroinflammationen_US
dc.subjectNutritionen_US
dc.subjectAstrocytesen_US
dc.subjectGlial cellsen_US
dc.titlePolar lipids modify Alzheimer’s Disease pathology by reducing astrocyte pro-inflammatory signaling through platelet-activating factor receptor (PTAFR) modulationen_US
dc.contributor.affiliationShannon Applied Biotechnology Centre, Technological University of the Shannon, Moylish Parken_US
dc.description.peerreviewyesen_US
dc.identifier.doi10.1186/s12944-024-02106-zen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-1603-8882en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-3981-8833en_US
dc.rights.accessrightsinfo:eu-repo/semantics/openAccessen_US
dc.subject.departmentShannon Applied Biotechnology Centre, Technological University of the Shannon, Moylish Parken_US


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Attribution 3.0 United States
Except where otherwise noted, this item's license is described as Attribution 3.0 United States