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dc.contributor.authorMurphy, Emma J.
dc.contributor.authorRezoagli, Emanuele
dc.contributor.authorPogue, Robert
dc.contributor.authorSimonassi-Paiva, Bianca
dc.contributor.authorAbidin, Ismin Izwani Zainol
dc.contributor.authorFehrenbach, Gustavo Waltzer
dc.contributor.authorO'Neil, Emer
dc.contributor.authorMajor, Ian
dc.contributor.authorLaffey, John G.
dc.contributor.authorRowan, Neil J.
dc.date.accessioned2021-12-16T20:39:36Z
dc.date.available2021-12-16T20:39:36Z
dc.date.copyright2022
dc.date.issued2022-02-25
dc.identifier.citationMurphy, E.J., Rezoagli,E. Pogue,R., Simonassi-Paiva,B., Abidin,I.I.Z., Fehrenbach, G.W., O'Neill, E., Major, I., Laffey, J., Rowan, N., (2022) Immunomodulatory activity of β-glucan polysaccharides isolated from different species of mushroom – A potential treatment for inflammatory lung conditions, Science of The Total Environment, 809 152177, , https://doi.org/10.1016/j.scitotenv.2021.en_US
dc.identifier.isbn0048-9697
dc.identifier.urihttp://research.thea.ie/handle/20.500.12065/3870
dc.description.abstractAcute respiratory distress syndrome (ARDS) is the most common form of acute severe hypoxemic respiratory failure in the critically ill with a hospital mortality of 40%. Alveolar inflammation is one of the hallmarks for this disease. β-Glucans are polysaccharides isolated from a variety of natural sources including mushrooms, with documented immune modulating properties. To investigate the immunomodulatory activity of β-glucans and their potential as a treatment for ARDS, we isolated and measured glucan-rich polysaccharides from seven species of mushrooms. We used three models of in-vitro injury in THP-1 macrophages, Peripheral blood mononuclear cells (CD14+) (PMBCs) isolated from healthy volunteers and lung epithelial cell lines. We observed variance between β-glucan content in extracts isolated from seven mushroom species. The extracts with the highest β-glucan content found was Lentinus edodes which contained 70% w/w and Hypsizygus tessellatus which contained 80% w/w with low levels of α-glucan. The extracts had the ability to induce secretion of up to 4000 pg/mL of the inflammatory cytokine IL-6, and up to 5000 pg/mL and 500 pg/mL of the anti-inflammatory cytokines IL-22 and IL-10, respectively, at a concentration of 1 mg/mL in THP-1 macrophages. In the presence of cytokine injury, IL-8 was reduced from 15,000 pg/mL to as low as 10,000 pg/mL in THP-1 macrophages. After insult with LPS, phagocytosis dropped from 70–90% to as low 10% in CD14+ PBMCs. After LPS insult CCL8 relative gene expression was reduced, and IL-10 relative gene expression increased from 50 to 250-fold in THP-1 macrophages. In lung epithelial cells, both A549 and BEAS-2B after IL-1β insult, IL-8 levels dropped from 10,000 pg/mL to as low as 6000 pg/mL. TNF-α levels dropped 10-fold from 100 pg/mL to just below 10 pg/mL. These results demonstrate the therapeutic potential of β-glucans in inflammatory lung conditions. Findings also advance bio-based research that connects green innovation with One Health applications for the betterment of society.en_US
dc.formatPDFen_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.ispartofScience of the Total Environmenten_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectβ-Glucansen_US
dc.subjectTHP-1 macrophagesen_US
dc.subjectLung injuryen_US
dc.subjectARDSen_US
dc.subjectMedicinal mushroomsen_US
dc.subjectOne-healthen_US
dc.titleImmunomodulatory activity of β-glucan polysaccharides isolated from different species of mushroom – A potential treatment for inflammatory lung conditionsen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.contributor.affiliationAthlone Institute of Technologyen_US
dc.description.peerreviewyesen_US
dc.identifier.doi10.1016/j.scitotenv.2021.en_US
dc.identifier.orcidhttps://orcid.org/ 0000-0002-5620-0058en_US
dc.identifier.orcidhttps://orcid.org/ 0000-0003-1344-6354en_US
dc.identifier.orcidhttps://orcid.org/ 0000-0003-1228-3733en_US
dc.identifier.orcidhttps://orcid.org/ 0000-0002-0538-9786en_US
dc.rights.accessrightsinfo:eu-repo/semantics/openAccessen_US
dc.subject.departmentBioscience Research Institute AITen_US
dc.type.versioninfo:eu-repo/semantics/submittedVersionen_US


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Attribution-NonCommercial-NoDerivatives 4.0 International
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