dc.contributor.author | Murphy, Emma J. | |
dc.contributor.author | Rezoagli, Emanuele | |
dc.contributor.author | Pogue, Robert | |
dc.contributor.author | Simonassi-Paiva, Bianca | |
dc.contributor.author | Abidin, Ismin Izwani Zainol | |
dc.contributor.author | Fehrenbach, Gustavo Waltzer | |
dc.contributor.author | O'Neil, Emer | |
dc.contributor.author | Major, Ian | |
dc.contributor.author | Laffey, John G. | |
dc.contributor.author | Rowan, Neil J. | |
dc.date.accessioned | 2021-12-16T20:39:36Z | |
dc.date.available | 2021-12-16T20:39:36Z | |
dc.date.copyright | 2022 | |
dc.date.issued | 2022-02-25 | |
dc.identifier.citation | Murphy, 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.isbn | 0048-9697 | |
dc.identifier.uri | http://research.thea.ie/handle/20.500.12065/3870 | |
dc.description.abstract | Acute 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.format | PDF | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.ispartof | Science of the Total Environment | en_US |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | β-Glucans | en_US |
dc.subject | THP-1 macrophages | en_US |
dc.subject | Lung injury | en_US |
dc.subject | ARDS | en_US |
dc.subject | Medicinal mushrooms | en_US |
dc.subject | One-health | en_US |
dc.title | Immunomodulatory activity of β-glucan polysaccharides isolated from different species of mushroom – A potential treatment for inflammatory lung conditions | en_US |
dc.type | info:eu-repo/semantics/article | en_US |
dc.contributor.affiliation | Athlone Institute of Technology | en_US |
dc.description.peerreview | yes | en_US |
dc.identifier.doi | 10.1016/j.scitotenv.2021. | en_US |
dc.identifier.orcid | https://orcid.org/ 0000-0002-5620-0058 | en_US |
dc.identifier.orcid | https://orcid.org/ 0000-0003-1344-6354 | en_US |
dc.identifier.orcid | https://orcid.org/ 0000-0003-1228-3733 | en_US |
dc.identifier.orcid | https://orcid.org/ 0000-0002-0538-9786 | en_US |
dc.rights.accessrights | info:eu-repo/semantics/openAccess | en_US |
dc.subject.department | Bioscience Research Institute AIT | en_US |
dc.type.version | info:eu-repo/semantics/submittedVersion | en_US |