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• W2919962145 abstract "The purpose of this work was to determine the pro-and anti-inflammatory properties of the single-cell organism Euglena gracilis (EG) and various fractions of its whole biomass.Heterotrophically grown EG was tested, along with its aqueous fraction (E-AQ), the intact linear β-glucan paramylon granules (PAR), and alkaline-solubilized paramylon. Peripheral blood mononuclear cell cultures were treated with the test products and analyzed for a variety of cellular responses. Immune cell activation was evaluated by flow cytometry detection of CD69 levels on CD3-CD56+ NK cells, CD3+CD56+ NKT cells, and monocytes, and cytokines were analyzed from the cell culture supernatants. Antioxidant capacity was measured by Folin-Ciocalteu assay and cellular antioxidant protection and MTT assays.EG and E-AQ were the most effective in driving immune cell responses as measured by CD69 upregulation on NK and NKT cells and proinflammatory (tumor necrosis factor, IL-6, IL-1β) cytokine production. None of the test products effectively stimulated monocyte. EG and PAR inhibited reactive oxygen species under conditions of oxidative stress. E-AQ contained antioxidants capable of providing cellular antioxidant protection from oxidative damage and protection of mitochondrial function under inflammatory conditions.The effects of EG on immune function are only partially attributable to the content of the β-glucan, paramylon. The regulation of additional cellular responses, such a reactive oxygen species production and resistance to oxidative stress, is likely mediated by currently unknown molecules found in the EG cell." @default.
• W2919962145 created "2019-03-11" @default.
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• W2919962145 date "2019-03-01" @default.
• W2919962145 modified "2023-09-26" @default.
• W2919962145 title "<p>Particulate and solubilized &beta;-glucan and non-&beta;-glucan fractions of <em>Euglena gracilis</em> induce pro- and anti-inflammatory innate immune cell responses and exhibit antioxidant properties</p>" @default.
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• W2919962145 doi "https://doi.org/10.2147/jir.s191824" @default.
• W2919962145 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6407518" @default.
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