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    <subfield code="a">10.3389/fnut.2023.1287312</subfield>
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    <subfield code="2">sideral</subfield>
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    <subfield code="a">ART-2023-136323</subfield>
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    <subfield code="a">eng</subfield>
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    <subfield code="a">Díez-Sainz, Ester</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">miR482f and miR482c-5p from edible plant-derived foods inhibit the expression of pro-inflammatory genes in human THP-1 macrophages</subfield>
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  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2023</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
    <subfield code="f">Unrestricted</subfield>
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    <subfield code="a">Edible plants can exert anti-inflammatory activities in humans, being potentially useful in the treatment of inflammatory diseases. Plant-derived microRNAs have emerged as cross-kingdom gene expression regulators and could act as bioactive molecules involved in the beneficial effects of some edible plants. We investigated the role of edible plant-derived microRNAs in the modulation of pro-inflammatory human genes.MethodsMicroRNAs from plant-derived foods were identified by next-generation sequencing. MicroRNAs with inflammatory putative targets were selected, after performing in silico analyses. The expression of candidate plant-derived miRNAs was analyzed by qPCR in edible plant-derived foods and their effects were evaluated in THP-1 monocytes differentiated to macrophages. The bioavailability of candidate plant miRNAs in humans was evaluated in feces and serum samples by qPCR.ResultsmiR482f and miR482c-5p are present in several edible plant-derived foods, such as fruits, vegetables, and cooked legumes and cereals, and fats and oils. Transfections with miR482f and miR482c-5p mimics decreased the gene expression of CLEC7A and NFAM1, and TRL6, respectively, in human THP-1 monocytes differentiated to macrophages, which had an impact on gene expression profile of inflammatory biomarkers. Both microRNAs (miR482f and miR482c-5p) resisted degradation during digestion and were detected in human feces, although not in serum.ConclusionOur findings suggest that miR482f and miR482c-5p can promote an anti-inflammatory gene expression profile in human macrophages in vitro and their bioavailability in humans can be achieved through diet, but eventually restricted at the gut level.</subfield>
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    <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/RTI2018-102205-B-I00</subfield>
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    <subfield code="a">NUTRITION &amp; DIETETICS</subfield>
    <subfield code="b">31 / 114 = 0.272</subfield>
    <subfield code="c">2023</subfield>
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  <datafield tag="593" ind1=" " ind2=" ">
    <subfield code="a">Food Science</subfield>
    <subfield code="c">2023</subfield>
    <subfield code="d">Q1</subfield>
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    <subfield code="a">Nutrition and Dietetics</subfield>
    <subfield code="c">2023</subfield>
    <subfield code="d">Q2</subfield>
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    <subfield code="a">Endocrinology, Diabetes and Metabolism</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Lorente-Cebrián, Silvia</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-1033-6152</subfield>
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    <subfield code="a">Aranaz, Paula</subfield>
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    <subfield code="a">Amri, Ez-Zoubir</subfield>
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    <subfield code="a">Riezu-Boj, José I.</subfield>
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    <subfield code="a">Milagro, Fermín I.</subfield>
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    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Farmac.Fisiol.y Med.L.F.</subfield>
    <subfield code="c">Área Fisiología</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">10 (2023), 1287312 [15 pp.]</subfield>
    <subfield code="p">Front. Nutr.</subfield>
    <subfield code="t">Frontiers in Nutrition</subfield>
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