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    <link>https://hdl.handle.net/10216/26155</link>
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        <rdf:li rdf:resource="https://hdl.handle.net/10216/149489" />
        <rdf:li rdf:resource="https://hdl.handle.net/10216/125615" />
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    <dc:date>2026-07-18T07:16:10Z</dc:date>
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  <item rdf:about="https://hdl.handle.net/10216/149489">
    <title>Dectin-1-Mediated Production of Pro-Inflammatory Cytokines Induced by Yeast β-Glucans in Bovine Monocytes</title>
    <link>https://hdl.handle.net/10216/149489</link>
    <description>Title: Dectin-1-Mediated Production of Pro-Inflammatory Cytokines Induced by Yeast β-Glucans in Bovine Monocytes
Abstract: Yeast-derived products containing β-glucans have long been used as feed supplements in domesticated animals in an attempt to increase immunity. β-glucans are mainly recognized by the cell surface receptor CLEC7A, also designated Dectin-1. Although the immune mechanisms elicited through Dectin-1 activation have been studied in detail in mice and humans, they are poorly understood in other species. Here, we evaluated the response of bovine monocytes to soluble and particulate purified β-glucans, and also to Zymosan. Our results show that particulate, but not soluble β-glucans, can upregulate the surface expression of costimulatory molecules CD80 and CD86 on bovine monocytes. In addition, stimulated cells increased production of IL-8 and of TNF, IL1B, and IL6 mRNA expression, in a dose-dependent manner, which correlated positively with CLEC7A gene expression. Production of IL-8 and TNF expression decreased significantly after CLEC7A knockdown using two different pairs of siRNAs. Overall, we demonstrated here that bovine monocytes respond to particulate β-glucans, through Dectin-1, by increasing the expression of pro-inflammatory cytokines. Our data support further studies in cattle on the induction of trained immunity using dietary β-glucans.</description>
    <dc:date>2021-01-01T00:00:00Z</dc:date>
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  <item rdf:about="https://hdl.handle.net/10216/125615">
    <title>Tissue response to neural implants: the use of model systems towards new design solutions of implantable microelectrodes</title>
    <link>https://hdl.handle.net/10216/125615</link>
    <description>Title: Tissue response to neural implants: the use of model systems towards new design solutions of implantable microelectrodes</description>
    <dc:date>2019-08-01T00:00:00Z</dc:date>
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