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  <title>DSpace Collection:</title>
  <link rel="alternate" href="https://hdl.handle.net/10216/26155" />
  <subtitle />
  <id>https://hdl.handle.net/10216/26155</id>
  <updated>2026-07-18T07:16:29Z</updated>
  <dc:date>2026-07-18T07:16:29Z</dc:date>
  <entry>
    <title>Dectin-1-Mediated Production of Pro-Inflammatory Cytokines Induced by Yeast β-Glucans in Bovine Monocytes</title>
    <link rel="alternate" href="https://hdl.handle.net/10216/149489" />
    <author>
      <name />
    </author>
    <id>https://hdl.handle.net/10216/149489</id>
    <updated>2023-05-24T06:28:06Z</updated>
    <published>2021-01-01T00:00:00Z</published>
    <summary type="text">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.</summary>
    <dc:date>2021-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Tissue response to neural implants: the use of model systems towards new design solutions of implantable microelectrodes</title>
    <link rel="alternate" href="https://hdl.handle.net/10216/125615" />
    <author>
      <name />
    </author>
    <id>https://hdl.handle.net/10216/125615</id>
    <updated>2020-01-24T15:59:31Z</updated>
    <published>2019-08-01T00:00:00Z</published>
    <summary type="text">Title: Tissue response to neural implants: the use of model systems towards new design solutions of implantable microelectrodes</summary>
    <dc:date>2019-08-01T00:00:00Z</dc:date>
  </entry>
</feed>

