Dectin-1-Mediated Production of Pro-Inflammatory Cytokines Induced by Yeast β-Glucans in Bovine Monocytes

Front Immunol. 2021 May 28:12:689879. doi: 10.3389/fimmu.2021.689879. eCollection 2021.

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.

Keywords: CLEC7A; bovine; cytokines; dectin-1; monocytes; siRNA; β-glucans.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Cells, Cultured
  • Cytokines / genetics
  • Cytokines / metabolism*
  • Inflammation Mediators / metabolism*
  • Lectins, C-Type / genetics
  • Lectins, C-Type / metabolism*
  • Lipopolysaccharide Receptors / metabolism
  • Monocytes / drug effects*
  • Monocytes / immunology
  • Monocytes / metabolism
  • Saccharomyces cerevisiae / metabolism*
  • Up-Regulation
  • beta-Glucans / metabolism
  • beta-Glucans / pharmacology*

Substances

  • CLEC7A protein, human
  • Cytokines
  • Inflammation Mediators
  • Lectins, C-Type
  • Lipopolysaccharide Receptors
  • beta-Glucans
  • dectin 1
  • beta-1,3-glucan