The chemokine CCL5 induces selective migration of bovine classical monocytes and drives their differentiation into LPS-hyporesponsive macrophages in vitro

Dev Comp Immunol. 2014 Dec;47(2):169-77. doi: 10.1016/j.dci.2014.07.014. Epub 2014 Jul 23.

Abstract

Human and mouse studies indicate distinct roles of selected chemokines for monocyte subset attraction. We therefore analyzed the still unknown sensitivity and response of bovine monocyte subsets toward two monocyte-attracting chemokines (CCL2, CCL5). Only CCL5 induced a significant Ca(2+)influx and migration response in bovine monocytes, with classical and intermediate monocytes being significantly stimulated and attracted compared to nonclassical monocytes. The presence of CCL5 during in vitro macrophage differentiation did not alter their capacity to phagocytize or to generate reactive oxygen species upon stimulation with E. coli. However, macrophages differentiated in the presence of CCL5 displayed an altered phenotype with significantly less expressed CD14 and MHC class II molecules, whereas CD16 was upregulated. Moreover, CCL5-differentiated macrophages displayed a reduced upregulation of CXCL8, ARG1, IL6 and IL10 mRNA. Taken together, CCL5 but not CCL2 mainly attract bovine classical monocytes and promote their differentiation into LPS-hypo-responsive macrophages.

Keywords: Cattle; Chemokine; Macrophage; Monocyte.

MeSH terms

  • Animals
  • Arginase / genetics
  • Arginase / immunology
  • Calcium / metabolism
  • Cattle
  • Cell Differentiation / drug effects
  • Chemokine CCL2 / pharmacology
  • Chemokine CCL5 / pharmacology*
  • Chemotaxis / drug effects*
  • Escherichia coli / immunology
  • Female
  • Gene Expression Regulation
  • Interleukin-10 / genetics
  • Interleukin-10 / immunology
  • Interleukin-6 / genetics
  • Interleukin-6 / immunology
  • Interleukin-8 / genetics
  • Interleukin-8 / immunology
  • Ion Transport / drug effects
  • Lipopolysaccharide Receptors / genetics
  • Lipopolysaccharide Receptors / immunology
  • Lipopolysaccharides / pharmacology*
  • Macrophages / drug effects*
  • Macrophages / immunology
  • Macrophages / metabolism
  • Monocytes / drug effects*
  • Monocytes / immunology
  • Monocytes / metabolism
  • Phagocytosis / drug effects
  • Primary Cell Culture
  • Reactive Oxygen Species / metabolism
  • Receptors, IgG / genetics
  • Receptors, IgG / immunology

Substances

  • Chemokine CCL2
  • Chemokine CCL5
  • Interleukin-6
  • Interleukin-8
  • Lipopolysaccharide Receptors
  • Lipopolysaccharides
  • Reactive Oxygen Species
  • Receptors, IgG
  • Interleukin-10
  • Arginase
  • Calcium