Resolvin D1 reduces inflammation in co-cultures of primary human macrophages and adipocytes by triggering macrophages

Prostaglandins Leukot Essent Fatty Acids. 2021 Nov:174:102363. doi: 10.1016/j.plefa.2021.102363. Epub 2021 Oct 29.

Abstract

Obesity leads to chronic inflammation of the adipose tissue which is tightly associated with the metabolic syndrome, type 2 diabetes and cardiovascular disease. Inflammation of the adipose tissue is mainly characterized by the presence of crown-like structures composed of inflammatory macrophages in the neighborhood of adipocytes. Resolvin D1 (RvD1), a potent anti-inflammatory and pro-resolving lipid mediator derived from the omega-3 fatty acid docosahexaenoic acid, has been shown to reduce the inflammatory tone of adipose tissue in animal models but the underlying mechanism is not clear. We investigated the effect of RvD1 on the inflammatory state of a human co-culture system of adipocytes and macrophages. For this, human mesenchymal stem cells were differentiated into mature adipocytes and overlaid with human primary macrophages. In this co-culture, 10-500 nM RvD1 dose-dependently reduced the secretion of the pro-inflammatory cytokine IL-6 (-21%) and its soluble receptor IL-6Rα (-22%), of the chemokine MCP-1 (-13%), and of the adipokine leptin (-22%). Similarly, we observed a reduction in secretion of the soluble receptor IL-6Rα (-20%), and TNF-α (-11%) when macrophages alone were treated with RvD1, while no change of cytokine secretion was observed when adipocytes were treated with RvD1. We conclude that RvD1 polarizes macrophages to an anti-inflammatory phenotype, which in turn modulates inflammation in adipocytes.

Keywords: Adipose tissue inflammation; Co-culture; Mesenchymal stem cells; Primary human macrophages; Resolvin D1; Specialized pro-resolving mediators.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / drug effects*
  • Adipocytes / metabolism*
  • Adipose Tissue / metabolism
  • Anti-Inflammatory Agents / pharmacology*
  • Cell Differentiation / physiology
  • Cell Polarity / drug effects
  • Cells, Cultured
  • Coculture Techniques / methods
  • Cytokines / metabolism
  • Docosahexaenoic Acids / pharmacology*
  • Humans
  • Inflammation / drug therapy
  • Inflammation / metabolism
  • Inflammation Mediators / metabolism
  • Leptin / metabolism
  • Macrophages / drug effects*
  • Macrophages / metabolism*
  • Mesenchymal Stem Cells / cytology
  • Obesity / metabolism
  • Phenotype
  • Signal Transduction / drug effects*

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Inflammation Mediators
  • LEP protein, human
  • Leptin
  • resolvin D1
  • Docosahexaenoic Acids