Endocannabinoid content in fetal bovine sera - unexpected effects on mononuclear cells and osteoclastogenesis

J Immunol Methods. 2011 Oct 28;373(1-2):219-28. doi: 10.1016/j.jim.2011.08.021. Epub 2011 Sep 3.

Abstract

The major endocannabinoids (ECs) arachidonoylethanolamide (AEA) and 2-arachidonoylglycerol (2-AG) and related N-ethanolamines act as full and partial agonists at CB(1), CB(2), GPR55, PPAR and TRPV1 receptors to various degrees. These receptors are also expressed in immune cells like monocytes/macrophages where they regulate different cellular processes. In this study, potentially bioactive lipids in fetal bovine sera (FBS) were quantified by GC/MS. We found that several commercial FBS contain ECs and bioactive amounts of 2-AG (250-700 nM). We show that residual 2-AG from FBS can activate primary macrophages and increase migration and RANKL-stimulated osteoclastogenesis. Furthermore, 2-AG high-content sera specifically upregulated LPS-stimulated IL-6 expression in U937 cells. Polymyxin B beads may be used to selectively and efficiently remove 2-AG from sera, but not arachidonic acid and N-ethanolamines. In conclusion, 2-AG in cell culture media may significantly influence cellular experiments. CD14+ mononuclear cells which strongly express surface CB receptors may be particularly sensitive towards residual 2-AG from FBS. Therefore, the EC content in culture media should be controlled in biological experiments involving monocytes/macrophages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arachidonic Acids / metabolism
  • Arachidonic Acids / pharmacology
  • Cannabinoid Receptor Modulators / metabolism*
  • Cannabinoid Receptor Modulators / pharmacology*
  • Cattle
  • Cell Movement / drug effects
  • Cells, Cultured
  • Endocannabinoids*
  • Fetal Blood / chemistry*
  • Flow Cytometry
  • Gas Chromatography-Mass Spectrometry
  • Glycerides / metabolism
  • Glycerides / pharmacology
  • Humans
  • Interleukin-6 / metabolism
  • Lipids / analysis
  • Lipids / isolation & purification
  • Lipopolysaccharide Receptors / metabolism
  • Lipopolysaccharides / pharmacology
  • Macrophage Activation / drug effects
  • Macrophages / cytology
  • Macrophages / drug effects*
  • Macrophages / metabolism
  • Monocytes / cytology
  • Monocytes / drug effects*
  • Monocytes / metabolism
  • Osteoclasts / cytology
  • Osteoclasts / drug effects*
  • Osteoclasts / metabolism
  • RANK Ligand / pharmacology
  • Receptors, Cannabinoid / metabolism
  • U937 Cells

Substances

  • Arachidonic Acids
  • Cannabinoid Receptor Modulators
  • Endocannabinoids
  • Glycerides
  • Interleukin-6
  • Lipids
  • Lipopolysaccharide Receptors
  • Lipopolysaccharides
  • RANK Ligand
  • Receptors, Cannabinoid
  • glyceryl 2-arachidonate