Frontiers in Immunology (Feb 2024)

Extracellular vesicles released by microglia and macrophages carry endocannabinoids which foster oligodendrocyte differentiation

  • Marta Lombardi,
  • Marta Lombardi,
  • Federica Scaroni,
  • Martina Gabrielli,
  • Martina Gabrielli,
  • Stefano Raffaele,
  • Elisabetta Bonfanti,
  • Fabia Filipello,
  • Paola Giussani,
  • Silvia Picciolini,
  • Nicole Kerlero de Rosbo,
  • Nicole Kerlero de Rosbo,
  • Antonio Uccelli,
  • Antonio Uccelli,
  • Maria Teresa Golia,
  • Maria Teresa Golia,
  • Giulia D’Arrigo,
  • Giulia D’Arrigo,
  • Tiziana Rubino,
  • Kourosh Hooshmand,
  • Cristina Legido-Quigley,
  • Cristina Legido-Quigley,
  • Chiara Fenoglio,
  • Chiara Fenoglio,
  • Alice Gualerzi,
  • Marta Fumagalli,
  • Claudia Verderio,
  • Claudia Verderio

DOI
https://doi.org/10.3389/fimmu.2024.1331210
Journal volume & issue
Vol. 15

Abstract

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IntroductionMicroglia and macrophages can influence the evolution of myelin lesions through the production of extracellular vesicles (EVs). While microglial EVs promote in vitro differentiation of oligodendrocyte precursor cells (OPCs), whether EVs derived from macrophages aid or limit OPC maturation is unknown.MethodsImmunofluorescence analysis for the myelin protein MBP was employed to evaluate the impact of EVs from primary rat macrophages on cultured OPC differentiation. Raman spectroscopy and liquid chromatography-mass spectrometry was used to define the promyelinating lipid components of myelin EVs obtained in vitro and isolated from human plasma.Results and discussionHere we show that macrophage-derived EVs do not promote OPC differentiation, and those released from macrophages polarized towards an inflammatory state inhibit OPC maturation. However, their lipid cargo promotes OPC maturation in a similar manner to microglial EVs. We identify the promyelinating endocannabinoids anandamide and 2-arachidonoylglycerol in EVs released by both macrophages and microglia in vitro and circulating in human plasma. Analysis of OPC differentiation in the presence of the endocannabinoid receptor antagonists SR141716A and AM630 reveals a key role of vesicular endocannabinoids in OPC maturation. From this study, EV-associated endocannabinoids emerge as important mediators in microglia/macrophage-oligodendrocyte crosstalk, which may be exploited to enhance myelin repair.

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