4.7 Article

Receptor-heteromer mediated regulation of endocannabinoid signaling in activated microglia. Role of CB1 and CB2 receptors and relevance for Alzheimer's disease and levodopa-induced dyskinesia

Journal

BRAIN BEHAVIOR AND IMMUNITY
Volume 67, Issue -, Pages 139-151

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbi.2017.08.015

Keywords

Endocannabinoid; Heterodimers; Heteromers; G-protein-coupled receptor; GPCR; GPCR heteromer

Funding

  1. Spanish Ministry of Economy and Competitiveness (MINECO) [BFU2012-37907, SAF2012-39875-C02-01]
  2. EU FEDER
  3. Fundacio La Marato de TV3 [201413330, 201441331]

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Endocannabinoids are important regulators of neurotransmission and, acting on activated microglia, they are postulated as neuroprotective agents. Endocannabinoid action is mediated by CB1 and CB2 receptors, which may form heteromeric complexes (CB1-CB(2)Hets) with unknown function in microglia. We aimed at establishing the expression and signaling properties of cannabinoid receptors in resting and LPS/IFN-gamma-activated microglia. In activated microglia mRNA transcripts increased (2 fold for CB1 and circa 20 fold for CB2), whereas receptor levels were similar for CB1 and markedly upregulated for CB2; CB1-CB(2)Hets were also upregulated. Unlike in resting cells, CB2 receptors became robustly coupled to GI in activated cells, in which CB1-CB(2)Hets mediated a potentiation effect. Hence, resting cells were refractory while activated cells were highly responsive to cannabinoids. Interestingly, similar results were obtained in cultures treated with E-amyloid (A beta(1-42)). Microglial activation markers were detected in the striatum of a Parkinson's disease (PD) model and, remarkably, in primary microglia cultures from the hippocampus of mutant beta-amyloid precursor protein (APP(sw,Ind)) mice, a transgenic Alzheimer's disease (AD) model. Also of note was the similar cannabinoid receptor signaling found in primary cultures of microglia from APP(sw,Ind) and in cells from control animals activated using LPS plus IFN-gamma. Expression of CB1-CB(2)Hets was increased in the striatum from rats rendered dyskinetic by chronic levodopa treatment. In summary, our results showed sensitivity of activated microglial cells to cannabinoids, increased CB1-CB(2)Het expression in activated microglia and in microglia from the hippocampus of an AD model, and a correlation between levodopa-induced dyskinesia and striatal microglial activation in a PD model. Cannabinoid receptors and the CB1-CB2 heteroreceptor complex in activated microglia have potential as targets in the treatment of neurodegenerative diseases. (C) 2017 Elsevier Inc. All rights reserved.

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