TY - JOUR
T1 - A mu–delta opioid receptor brain atlas reveals neuronal co-occurrence in subcortical networks
AU - Erbs, Eric
AU - Faget, Lauren
AU - Scherrer, Gregory
AU - Matifas, Audrey
AU - Filliol, Dominique
AU - Vonesch, Jean Luc
AU - Koch, Marc
AU - Kessler, Pascal
AU - Hentsch, Didier
AU - Birling, Marie Christine
AU - Koutsourakis, Manoussos
AU - Vasseur, Laurent
AU - Veinante, Pierre
AU - Kieffer, Brigitte L.
AU - Massotte, Dominique
N1 - Publisher Copyright:
© 2014, The Author(s).
PY - 2015/3
Y1 - 2015/3
N2 - Opioid receptors are G protein-coupled receptors (GPCRs) that modulate brain function at all levels of neural integration, including autonomic, sensory, emotional and cognitive processing. Mu (MOR) and delta (DOR) opioid receptors functionally interact in vivo, but whether interactions occur at circuitry, cellular or molecular levels remains unsolved. To challenge the hypothesis of MOR/DOR heteromerization in the brain, we generated redMOR/greenDOR double knock-in mice and report dual receptor mapping throughout the nervous system. Data are organized as an interactive database offering an opioid receptor atlas with concomitant MOR/DOR visualization at subcellular resolution, accessible online. We also provide co-immunoprecipitation-based evidence for receptor heteromerization in these mice. In the forebrain, MOR and DOR are mainly detected in separate neurons, suggesting system-level interactions in high-order processing. In contrast, neuronal co-localization is detected in subcortical networks essential for survival involved in eating and sexual behaviors or perception and response to aversive stimuli. In addition, potential MOR/DOR intracellular interactions within the nociceptive pathway offer novel therapeutic perspectives.
AB - Opioid receptors are G protein-coupled receptors (GPCRs) that modulate brain function at all levels of neural integration, including autonomic, sensory, emotional and cognitive processing. Mu (MOR) and delta (DOR) opioid receptors functionally interact in vivo, but whether interactions occur at circuitry, cellular or molecular levels remains unsolved. To challenge the hypothesis of MOR/DOR heteromerization in the brain, we generated redMOR/greenDOR double knock-in mice and report dual receptor mapping throughout the nervous system. Data are organized as an interactive database offering an opioid receptor atlas with concomitant MOR/DOR visualization at subcellular resolution, accessible online. We also provide co-immunoprecipitation-based evidence for receptor heteromerization in these mice. In the forebrain, MOR and DOR are mainly detected in separate neurons, suggesting system-level interactions in high-order processing. In contrast, neuronal co-localization is detected in subcortical networks essential for survival involved in eating and sexual behaviors or perception and response to aversive stimuli. In addition, potential MOR/DOR intracellular interactions within the nociceptive pathway offer novel therapeutic perspectives.
KW - Aversive stimuli
KW - Heteromer
KW - Mouse delta opioid receptor
KW - Mouse mu opioid receptor
KW - Receptor brain atlas
KW - mouse data opioid receptor
UR - http://www.scopus.com/inward/record.url?scp=84895775893&partnerID=8YFLogxK
U2 - 10.1007/s00429-014-0717-9
DO - 10.1007/s00429-014-0717-9
M3 - Article
C2 - 24623156
AN - SCOPUS:84895775893
SN - 1863-2653
VL - 220
SP - 677
EP - 702
JO - Brain Structure and Function
JF - Brain Structure and Function
IS - 2
ER -