Deletion of Maged1 in mice abolishes locomotor and reinforcing effects of cocaine

• Published in: EMBO reports Vol. 19; no. 9
• Main Authors: De Backer, Jean‐François, Monlezun, Stéphanie, Detraux, Bérangère, Gazan, Adeline, Vanopdenbosch, Laura, Cheron, Julian, Cannazza, Giuseppe, Valverde, Sébastien, Cantacorps, Lídia, Nassar, Mérie, Venance, Laurent, Valverde, Olga, Faure, Philippe, Zoli, Michele, De Backer, Olivier, Gall, David, Schiffmann, Serge N, de Kerchove d'Exaerde, Alban
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01-09-2018; Blackwell Publishing Ltd; Wiley-Blackwell; EMBO Press; John Wiley and Sons Inc
• Subjects: Addictions; Amygdala; Amygdala - drug effects; Amygdala - physiology; Animal behavior; Animals; Behavior, Addictive - genetics; Brain; Brain slice preparation; Clonal deletion; Cocaine; Cocaine - administration & dosage; Cocaine - pharmacology; Cocaine-Related Disorders - genetics; Conditioning; Dependovirus; Dopamine; Dopamine - metabolism; Dopamine receptors; Drug abuse; Drug addiction; Drug sensitization; EMBO27; Gene Deletion; Genes; Glutamic Acid - metabolism; Life Sciences; Locomotion - drug effects; Locomotion - genetics; Male; Melanoma; Mice; Mice, Knockout; Narcotics; Neoplasm Proteins - genetics; Neoplasm Proteins - physiology; Neostriatum; Neurons - metabolism; Neurotransmission; Nucleus accumbens; Nucleus Accumbens - drug effects; Nucleus Accumbens - metabolism; Overflow; Place preference conditioning; Prefrontal cortex; Prefrontal Cortex - drug effects; Prefrontal Cortex - physiology; Reinforcement (Psychology); Rodents; Synaptic Transmission - genetics; Synaptic Transmission - physiology; Tumors; γ-Aminobutyric acid; amygdala; nucleus accumbens; dopamine; prefrontal cortex; drug sensitization; amygdala, Amygdala, Animals, Behavior, Addictive, Cocaine, Cocaine-Related Disorders, Dependovirus, dopamine, Dopamine, drug sensitization, Gene Deletion, Glutamic Acid, Locomotion, Male, Mice, Mice, Knockout, Neoplasm Proteins, Neurons, nucleus accumbens, Nucleus Accumbens, prefrontal cortex, Prefrontal Cortex, Reinforcement, Psychology, Synaptic Transmission
• ISSN: 1469-221X; 1469-3178
• DOI: 10.15252/embr.201745089

Melanoma antigen genes (Mage) were first described as tumour markers. However, some of Mage are also expressed in healthy cells where their functions remain poorly understood. Here, we describe an unexpected role for one of these genes, Maged1, in the control of behaviours related to drug addiction. Mice lacking Maged1 are insensitive to the behavioural effects of cocaine as assessed by locomotor sensitization, conditioned place preference (CPP) and drug self‐administration. Electrophysiological experiments in brain slices and conditional knockout mice demonstrate that Maged1 is critical for cortico‐accumbal neurotransmission. Further, expression of Maged1 in the prefrontal cortex (PFC) and the amygdala, but not in dopaminergic or striatal and other GABAergic neurons, is necessary for cocaine‐mediated behavioural sensitization, and its expression in the PFC is also required for cocaine‐induced extracellular dopamine (DA) release in the nucleus accumbens (NAc). This work identifies Maged1 as a critical molecule involved in cellular processes and behaviours related to addiction.
Synopsis
Identification of genes underlying physiological changes induced by drugs of abuse provides molecular insight into addiction. This study reveals that Maged1 is required for the expression of behavioural effects of cocaine in mice.
Mice lacking Maged1 are insensitive to the locomotor, rewarding and reinforcing effects of cocaine.
Cocaine‐induced dopamine overflow in the striatum is impaired in mice lacking Maged1.
Conditional Maged1 deletion in the prefrontal cortex selectively impairs locomotor sensitization to cocaine and cocaine‐induced dopamine overflow.
Graphical Abstract
Identification of genes underlying physiological changes induced by drugs of abuse provides molecular insight into addiction. This study reveals that Maged1 is required for the expression of behavioural effects of cocaine in mice.