Abstract

Approach and avoidance (A/A) tendencies are stable behavioral traits in responding to rewarding and fearful stimuli. They represent the superordinate division of emotion, and individual differences in such traits are associated with disease susceptibility. The neural circuitry underlying A/A traits is retained to be the cortico-limbic pathway including the amygdala, the central hub for the emotional processing. Furthermore, A/A-specific individual differences are associated with the activity of the endocannabinoid system (ECS) and especially of CB1 receptors whose density and functionality in amygdala differ according to A/A traits. ECS markedly interacts with the immune system (IS). However, how the interplay between ECS and IS is associated with A/A individual differences is still ill-defined. To fill this gap, here we analyzed the interaction between the gene expression of ECS and immune system (IS) in relation to individual differences. To unveil the deep architecture of ECS-IS interaction, we performed cell-specific transcriptomics analysis. Differential gene expression profiling, functional enrichment, and protein–protein interaction network analyses were performed in amygdala pyramidal neurons of mice showing different A/A behavioral tendencies. Several altered pro-inflammatory pathways were identified as associated with individual differences in A/A traits, indicating the chronic activation of the adaptive immune response sustained by the interplay between endocannabinoids and the IS. Furthermore, results showed that the interaction between the two systems modulates synaptic plasticity and neuronal metabolism in individual difference-specific manner. Deepening our knowledge about ECS/IS interaction may provide useful targets for treatment and prevention of psychopathology associated with A/A traits.

Highlights

  • Responding to rewarding and fearful stimuli is characterized by individual differences ranging from approach to avoidance (A/A) tendencies, behavioral traits relatively stable over time and across conditions that require balancing potential risks against rewards in uncertain environments [1,2]

  • In the comparison between BA and AV mice, several Differentially expressed genes (DEGs) belonging to the proinflammatory cytokines including tumor necrosis factor α (TNFα), interleukin-2 (IL-2), and interleukin-12 (IL-12), were identified (Supplementary Table Session 1 (S1))

  • The expression of genes involved in the production and regulation of cytokines significantly differed between BA and AV mice, since DEGs significantly enriched IL-2 and IL-12 production pathways (GO:0032623; p.adjusted = 0.03; Gene Ontology (GO):0032615; p.adjusted = 0.03), as well as the

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Summary

Introduction

Responding to rewarding and fearful stimuli is characterized by individual differences ranging from approach to avoidance (A/A) tendencies, behavioral traits relatively stable over time and across conditions that require balancing potential risks against rewards in uncertain environments [1,2]. The ECS is a neuromodulatory system, which acts as a retrograde feedback mechanism at both excitatory and inhibitory synapses, primarily responsible for maintaining homeostasis, balance in internal environment (temperature, mood, and immune system), and energy input and output in biological systems [18,19]. It comprises classical (Cannabinoid receptor type 1 and 2; CB1, CB2) and non-classical (transient receptor potential cation channel subfamily V member 1 and 2; TRPV1 and TRPV2) receptors, their endogenous ligands (endocannabinoids (EC): anandamide (AEA), 2-arachidonoylglycerol (2-AG), 2-arachidonyl glyceryl ether (2-AGE), N-arachidonoyl dopamine (NADA), palmitoylethanolamide (PEA)), and enzymes involved in endocannabinoid metabolism (fatty acid amide hydrolase (FAAH), N-acyl phosphatidylethanolamine phospholipase D (NAPEPLD), palmitoylethanolamidepreferring acid amidase (PAA)) [20]. While CB2 receptors are primarily expressed in the cells of the immune system, CB1 receptors are densely present in the brain areas responsible for learning and memory, movement, hormone regulation, body temperature, sensory perception, reward, emotions, and individual differences traits [21]

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