Transcriptomic and Network Analyses Reveal Immune Modulation by Endocannabinoids in Approach/Avoidance Traits
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...
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creator | Termine, Andrea Fabrizio, Carlo Gimenez, Juliette Panuccio, Anna Balsamo, Francesca Passarello, Noemi Caioli, Silvia Saba, Luana De Bardi, Marco Della Valle, Francesco Orlando, Valerio Petrosini, Laura Laricchiuta, Daniela |
description | 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. |
doi_str_mv | 10.3390/ijms23052538 |
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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.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms23052538</identifier><identifier>PMID: 35269678</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Adaptive immunity ; Amygdala ; Amygdala - metabolism ; Animals ; Avoidance ; Behavior ; Cannabinoid CB1 receptors ; Chemokines ; Cytokines ; Endocannabinoid system ; Endocannabinoids - metabolism ; Gene expression ; Homeostasis ; Immune response ; Immune system ; Immunomodulation ; Inflammation ; Metabolism ; Mice ; Neural networks ; Neuronal Plasticity ; Neurons ; Neurons - metabolism ; Proteins ; Psychopathology ; Pyramidal cells ; Receptor, Cannabinoid, CB1 - genetics ; Receptor, Cannabinoid, CB1 - metabolism ; Synaptic plasticity ; Transcriptome ; Transcriptomics</subject><ispartof>International journal of molecular sciences, 2022-02, Vol.23 (5), p.2538</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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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.</description><subject>Adaptive immunity</subject><subject>Amygdala</subject><subject>Amygdala - metabolism</subject><subject>Animals</subject><subject>Avoidance</subject><subject>Behavior</subject><subject>Cannabinoid CB1 receptors</subject><subject>Chemokines</subject><subject>Cytokines</subject><subject>Endocannabinoid system</subject><subject>Endocannabinoids - metabolism</subject><subject>Gene expression</subject><subject>Homeostasis</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Immunomodulation</subject><subject>Inflammation</subject><subject>Metabolism</subject><subject>Mice</subject><subject>Neural networks</subject><subject>Neuronal Plasticity</subject><subject>Neurons</subject><subject>Neurons - metabolism</subject><subject>Proteins</subject><subject>Psychopathology</subject><subject>Pyramidal cells</subject><subject>Receptor, Cannabinoid, CB1 - 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metabolism</topic><topic>Animals</topic><topic>Avoidance</topic><topic>Behavior</topic><topic>Cannabinoid CB1 receptors</topic><topic>Chemokines</topic><topic>Cytokines</topic><topic>Endocannabinoid system</topic><topic>Endocannabinoids - metabolism</topic><topic>Gene expression</topic><topic>Homeostasis</topic><topic>Immune response</topic><topic>Immune system</topic><topic>Immunomodulation</topic><topic>Inflammation</topic><topic>Metabolism</topic><topic>Mice</topic><topic>Neural networks</topic><topic>Neuronal Plasticity</topic><topic>Neurons</topic><topic>Neurons - metabolism</topic><topic>Proteins</topic><topic>Psychopathology</topic><topic>Pyramidal cells</topic><topic>Receptor, Cannabinoid, CB1 - genetics</topic><topic>Receptor, Cannabinoid, CB1 - metabolism</topic><topic>Synaptic plasticity</topic><topic>Transcriptome</topic><topic>Transcriptomics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Termine, Andrea</creatorcontrib><creatorcontrib>Fabrizio, Carlo</creatorcontrib><creatorcontrib>Gimenez, Juliette</creatorcontrib><creatorcontrib>Panuccio, Anna</creatorcontrib><creatorcontrib>Balsamo, Francesca</creatorcontrib><creatorcontrib>Passarello, Noemi</creatorcontrib><creatorcontrib>Caioli, Silvia</creatorcontrib><creatorcontrib>Saba, Luana</creatorcontrib><creatorcontrib>De Bardi, Marco</creatorcontrib><creatorcontrib>Della Valle, Francesco</creatorcontrib><creatorcontrib>Orlando, Valerio</creatorcontrib><creatorcontrib>Petrosini, Laura</creatorcontrib><creatorcontrib>Laricchiuta, Daniela</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - 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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. 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subjects | Adaptive immunity Amygdala Amygdala - metabolism Animals Avoidance Behavior Cannabinoid CB1 receptors Chemokines Cytokines Endocannabinoid system Endocannabinoids - metabolism Gene expression Homeostasis Immune response Immune system Immunomodulation Inflammation Metabolism Mice Neural networks Neuronal Plasticity Neurons Neurons - metabolism Proteins Psychopathology Pyramidal cells Receptor, Cannabinoid, CB1 - genetics Receptor, Cannabinoid, CB1 - metabolism Synaptic plasticity Transcriptome Transcriptomics |
title | Transcriptomic and Network Analyses Reveal Immune Modulation by Endocannabinoids in Approach/Avoidance Traits |
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