PUBLICATION
            GABAergic signaling linked to autophagy enhances host protection against intracellular bacterial infections
- Authors
- Kim, J.K., Kim, Y.S., Lee, H.M., Jin, H.S., Neupane, C., Kim, S., Lee, S.H., Min, J.J., Sasai, M., Jeong, J.H., Choe, S.K., Kim, J.M., Yamamoto, M., Choy, H.E., Park, J.B., Jo, E.K.
- ID
- ZDB-PUB-181012-12
- Date
- 2018
- Source
- Nature communications 9: 4184 (Journal)
- Registered Authors
- Choe, Seong-Kyu
- Keywords
- none
- MeSH Terms
- 
    
        
        
            
                - Mice, Inbred C57BL
- Receptors, GABA/metabolism
- Adenylate Kinase/metabolism
- Autophagy*/drug effects
- Mycobacterium tuberculosis/drug effects
- gamma-Aminobutyric Acid/metabolism*
- Anti-Bacterial Agents/pharmacology
- Phagosomes/drug effects
- Phagosomes/metabolism
- Phagosomes/ultrastructure
- Calcium/metabolism
- Animals
- Signal Transduction*/drug effects
- Bacterial Infections/metabolism*
- Bacterial Infections/pathology*
- Humans
- Microtubule-Associated Proteins/metabolism
- Macrophages/metabolism
- Macrophages/ultrastructure
- Host-Pathogen Interactions*/drug effects
 
- PubMed
- 30305619 Full text @ Nat. Commun.
            Citation
        
        
            Kim, J.K., Kim, Y.S., Lee, H.M., Jin, H.S., Neupane, C., Kim, S., Lee, S.H., Min, J.J., Sasai, M., Jeong, J.H., Choe, S.K., Kim, J.M., Yamamoto, M., Choy, H.E., Park, J.B., Jo, E.K. (2018) GABAergic signaling linked to autophagy enhances host protection against intracellular bacterial infections. Nature communications. 9:4184.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Gamma-aminobutyric acid (GABA) is the principal inhibitory neurotransmitter in the brain; however, the roles of GABA in antimicrobial host defenses are largely unknown. Here we demonstrate that GABAergic activation enhances antimicrobial responses against intracellular bacterial infection. Intracellular bacterial infection decreases GABA levels in vitro in macrophages and in vivo in sera. Treatment of macrophages with GABA or GABAergic drugs promotes autophagy activation, enhances phagosomal maturation and antimicrobial responses against mycobacterial infection. In macrophages, the GABAergic defense is mediated via macrophage type A GABA receptor (GABAAR), intracellular calcium release, and the GABA type A receptor-associated protein-like 1 (GABARAPL1; an Atg8 homolog). Finally, GABAergic inhibition increases bacterial loads in mice and zebrafish in vivo, suggesting that the GABAergic defense plays an essential function in metazoan host defenses. Our study identified a previously unappreciated role for GABAergic signaling in linking antibacterial autophagy to enhance host innate defense against intracellular bacterial infection.
            
    
        
        
    
    
    
                
                    
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