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Sympathetic nervous system controls resolution of inflammation via regulation of repulsive guidance molecule A.


ABSTRACT: The bidirectional communication between the immune and nervous system is important in regulating immune responses. Here we show that the adrenergic nerves of sympathetic nervous system orchestrate inflammation resolution and regenerative programs by modulating repulsive guidance molecule A (RGM-A). In murine peritonitis, adrenergic nerves and RGM-A show bidirectional activation by stimulating the mutual expression and exhibit a higher potency for the cessation of neutrophil infiltration; this reduction is accompanied by increased pro-resolving monocyte or macrophage recruitment, polymorphonucleocyte clearance and specialized pro-resolving lipid mediators production at sites of injury. Chemical sympathectomy results in hyperinflammation and ineffective resolution in mice, while RGM-A treatments reverse these phenotypes. Signalling network analyses imply that RGM-A and ?2AR agonist regulate monocyte activation by suppressing NF-?B activity but activating RICTOR and PI3K/AKT signalling. Our results thus illustrate the function of sympathetic nervous system and RGM-A in regulating resolution and tissue repair in a murine acute peritonitis model.

SUBMITTER: Korner A 

PROVIDER: S-EPMC6367413 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

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Sympathetic nervous system controls resolution of inflammation via regulation of repulsive guidance molecule A.

Körner Andreas A   Schlegel Martin M   Kaussen Torsten T   Gudernatsch Verena V   Hansmann Georg G   Schumacher Timo T   Giera Martin M   Mirakaj Valbona V  

Nature communications 20190207 1


The bidirectional communication between the immune and nervous system is important in regulating immune responses. Here we show that the adrenergic nerves of sympathetic nervous system orchestrate inflammation resolution and regenerative programs by modulating repulsive guidance molecule A (RGM-A). In murine peritonitis, adrenergic nerves and RGM-A show bidirectional activation by stimulating the mutual expression and exhibit a higher potency for the cessation of neutrophil infiltration; this re  ...[more]

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