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Nod-like receptors are critical for gut-brain axis signaling

Authors :
Kyle Akio Wong
Mélanie G. Gareau
Mariana X. Byndloss
Cristina Torres-Fuentes
Mariana Barboza
Patricia Stokes
Bäumler Aj
Gonzalo Rabasa
Jessica A. Sladek
Ingrid Brust-Mascher
Richard L. Ferrero
Charles Maisonneuve
Gillis Se
Dana J. Philpott
Matteo M. Pusceddu
Melinda Schneider
Goldfild Lr
Carlito B. Lebrilla
Kim E. Barrett
Colin Reardon
Publication Year :
2019
Publisher :
Cold Spring Harbor Laboratory, 2019.

Abstract

Gut-brain axis signaling is critical for maintaining health and homeostasis. Stressful life events can impact gut-brain signaling, leading to altered mood, cognition and intestinal dysfunction. Here we identify nucleotide binding oligomerization domain (Nod)-like receptors (NLR), Nod1 and Nod2, as novel regulators for gut-brain signaling. NLR are innate immune pattern recognition receptors expressed in the gut and brain, important in the regulation of gastrointestinal (GI) physiology. We found that mice deficient in both Nod1 and Nod2 (NodDKO) demonstrate signs of stress-induced anxiety, cognitive impairment and depression in the context of a hyperactive hypothalamic-pituitary-adrenal axis. These deficits were coupled with impairments in the serotonergic pathway in the brain, decreased hippocampal neurogenesis, and reduced neural activation. In addition, NodDKO mice had increased GI permeability and altered serotonin signaling in the gut following exposure to acute stress. Administration of the selective serotonin reuptake inhibitor, fluoxetine, abrogated behavioral impairments and restored serotonin signaling. We also identified that intestinal epithelial cell-specific deletion of Nod1 (VilCre+Nod1f/f), but not Nod2, increased susceptibility to stress-induced anxiety-like behavior and cognitive impairment following exposure to stress. Together these data suggest that intestinal epithelial NLR are novel modulators of gut-brain communication and may serve as potential novel therapeutic targets for the treatment of gut-brain disorders.

Details

Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....2274e2a8f8413928360a2206ea9282b4