TY - JOUR
T1 - Fatty acids produced by the gut microbiota dampen host inflammatory responses by modulating intestinal SUMOylation
AU - Ezzine, Chaima
AU - Loison, Léa
AU - Montbrion, Nadine
AU - Bôle-Feysot, Christine
AU - Déchelotte, Pierre
AU - Coëffier, Moïse
AU - Ribet, David
N1 - Publisher Copyright:
© 2022 The Author(s). Published with license by Taylor & Francis Group, LLC.
PY - 2022/1/1
Y1 - 2022/1/1
N2 - The gut microbiota produces a wide variety of metabolites, which interact with intestinal cells and contribute to host physiology. The effect of gut commensal bacteria on host protein SUMOylation, an essential ubiquitin-like modification involved in various intestinal functions, remains, however, unknown. Here, we show that short chain fatty acids (SCFAs) and branched chain fatty acids (BCFAs) produced by the gut microbiota increase protein SUMOylation in intestinal cells in a pH-dependent manner. We demonstrate that these metabolites inactivate intestinal deSUMOylases and promote the hyperSUMOylation of nuclear matrix-associated proteins. We further show that BCFAs inhibit the NF-κB pathway, decrease pro-inflammatory cytokine expression, and promote intestinal epithelial integrity. Together, our results reveal that fatty acids produced by gut commensal bacteria regulate intestinal physiology by modulating SUMOylation and illustrate a new mechanism of dampening of host inflammatory responses triggered by the gut microbiota.
AB - The gut microbiota produces a wide variety of metabolites, which interact with intestinal cells and contribute to host physiology. The effect of gut commensal bacteria on host protein SUMOylation, an essential ubiquitin-like modification involved in various intestinal functions, remains, however, unknown. Here, we show that short chain fatty acids (SCFAs) and branched chain fatty acids (BCFAs) produced by the gut microbiota increase protein SUMOylation in intestinal cells in a pH-dependent manner. We demonstrate that these metabolites inactivate intestinal deSUMOylases and promote the hyperSUMOylation of nuclear matrix-associated proteins. We further show that BCFAs inhibit the NF-κB pathway, decrease pro-inflammatory cytokine expression, and promote intestinal epithelial integrity. Together, our results reveal that fatty acids produced by gut commensal bacteria regulate intestinal physiology by modulating SUMOylation and illustrate a new mechanism of dampening of host inflammatory responses triggered by the gut microbiota.
KW - Branched Chain Fatty Acids (BCFAs)
KW - Gut microbiota
KW - Inflammation
KW - Microbiota
KW - SUMOylation
KW - Short Chain Fatty Acids (SCFAs)
KW - Ubiquitin-like proteins
KW - host-bacteria interactions
KW - intestinal inflammation
KW - post-translational modifications
U2 - 10.1080/19490976.2022.2108280
DO - 10.1080/19490976.2022.2108280
M3 - Article
C2 - 35978476
AN - SCOPUS:85136056469
SN - 1949-0976
VL - 14
JO - Gut Microbes
JF - Gut Microbes
IS - 1
M1 - 2108280
ER -