Interleukin-36 cytokines alter the intestinal microbiome and can protect against obesity and metabolic dysfunction.
Akkermansia
Animals
Colon
/ immunology
Cytokines
/ metabolism
Diabetes Mellitus, Type 2
Gastrointestinal Microbiome
/ immunology
Gene Expression
Glucose Tolerance Test
Host Microbial Interactions
/ immunology
Humans
Inflammation Mediators
/ metabolism
Insulin Resistance
Interleukin-1
/ genetics
Male
Metabolic Diseases
/ metabolism
Mice
Mice, Inbred C57BL
Mice, Knockout
Mucin-2
/ metabolism
Obesity
/ immunology
Receptors, Interleukin-1
/ genetics
Transcriptome
Verrucomicrobia
Journal
Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555
Informations de publication
Date de publication:
05 09 2019
05 09 2019
Historique:
received:
03
05
2018
accepted:
13
08
2019
entrez:
7
9
2019
pubmed:
7
9
2019
medline:
7
1
2020
Statut:
epublish
Résumé
Members of the interleukin-1 (IL-1) family are important mediators of obesity and metabolic disease and have been described to often play opposing roles. Here we report that the interleukin-36 (IL-36) subfamily can play a protective role against the development of disease. Elevated IL-36 cytokine expression is found in the serum of obese patients and negatively correlates with blood glucose levels among those presenting with type 2 diabetes. Mice lacking IL-36Ra, an IL-36 family signalling antagonist, develop less diet-induced weight gain, hyperglycemia and insulin resistance. These protective effects correlate with increased abundance of the metabolically protective bacteria Akkermansia muciniphila in the intestinal microbiome. IL-36 cytokines promote its outgrowth as well as increased colonic mucus secretion. These findings identify a protective role for IL-36 cytokines in obesity and metabolic disease, adding to the current understanding of the role the broader IL-1 family plays in regulating disease pathogenesis.
Identifiants
pubmed: 31488830
doi: 10.1038/s41467-019-11944-w
pii: 10.1038/s41467-019-11944-w
pmc: PMC6728358
doi:
Substances chimiques
Cytokines
0
Inflammation Mediators
0
Interleukin-1
0
Muc2 protein, mouse
0
Mucin-2
0
Receptors, Interleukin-1
0
interleukin 36, human
0
interleukin-36 receptor, mouse
0
interleukin-36, mouse
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
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