Outer membrane vesicles of Porphyromonas gingivalis attenuate insulin sensitivity by delivering gingipains to the liver.
Animals
Bacterial Outer Membrane
/ metabolism
Disease Models, Animal
Gingipain Cysteine Endopeptidases
/ genetics
Glycogen Synthase Kinase 3 beta
/ genetics
Humans
Insulin Resistance
/ genetics
Liver
/ metabolism
Mice
Periodontitis
/ genetics
Porphyromonas gingivalis
/ genetics
Proto-Oncogene Proteins c-akt
/ genetics
Signal Transduction
/ genetics
Diabetes mellitus
Insulin resistance
Outer membrane vesicles
Periodontal disease
Porphyromonas gingivalis
Journal
Biochimica et biophysica acta. Molecular basis of disease
ISSN: 1879-260X
Titre abrégé: Biochim Biophys Acta Mol Basis Dis
Pays: Netherlands
ID NLM: 101731730
Informations de publication
Date de publication:
01 06 2020
01 06 2020
Historique:
received:
12
09
2019
revised:
12
02
2020
accepted:
13
02
2020
pubmed:
24
2
2020
medline:
21
10
2020
entrez:
24
2
2020
Statut:
ppublish
Résumé
Outer membrane vesicles (OMVs) are nanosized particles derived from the outer membrane of gram-negative bacteria. Oral bacterium Porphyromonas gingivalis (Pg) is known to be a major pathogen of periodontitis that contributes to the progression of periodontal disease by releasing OMVs. The effect of Pg OMVs on systemic diseases is still unknown. To verify whether Pg OMVs affect the progress of diabetes mellitus, we analyzed the cargo proteins of vesicles and evaluated their effect on hepatic glucose metabolism. Here, we show that Pg OMVs were equipped with Pg-derived proteases gingipains and translocated to the liver in mice. In these mice, the hepatic glycogen synthesis in response to insulin was decreased, and thus high blood glucose levels were maintained. Pg OMVs also attenuated the insulin-induced Akt/glycogen synthase kinase-3 β (GSK-3β) signaling in a gingipain-dependent fashion in hepatic HepG2 cells. These results suggest that the delivery of gingipains mediated by Pg OMV elicits changes in glucose metabolisms in the liver and contributes to the progression of diabetes mellitus.
Identifiants
pubmed: 32088316
pii: S0925-4439(20)30076-4
doi: 10.1016/j.bbadis.2020.165731
pii:
doi:
Substances chimiques
Gingipain Cysteine Endopeptidases
0
Glycogen Synthase Kinase 3 beta
EC 2.7.11.1
Proto-Oncogene Proteins c-akt
EC 2.7.11.1
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
165731Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.