AMPK Promotes Xenophagy through Priming of Autophagic Kinases upon Detection of Bacterial Outer Membrane Vesicles.
AMP-Activated Protein Kinase Kinases
Animals
Autophagy-Related Protein-1 Homolog
/ metabolism
Bacterial Outer Membrane
/ metabolism
Cells, Cultured
Class III Phosphatidylinositol 3-Kinases
/ metabolism
HCT116 Cells
HEK293 Cells
Host-Pathogen Interactions
Humans
MCF-7 Cells
Macroautophagy
Macrophages
/ metabolism
Mechanistic Target of Rapamycin Complex 1
/ metabolism
Mice
Mice, Inbred NOD
Protein Kinases
/ metabolism
Salmonella
/ pathogenicity
AMPK
OMV
Salmonella
ULK1
VPS34
autophagy
mTOR
outer membrane vesicles
xenophagy
Journal
Cell reports
ISSN: 2211-1247
Titre abrégé: Cell Rep
Pays: United States
ID NLM: 101573691
Informations de publication
Date de publication:
19 02 2019
19 02 2019
Historique:
received:
14
05
2018
revised:
14
12
2018
accepted:
16
01
2019
entrez:
21
2
2019
pubmed:
21
2
2019
medline:
11
4
2020
Statut:
ppublish
Résumé
The autophagy pathway is an essential facet of the innate immune response, capable of rapidly targeting intracellular bacteria. However, the initial signaling regulating autophagy induction in response to pathogens remains largely unclear. Here, we report that AMPK, an upstream activator of the autophagy pathway, is stimulated upon detection of pathogenic bacteria, before bacterial invasion. Bacterial recognition occurs through the detection of outer membrane vesicles. We found that AMPK signaling relieves mTORC1-mediated repression of the autophagy pathway in response to infection, positioning the cell for a rapid induction of autophagy. Moreover, activation of AMPK and inhibition of mTORC1 in response to bacteria is not accompanied by an induction of bulk autophagy. However, AMPK signaling is required for the selective targeting of bacteria-containing vesicles by the autophagy pathway through the activation of pro-autophagic kinase complexes. These results demonstrate a key role for AMPK signaling in coordinating the rapid autophagic response to bacteria.
Identifiants
pubmed: 30784596
pii: S2211-1247(19)30091-9
doi: 10.1016/j.celrep.2019.01.062
pii:
doi:
Substances chimiques
Protein Kinases
EC 2.7.-
Class III Phosphatidylinositol 3-Kinases
EC 2.7.1.137
Autophagy-Related Protein-1 Homolog
EC 2.7.11.1
Mechanistic Target of Rapamycin Complex 1
EC 2.7.11.1
AMP-Activated Protein Kinase Kinases
EC 2.7.11.3
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
2150-2165.e5Subventions
Organisme : CIHR
ID : PJT153034
Pays : Canada
Organisme : CIHR
ID : PJT148634
Pays : Canada
Organisme : CIHR
ID : MSH141981
Pays : Canada
Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.