Lysosome Fusion Maintains Phagosome Integrity during Fungal Infection.
Animals
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
/ metabolism
Calcium
/ metabolism
Candida albicans
/ growth & development
Cell Death
Cell Line
Cells, Cultured
Gene Expression Profiling
Host Microbial Interactions
Hyphae
/ growth & development
Inflammasomes
/ metabolism
Interleukin-1beta
/ metabolism
Lysosomes
/ physiology
Macrophages
/ microbiology
Male
Membrane Fusion
Mice
Mice, Inbred C57BL
Mice, Knockout
Mycoses
/ metabolism
NLR Family, Pyrin Domain-Containing 3 Protein
/ metabolism
Phagocytosis
Phagosomes
/ physiology
Candida albicans
NLRP3
calcium
fungi
hypha
inflammasome
lysosome
macrophage
phagocytosis
phagosome
Journal
Cell host & microbe
ISSN: 1934-6069
Titre abrégé: Cell Host Microbe
Pays: United States
ID NLM: 101302316
Informations de publication
Date de publication:
09 12 2020
09 12 2020
Historique:
received:
24
09
2019
revised:
10
08
2020
accepted:
02
09
2020
pubmed:
7
10
2020
medline:
20
7
2021
entrez:
6
10
2020
Statut:
ppublish
Résumé
Phagosomes must maintain membrane integrity to exert their microbicidal function. Some microorganisms, however, survive and grow within phagosomes. In such instances, phagosomes must expand to avoid rupture and microbial escape. We studied whether phagosomes regulate their size to preserve integrity during infection with the fungal pathogen Candida albicans. Phagosomes release calcium as C. albicans hyphae elongate, inducing lysosome recruitment and insertion, thereby increasing the phagosomal surface area. As hyphae grow, the expanding phagosome consumes the majority of free lysosomes. Simultaneously, lysosome biosynthesis is stimulated by activation of TFEB, a transcriptional regulator of lysosomal biogenesis. Preventing lysosomal insertion causes phagosomal rupture, NLRP3 inflammasome activation, IL-1β secretion and host-cell death. Whole-genome transcriptomic analysis demonstrate that stress responses elicited in C. albicans upon engulfment are reversed if phagosome expansion is prevented. Our findings reveal a mechanism whereby phagosomes maintain integrity while expanding, ensuring that growing pathogens remain entrapped within this microbicidal compartment.
Identifiants
pubmed: 33022213
pii: S1931-3128(20)30505-9
doi: 10.1016/j.chom.2020.09.004
pii:
doi:
Substances chimiques
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
0
IL1B protein, mouse
0
Inflammasomes
0
Interleukin-1beta
0
NLR Family, Pyrin Domain-Containing 3 Protein
0
Nlrp3 protein, mouse
0
Tcfeb protein, mouse
0
Calcium
SY7Q814VUP
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
798-812.e6Commentaires et corrections
Type : CommentIn
Type : CommentIn
Informations de copyright
Copyright © 2020 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Interests The authors declare no competing interests.