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Neutrophil Extracellular Traps Initiate Gallstone Formation
- Source :
- Immunity. 51:443-450.e4
- Publication Year :
- 2019
- Publisher :
- Elsevier BV, 2019.
-
Abstract
- The presence of gallstones (cholelithiasis) is a highly prevalent and severe disease and one of the leading causes of hospital admissions worldwide. Due to its substantial health impact, we investigated the biological mechanisms that lead to the formation and growth of gallstones. We show that gallstone assembly essentially requires neutrophil extracellular traps (NETs). We found consistent evidence for the presence of NETs in human and murine gallstones and describe an immune-mediated process requiring activation of the innate immune system for the formation and growth of gallstones. Targeting NET formation via inhibition of peptidyl arginine deiminase type 4 or abrogation of reactive oxygen species (ROS) production, as well as damping of neutrophils by metoprolol, effectively inhibit gallstone formation in vivo. Our results show that after the physicochemical process of crystal formation, NETs foster their assembly into larger aggregates and finally gallstones. These insights provide a feasible therapeutic concept to prevent cholelithiasis in patients at risk.
- Subjects :
- Male
0301 basic medicine
Neutrophils
Immunology
Gallstones
Biology
Extracellular Traps
Mice
03 medical and health sciences
0302 clinical medicine
In vivo
medicine
Animals
Humans
Immunology and Allergy
Peptidyl arginine deiminase
In patient
ddc:616
chemistry.chemical_classification
Mice, Inbred BALB C
Reactive oxygen species
Innate immune system
Neutrophil extracellular traps
medicine.disease
Immunity, Innate
3. Good health
Mice, Inbred C57BL
030104 developmental biology
Infectious Diseases
chemistry
030220 oncology & carcinogenesis
PADI4
Cancer research
Female
Reactive Oxygen Species
Subjects
Details
- ISSN :
- 10747613
- Volume :
- 51
- Database :
- OpenAIRE
- Journal :
- Immunity
- Accession number :
- edsair.doi.dedup.....64d54205ec67867b812031ab81ddb1f9
- Full Text :
- https://doi.org/10.1016/j.immuni.2019.07.002