The Prostaglandin E2-EP3 Receptor Axis Regulates Anaplasma phagocytophilum-Mediated NLRC4 Inflammasome Activation
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural
Grantová podpora
R01 AI119073
NIAID NIH HHS - United States
T32 AI007517
NIAID NIH HHS - United States
R01 AI093653
NIAID NIH HHS - United States
R01 DK072381
NIDDK NIH HHS - United States
R01 AI097518
NIAID NIH HHS - United States
R01 AI101055
NIAID NIH HHS - United States
PubMed
27482714
PubMed Central
PMC4970705
DOI
10.1371/journal.ppat.1005803
PII: PPATHOGENS-D-16-00215
Knihovny.cz E-zdroje
- MeSH
- Anaplasma phagocytophilum imunologie MeSH
- dinoproston imunologie MeSH
- ehrlichióza imunologie MeSH
- ELISA MeSH
- imunoblotting MeSH
- inflamasomy imunologie MeSH
- kvantitativní polymerázová řetězová reakce MeSH
- modely nemocí na zvířatech MeSH
- myši inbrední C57BL MeSH
- myši knockoutované MeSH
- myši MeSH
- proteiny regulující apoptózu imunologie MeSH
- proteiny vázající vápník imunologie MeSH
- receptory prostaglandinů E - podtyp EP3 imunologie MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- dinoproston MeSH
- inflamasomy MeSH
- Ipaf protein, mouse MeSH Prohlížeč
- proteiny regulující apoptózu MeSH
- proteiny vázající vápník MeSH
- receptory prostaglandinů E - podtyp EP3 MeSH
Rickettsial agents are sensed by pattern recognition receptors but lack pathogen-associated molecular patterns commonly observed in facultative intracellular bacteria. Due to these molecular features, the order Rickettsiales can be used to uncover broader principles of bacterial immunity. Here, we used the bacterium Anaplasma phagocytophilum, the agent of human granulocytic anaplasmosis, to reveal a novel microbial surveillance system. Mechanistically, we discovered that upon A. phagocytophilum infection, cytosolic phospholipase A2 cleaves arachidonic acid from phospholipids, which is converted to the eicosanoid prostaglandin E2 (PGE2) via cyclooxygenase 2 (COX2) and the membrane associated prostaglandin E synthase-1 (mPGES-1). PGE2-EP3 receptor signaling leads to activation of the NLRC4 inflammasome and secretion of interleukin (IL)-1β and IL-18. Importantly, the receptor-interacting serine/threonine-protein kinase 2 (RIPK2) was identified as a major regulator of the immune response against A. phagocytophilum. Accordingly, mice lacking COX2 were more susceptible to A. phagocytophilum, had a defect in IL-18 secretion and exhibited splenomegaly and damage to the splenic architecture. Remarkably, Salmonella-induced NLRC4 inflammasome activation was not affected by either chemical inhibition or genetic ablation of genes associated with PGE2 biosynthesis and signaling. This divergence in immune circuitry was due to reduced levels of the PGE2-EP3 receptor during Salmonella infection when compared to A. phagocytophilum. Collectively, we reveal the existence of a functionally distinct NLRC4 inflammasome illustrated by the rickettsial agent A. phagocytophilum.
Department of Pathology University of Texas Medical Branch Galveston Texas United States of America
Institute of Parasitology Biology Centre Czech Academy of Sciences Budweis Czech Republic
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