Search: onr:"swepub:oai:DiVA.org:oru-66388" >
Activation of the N...
Activation of the NLRP3 Inflammasome Pathway by Uropathogenic Escherichia coli Is Virulence Factor-Dependent and Influences Colonization of Bladder Epithelial Cells
-
- Demirel, Isak, 1987- (author)
- Örebro universitet,Institutionen för medicinska vetenskaper,iRiSC - Inflammatory Response and Infection Susceptibility Centre
-
- Persson, Alexander, 1978- (author)
- Örebro universitet,Institutionen för medicinska vetenskaper,iRiSC - Inflammatory Response and Infection Susceptibility Centre
-
- Brauner, Annelie (author)
- Karolinska Institutet
-
show more...
-
- Särndahl, Eva, 1963- (author)
- Örebro universitet,Institutionen för medicinska vetenskaper,iRiSC - Inflammatory Response and Infection Susceptibility Centre
-
- Kruse, Robert, 1972- (author)
- Örebro universitet,Institutionen för medicinska vetenskaper,Department of Clinical Research Laboratory, Faculty of Health and Medical Sciences, Örebro University, Örebro, Sweden,iRiSC - Inflammatory Response and Infection Susceptibility Centre
-
- Persson, Katarina, 1962- (author)
- Örebro universitet,Institutionen för medicinska vetenskaper,iRiSC - Inflammatory Response and Infection Susceptibility Centre
-
show less...
-
(creator_code:org_t)
- 2018-03-14
- 2018
- English.
-
In: Frontiers in Cellular and Infection Microbiology. - : Frontiers Media S.A.. - 2235-2988. ; 8
- Related links:
-
https://doi.org/10.3...
-
show more...
-
https://www.frontier...
-
https://urn.kb.se/re...
-
https://doi.org/10.3...
-
http://kipublication...
-
show less...
Abstract
Subject headings
Close
- The NLRP3 inflammasome and IL-1 beta release have recently been suggested to be important for the progression of urinary tract infection (UTI). However, much is still unknown regarding the interaction of UPEC and the NLRP3 inflammasome. The purpose of this study was to elucidate what virulence factors uropathogenic Escherichia coil (UPEC) use to modulate NLRP3 inflammasome activation and subsequent IL-1 beta release and the role of NLRP3 for UPEC colonization of bladder epithelial cells. The bladder epithelial cell line 5637, CRISPR/Cas9 generated NLRP3, caspase-1 and mesotrypsin deficient cell lines and transformed primary bladder epithelial cells (HBLAK) were stimulated with UPEC isolates and the non-pathogenic MG1655 strain. We found that the UPEC strain CFT073, but not MG1655, induced an increased caspase-1 activity and IL-1 beta release from bladder epithelial cells. The increase was shown to be mediated by et-hemolysin activation of the NLRP3 inflammasome in an NE-kappa B-independent manner. The effect of-hemolysin on IL-1 beta release was biphasic, initially suppressive, later inductive. Furthermore, the phase-locked type-1-fimbrial ON variant of CFT073 inhibited caspase-1 activation and IL-1 beta release. In addition, the ability of CFT073 to adhere to and invade NLRP3 deficient cells was significantly reduced compare to wild-type cells. The reduced colonization of NLRP3-deficient cells was type-1 fimbriae dependent. In conclusion, we found that the NLRP3 inflammasome was important for type-1 fimbriae-dependent colonization of bladder epithelial cells and that both type-1 fimbriae and alpha-hemolysin can modulate the activity of the NLRP3 inflammasome.
Subject headings
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Immunology in the medical area (hsv//eng)
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Mikrobiologi inom det medicinska området (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Microbiology in the medical area (hsv//eng)
Keyword
- UPEC
- NLRP3 inflammasome
- IL-1 beta
- alpha-hemolysin
- type-1 fimbriae
Publication and Content Type
- ref (subject category)
- art (subject category)
Find in a library
To the university's database