Both partial inactivation as well as activation of NF-κB signaling lead to hypertension and chronic kidney disease
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články
Grantová podpora
32170825
NSFC
2023A1515010424
Guangdong Natural Science Foundation
202201020007
Science and Technology Planning Project of Guangzhou
Boehringer Ingelheim
21621106
Research Funds for the Central Universities
Research Grant of Key Laboratory of Regenerative Medicine
Ministry of Education
ZSYXM202217
Jinan University
A2020503
Guangdong Medical Research Foundation
202310559057
National Innovation and Entrepreneurship Training Program for Undergraduate
PubMed
38614958
DOI
10.1093/ndt/gfae090
PII: 7645469
Knihovny.cz E-zdroje
- Klíčová slova
- NF-κB mutant mice, NF-κB signalling, chronic kidney disease, hypertension, inflammation,
- MeSH
- chronická renální insuficience metabolismus patologie etiologie MeSH
- fibróza MeSH
- hypertenze * metabolismus etiologie MeSH
- kvantitativní polymerázová řetězová reakce MeSH
- modely nemocí na zvířatech MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- NF-kappa B * metabolismus MeSH
- signální transdukce * MeSH
- western blotting MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- NF-kappa B * MeSH
BACKGROUND: Activation of nuclear factor-kappa B (NF-κB) signalling is key in the pathogenesis of chronic kidney disease (CKD). However, a certain level of NF-κB activity is necessary to enable tissue repair. METHODS: The relationship between activated and inactivated NF-κB signaling and the pathogenesis of CKD was investigated using mouse models of NF-κB partial inactivation (mutating cysteine at position 59 of the sixth exon on the NF-κB gene into alanine) and activation (mutating cysteine at position 59 of the sixth exon on the NF-κB gene into serine). RESULTS: The density of CD3, CD8, CD68 positive cells, as well as the expression of interleukin 6, Tumor necrosis factor receptor associated factor 1 and Nef-associated factor 1 in the kidney tissues of NF-κBC59A mice were reduced, whereas an opposing pattern was observed in the NF-κBC59S mice. Blood pressure, kidney fibrosis (analyzed by periodic acid-Schiff, Masson trichrome and Sirius Red staining, as well as α-SMA immunofluorescence), serum creatinine and urinary albumin-to-creatinine ratio are markedly increased in NF-κB-activated and -inactivated mice compared with controls. Transmission electron microscopy indicated that the glomerular basement membrane was thicker in both NF-κBC59A and NF-κBC59S mice compared with wild-type mice. CONCLUSIONS: Using mice models with partially activated and inactivated NF-κB pathways suggests that there is an apparently U-shaped relationship between blood pressure, kidney function as well as morphology and the activation of the NF-κB pathway. A certain optimal activity of the NF-κB pathway seems to be important to maintain optimal kidney function and morphology.
2nd Medical Faculty Charles University Prague Prague Czech Republic
Clinical Research Center Clifford Hospital Guangzhou China
Department of Pathology 1st Affiliated Hospital of Jinan University Guangzhou China
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