HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

TNFα Induces Multidrug Resistance-Associated Protein 4 Expression through p38-E2F1-Nrf2 Signaling in Obstructive Cholestasis.

AbstractPURPOSE:
To explore the molecular mechanism of the upregulation of multidrug resistance-associated protein 4 (MRP4) in cholestasis.
MATERIALS AND METHODS:
The mRNA and protein levels of MRP4 in liver samples from cholestatic patients were determined by quantitative real-time PCR and Western blot. In human hepatoma HepG2 cells, electrophoretic mobility shift assay (EMSA) was used to determine the affinity of nuclear factor-E2-related factor (Nrf2) binding to MRP4 promoter. Dual-luciferase reporter assay was used to detect the binding of tumor necrosis factor α (TNFα) to the promotor of E2F1. The bile duct ligation mouse models were established using male C57BL/6 mice.
RESULTS:
The mRNA and protein levels of MRP4 were significantly increased in cholestatic patients. TNFα treatment induced the expression of MRP4 and Nrf2 and enhanced cell nuclear extract binding activity to MRP4 promoter, as demonstrated by EMSA. Nrf2 knockdown reduced MRP4 mRNA levels in both HepG2 and Hep-3B cells. In addition, TNFα increased Rb phosphorylation and expression of MRP4 and Nrf2 and activated E2F1 and phosphorylated p38 in HepG2 and Hep-3B cells. These effects were markedly inhibited by pretreatment with E2F1 siRNA. Dual-luciferase reporter assay validated that TNFα induces the transcription of E2F1. Furthermore, the expression of MRP4, Nrf2, E2F1, and p-p38 proteins was improved with treatment of TNFα in a mouse model of cholestasis. E2F1 siRNA lentivirus or SB 203580 (p38 inhibitor) inhibited these positive effects.
CONCLUSION:
Our findings indicated that TNFα induces hepatic MRP4 expression through activation of the p38-E2F1-Nrf2 signaling pathway in human obstructive cholestasis.
AuthorsWei Lian, Xiaocong Liu, Wensheng Chen
JournalYonsei medical journal (Yonsei Med J) Vol. 60 Issue 11 Pg. 1045-1053 (Nov 2019) ISSN: 1976-2437 [Electronic] Korea (South)
PMID31637886 (Publication Type: Journal Article)
Copyright© Copyright: Yonsei University College of Medicine 2019.
Chemical References
  • ABCC4 protein, human
  • Abcc4 protein, mouse
  • E2F1 Transcription Factor
  • Multidrug Resistance-Associated Proteins
  • NF-E2-Related Factor 2
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • p38 Mitogen-Activated Protein Kinases
Topics
  • Adult
  • Animals
  • Cholestasis (blood, genetics, metabolism, pathology)
  • Disease Models, Animal
  • Drug Resistance, Multiple
  • E2F1 Transcription Factor (metabolism)
  • Female
  • HEK293 Cells
  • Hep G2 Cells
  • Humans
  • Liver (metabolism)
  • Male
  • Mice, Inbred C57BL
  • Middle Aged
  • Models, Biological
  • Multidrug Resistance-Associated Proteins (metabolism)
  • NF-E2-Related Factor 2 (metabolism)
  • Promoter Regions, Genetic
  • Protein Binding
  • RNA, Messenger (genetics, metabolism)
  • Signal Transduction
  • Tumor Necrosis Factor-alpha (blood, metabolism)
  • p38 Mitogen-Activated Protein Kinases (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: