Affiliation:
1. Wuhu Hospital East China Normal University Wuhu Anhui China
2. Health Science Center East China Normal University Shanghai China
3. Division of Nephrology Affiliated Hospital of Nantong University, Medical School of Nantong University Nantong Jiangsu China
4. Advanced Institute for Medical Sciences Dalian Medical University Dalian Liaoning China
Abstract
AbstractFarnesoid X receptor (FXR), a ligand‐activated transcription factor, plays an important role in maintaining water homeostasis by up‐regulating aquaporin 2 (AQP2) expression in renal medullary collecting ducts; however, its role in the survival of renal medullary interstitial cells (RMICs) under hypertonic conditions remains unclear. We cultured primary mouse RMICs and found that the FXR was expressed constitutively in RMICs, and that its expression was significantly up‐regulated at both mRNA and protein levels by hypertonic stress. Using luciferase and ChIP assays, we found a potential binding site of nuclear factor kappa‐B (NF‐κB) located in the FXR gene promoter which can be bound and activated by NF‐κB. Moreover, hypertonic stress‐induced cell death in RMICs was significantly attenuated by FXR activation but worsened by FXR inhibition. Furthermore, FXR increased the expression and nuclear translocation of hypertonicity‐induced tonicity‐responsive enhance‐binding protein (TonEBP), the expressions of its downstream target gene sodium myo‐inositol transporter (SMIT), and heat shock protein 70 (HSP70). The present study demonstrates that the NF‐κB/FXR/TonEBP pathway protects RMICs against hypertonic stress.