HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Fractalkine receptor (CX3CR1) inhibition is protective against ischemic acute renal failure in mice.

Abstract
Fractalkine (CX3CL1) is expressed on injured endothelial cells and is a potent chemoattractant and adhesion molecule for macrophages carrying the fractalkine receptor (CX3CR1). The aim of this study was to investigate the role of CX3CL1, and its ligand CX3CR1, in ischemic acute renal failure (ARF) in mice. On immunoblotting, CX3CL1 protein expression in the kidney increased markedly in ischemic ARF. On immunofluorescence staining, the intensity of CX3CL1 staining in blood vessels was significantly more prominent in ischemic ARF compared with controls. A specific anti-CX3CR1 antibody (25 microg i.p. 1 h before induction of ischemia) was functionally and histologically protective against ischemic ARF. CX3CR1 is predominantly expressed on macrophages. Macrophage infiltration in the kidney in ischemic ARF was significantly decreased after anti-CX3CR1 antibody treatment. To determine the role of macrophages in ischemic ARF, macrophages in the kidney were depleted using liposomal-encapsulated clodronate (LEC). LEC resulted in significant functional and histological protection against ischemic ARF. In summary, in ischemic ARF, 1) there is upregulation of CX3CL1 protein in the kidney, specifically in blood vessels; 2) CX3CR1 inhibition using a specific antibody is partially protective and is associated with reduced macrophage infiltration in the kidney; and 3) macrophage depletion in the kidney is protective.
AuthorsDong-Jin Oh, Belda Dursun, Zhibin He, Lawrence Lu, Thomas S Hoke, Danica Ljubanovic, Sarah Faubel, Charles L Edelstein
JournalAmerican journal of physiology. Renal physiology (Am J Physiol Renal Physiol) Vol. 294 Issue 1 Pg. F264-71 (Jan 2008) ISSN: 1931-857X [Print] United States
PMID18003857 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Antibodies, Anti-Idiotypic
  • CD11b Antigen
  • CX3C Chemokine Receptor 1
  • Chemokine CX3CL1
  • Cx3cl1 protein, mouse
  • Cx3cr1 protein, mouse
  • Receptors, Chemokine
  • Antimycin A
Topics
  • Acute Kidney Injury (metabolism, pathology, prevention & control)
  • Animals
  • Antibodies, Anti-Idiotypic (immunology, pharmacology)
  • Antimycin A (pharmacology)
  • CD11b Antigen (metabolism)
  • CX3C Chemokine Receptor 1
  • Cell Movement
  • Cells, Cultured
  • Chemokine CX3CL1 (physiology)
  • Disease Models, Animal
  • Endothelium, Vascular (drug effects, metabolism, pathology)
  • Kidney (metabolism, pathology)
  • Macrophages (immunology, pathology)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Receptors, Chemokine (antagonists & inhibitors, immunology, 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: