Life SciencesCell BiologyMolecular BiologyApoptosisRenal PathologyRenal PathophysiologyAcute Kidney InjuryDeath ReceptorsMicrorna BiologyRenal DiseaseRenal IschemiaRenal Ischemic InjuryApoptosis In Renal CellsApoptosis-regulating MicrornasBiomarkers Of Ischemic InjuryIschemic Organ InjuryMicrorna In ApoptosisMicrorna Regulation Of ApoptosisRenal ApoptosisRenal Tissue Injury
BACKGROUND: Ischemic reperfusion injury of kidney is major cause for renal failure, however the involved pathogenesis remains unclear creating an void for its effective treatment. Here we studied involvement of microRNA-424 in renal injury. METHODS: studies. Hoechst 33342 analysis was done for apoptosis. Blood urea nitrogen (BUN) and serum creatinine was done for renal function, Hematoxylin-eosin tissue damage and Terminal transferase-dUTP nick-end labeling assay for apoptosis. RT-PCR was done for miRNA and ChIP assay to identify the binding of p53 to miR-424. TargetScan and miRanda data base were scanned to find targets of miR-424. Protein expression was done by western blot analysis. RESULTS: . CONCLUSION: The study confirmed p53/miR-424/DR6 as a protective cascade during ischemic-reperfusion injury.
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Nandini D.P.K. Manne, Ravikumar Arvapalli, Vincent Graffeo et al. · Cellular Physiology and Biochemistry · 2017 · 705 citations · Full text