MedicineCell BiologyPharmacologyApoptosisRenal PathophysiologyRenal PharmacotherapyAcute Kidney InjuryRenal DiseaseRenal IschemiaRenal Ischemic InjuryRenal PharmacologyAcute Kidney Injury PathophysiologyAcute Kidney Injury PharmacotherapyCell Damage MechanismsG2 Phase RegulationP53 InactivationRenal ApoptosisRenal Tubular Epithelial RepairTubular Cell Repair
, cell damage was induced by addition of TNF-α, and then cells were treated with pifithrin-α. Cells treated with TNF-α alone in G2/M phase increased significantly, but they were reduced in the presence of pifithrin-α. In NRK-52E cells treated with pifithrin-α for 6 h, NGAL mRNA expression was significantly lower than in cells without pifithrin-α treatment. After NRK-52E cells were treated with pifithrin-α for 24 h, α-SMA and FN mRNA expression was significantly lower than in cells without the treatment. In summary, pifithrin-α can facilitate the progression of renal tubular epithelial cells through G2/M phase, protecting them against injury.
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Epithelial cell cycle arrest in G2/M mediates kidney fibrosis after injury
Li Yang, Tatiana Y. Besschetnova, Craig R. Brooks et al. · Nature Medicine · 2010 · 1.3K citations · Full text
Medicine, Cell Biology, Nephrology +14