Journal of the American Society of Nephrology · 1997 · 30 citations · 34 references
MedicineCell BiologyPharmacologyCell ProliferationInflammationRenal PathophysiologyAnimal Cell CultureExtracellular MatrixExtracellular Matrix BiologyExtracellular Matrix RemodelingGlomerular PathophysiologyRenal InflammationConstitutive Gene ExpressionGelatinase ActivityInhibitor SelectivityMatrix Metalloproteinase InhibitorsMatrix MetalloproteinasesMesangial Cell ProliferationMesangial ProliferationType Iv Collagen
The synthetic inhibitor of matrix metalloproteinases (MMP) Ro 31-9790, a hydroxamic-acid derivative, was investigated for its effect on rat mesangial cells (MC) in culture. For these studies, proliferating MC with a high degree of constitutive expression of a MMP, the 72-kD Type IV collagenase (gelatinase A, MMP-2), were chosen, because they reflect aspects of an inflammatory phenotype that may occur during certain forms of glomerular inflammatory diseases. Ro 31-9790 inhibited activity of the rat MC MMP-2 in a concentration-dependent and competitive fashion, as analyzed by quantitative densitometry and by a continuously recording fluorescent assay. Furthermore, Ro 31-9790 inhibited the proliferation rate of cultured rat MC in a concentration-dependent and at least partially reversible manner without affecting cell viability. It was concluded that the application of synthetic MMP inhibitors may offer a new perspective for the therapy of mesangial cell-derived forms of glomerulonephritis.
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