Journal of the American Society of Nephrology · 2005 · 108 citations · 32 references
MedicineNephrologyPharmacologyGene ExpressionMolecular PharmacologyRenal PathophysiologyRenal DiseaseRenal Drug DistributionRenal PharmacologyPromoter Activity AnalysisPromoter Activity AssaysRenal DrugsRenal TargetingTargeted Molecular TherapyTherapeutic Gene SilencingTranscriptional Gene Silencing
Pyrrole-imidazole (Py-Im) polyamides are nuclease-resistant novel compounds that inhibit gene expression by binding to the minor groove of DNA. A Py-Im polyamide that targets rat TGF-beta1 was designed as a gene-silencing agent for progressive renal diseases, and the distribution and the effects of this polyamide on renal injury were examined in Dahl-salt sensitive (Dahl-S) rats. For identification of transcription factor binding elements for activation of the rat TGF-beta1 gene, recombinant TGF-beta1 reporter plasmids were transfected into HEK-293 cells, and promoter activity was measured. Py-Im polyamide was designed to the activator protein-1 binding site of the rat TGF-beta1 promoter. This Py-Im polyamide showed strong, fast, and specific binding to the target DNA in gel mobility shift and Biacore assays. Py-Im polyamide significantly inhibited TGF-beta1 promoter activity and expression of TGF-beta1 mRNA and protein in rat mesangial cells. Intravenously administered fluorescein-labeled polyamide distributed to the kidney of rats. Py-Im polyamide significantly inhibited expression of TGF-beta1 mRNA and protein in the renal cortex of Dahl-S rats and reduced the increase in urinary protein and albumin in Dahl-S rats independent of changes in blood pressure. These results indicate that Py-Im polyamide that targets TGF-beta1 will be a novel gene-silencing agent for the TGF-beta1-associated diseases, including progressive renal diseases.
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Expression of transforming growth factor-β isoforms in human glomerular diseases
Tatsuo Yamamoto, Nancy A. Noble, Arthur H. Cohen et al. · Kidney International · 1996 · 420 citations