Blog
About

2
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Antibody to transforming growth factor-beta ameliorates tubular apoptosis in unilateral ureteral obstruction.

      Kidney International

      therapy, prevention & control, pathology, Ureteral Obstruction, analysis, Tumor Suppressor Protein p53, secretion, immunology, Transforming Growth Factor beta, Stress, Mechanical, Rats, Sprague-Dawley, Rats, Proto-Oncogene Proteins c-bcl-2, genetics, Proliferating Cell Nuclear Antigen, Nitric Oxide Synthase Type II, metabolism, Nitric Oxide Synthase, Nitric Oxide, Nephritis, Interstitial, enzymology, chemistry, Kidney Tubules, In Situ Nick-End Labeling, Gene Expression Regulation, Enzymologic, Fibrosis, Citrulline, Cell Line, Blotting, Western, Atrophy, Apoptosis, pharmacology, Antibodies, Monoclonal, Animals

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Unilateral ureteral obstruction (UUO) is characterized by progressive renal atrophy, renal interstitial fibrosis, an increase in renal transforming growth factor-beta (TGF-beta), and renal tubular apoptosis. The present study was undertaken to determine the effect of a monoclonal antibody to TGF-beta (1D11) in UUO. Mechanical stretch was applied to tubular epithelial cells (NRK-52E) by a computer-assisted system. Three doses of 1D11 (either 0.5, 2, or 4 mg/rat) were administered to rats one day prior to UUO and every two days thereafter, and kidneys were harvested at day 13. Fibrosis was assessed by measuring tissue hydroxyproline and mRNA for collagen and fibronectin. Apoptosis was assessed with the terminal deoxy transferase uridine triphosphate nick end-labeling assay. TGF-beta levels were determined by bioassay. Western blot and immunostaining were used to identify proliferating cell nuclear antigen (PCNA), p53, bcl-2, and inducible nitric oxide synthase (iNOS). Stretch significantly induced apoptosis in NRK-52E cells, which was accompanied by an increased release of TGF-beta; 1D11 (10 microg/mL) totally inhibited stretch-induced apoptosis. Control obstructed kidney contained 20-fold higher TGF-beta as compared with its unobstructed kidney; 1D11 neutralized tissue TGF-beta of the obstructed kidney. Control obstructed kidney exhibited significantly more fibrosis and tubular apoptosis than its unobstructed counterpart, which was blunted by 1D11. In contrast, 1D11 significantly increased tubular proliferation. p53 immunostaining was localized to renal tubular nuclei of control obstructed kidney and was diminished by 1D11. In contrast, bcl-2 was up-regulated in the 1D11-treated obstructed kidney. Total NOS activity and iNOS activity of the obstructed kidney were increased by 1D11 treatment. The present study strongly suggests that an antibody to TGF-beta is a promising agent to prevent renal tubular fibrosis and apoptosis in UUO.

          Related collections

          Author and article information

          Journal
          10.1046/j.1523-1755.2000.00414.x
          11115064

          Comments

          Comment on this article