Literature DB >> 4087690

Tubular basement membrane changes in 2-amino-4,5-diphenylthiazole-induced polycystic disease.

R J Butkowski, F A Carone, J J Grantham, B G Hudson.   

Abstract

Polycystic renal disease was induced in rats by feeding 2-amino-4,5-diphenylthiazole. Tubular (TBM) and glomerular basement membranes (GBM) were purified and analyzed for possible structural changes that may be a factor in the development of the tubular dilations and cysts. Changes in the relative quantities of TBM polypeptides were detected by sodium dodecylsulfate polyacrylamide gel electrophoresis. An overall increase in the concentration of high molecular weight components and a decrease in concentration of those of low molecular weight components were observed. Changes which were particularly notable included a twofold increase in a component of Mr = 380,000 and a decrease in one of Mr = 55,000 as analyzed without reduction of disulfide bonds. With reduction of disulfide bonds, the Mr = 380,000 component dissociates, whereas the Mr = 55,000 polypeptide does not, and polypeptides of Mr = 245,000 and 145,000 are observed to does not, and polypeptides of Mr = 245,000 and 145,000 are observed to increase about twofold in concentration (approximate molecular weights were determined using globular protein standards). These changes take place most rapidly from 4 to 8 weeks of drug administration and remain relatively constant between 8 and 16 weeks. If feeding of the drug is discontinued, the distribution of TBM polypeptides returns to normal. These results indicate that tubular basement membrane from animals with 2-amino-4,5-diphenylthiazole-induced polycystic renal disease is abnormal, and this should be considered as a possible contributing factor in the formation of cysts.

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Year:  1985        PMID: 4087690     DOI: 10.1038/ki.1985.193

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  6 in total

1.  Metal-inducible pathology in the liver, pancreas, and kidney of transgenic mice expressing SV40 early region genes.

Authors:  K R Dyer; A Messing
Journal:  Am J Pathol       Date:  1989-08       Impact factor: 4.307

Review 2.  Epithelial hyperplasia in human polycystic kidney diseases. Its role in pathogenesis and risk of neoplasia.

Authors:  J Bernstein; A P Evan; K D Gardner
Journal:  Am J Pathol       Date:  1987-10       Impact factor: 4.307

3.  Comparison of the morphology of renal cysts and cystic renal tumors.

Authors:  Judit Kovács; Szabolcs Gomba; Mónika Zilahy
Journal:  Pathol Oncol Res       Date:  1997       Impact factor: 3.201

4.  Basement membrane antigens in renal polycystic disease.

Authors:  F A Carone; H Makino; Y S Kanwar
Journal:  Am J Pathol       Date:  1988-03       Impact factor: 4.307

5.  Tubular dilatation in the repair process of ischaemic tubular necrosis.

Authors:  A Shimizu; Y Masuda; M Ishizaki; Y Sugisaki; N Yamanaka
Journal:  Virchows Arch       Date:  1994       Impact factor: 4.064

6.  Congenital murine polycystic kidney disease. II. Pathogenesis of tubular cyst formation.

Authors:  E D Avner; W E Sweeney; M C Young; D Ellis
Journal:  Pediatr Nephrol       Date:  1988-04       Impact factor: 3.714

  6 in total

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