Expression and localization of ornithine decarboxylase in reversible papillomatosis induced by uracil in rat bladder
- PMID: 9617342
- PMCID: PMC5921823
- DOI: 10.1111/j.1349-7006.1998.tb00574.x
Expression and localization of ornithine decarboxylase in reversible papillomatosis induced by uracil in rat bladder
Abstract
Direct mechanical irritation by uracil calculi formed following feeding of 3% uracil in the diet to male rats produces severe papillary hyperplasia (papillomatosis, which is reversible) of bladder epithelium. To evaluate the mechanism of the appearance of uracil-induced papillomatosis, we examined the changes of the enzyme activity and the localization of ornithine decarboxylase (ODC), as well as polyamine biosynthesis, and epithelial proliferation, that accompany the sequential bladder epithelial changes following administration and withdrawal of uracil. Moreover, expression of ODC mRNA was investigated using northern blotting and localization of ODC mRNA was demonstrated using in situ hybridization. ODC activity during uracil administration was maintained at a high level compared to that in normal epithelium, but sharply decreased after cessation of uracil treatment. The accumulation of ODC protein was observed in the proliferating bladder epithelium by immunohistochemical examination and western blotting analysis, and even after cessation of treatment, the protein binding to anti-ODC antibody remained mildly elevated. Sequential changes of proliferating cell nuclear antigen (PCNA)-positive cells in the epithelium during the development and disappearance of papillomatosis correlated with ODC activity. ODC mRNA was expressed strongly in the proliferating epithelium in rats treated with uracil and weakly in normal epithelium, in accordance with the location of ODC protein. Consequently, our data demonstrate that cell proliferation in the development of papillomatosis is closely associated with polyamine metabolism, and moreover suggest that ODC activity is up-regulated at a post-translational step.
Similar articles
-
Spermidine/spermine N1-acetyltransferase, a new biochemical marker for epithelial proliferation in rat bladder.Jpn J Cancer Res. 1992 Oct;83(10):1037-40. doi: 10.1111/j.1349-7006.1992.tb02718.x. Jpn J Cancer Res. 1992. PMID: 1360468 Free PMC article.
-
Reversibility and apoptosis in rat urinary bladder papillomatosis induced by uracil.Carcinogenesis. 1997 Aug;18(8):1485-9. doi: 10.1093/carcin/18.8.1485. Carcinogenesis. 1997. PMID: 9276620
-
Uracil-induced urolithiasis and the development of reversible papillomatosis in the urinary bladder of F344 rats.Cancer Res. 1986 Apr;46(4 Pt 2):2062-7. Cancer Res. 1986. PMID: 3948181
-
Cell proliferation induced by uracil-calculi and subsequent development of reversible papillomatosis in the rat urinary bladder.Cancer Res. 1989 Jan 15;49(2):378-83. Cancer Res. 1989. PMID: 2910456
-
A new perspective on ornithine decarboxylase regulation: prevention of polyamine toxicity is the overriding theme.J Cell Biochem. 1991 Jun;46(2):102-5. doi: 10.1002/jcb.240460203. J Cell Biochem. 1991. PMID: 1918176 Review.
References
-
- ) Babaya , K. , Izumi , K. , Ozono , S. , Miyata , Y. , Morisawa , A. , Chmiel , J. S. and Oyasu , R.Capability of urinary components to enhance ornithine decarboxylase activity and promote urothelial tumorigenicity . Cancer Res. , 43 , 1774 – 1782 ( 1983. ). - PubMed
-
- ) O'Brien , T. G. , Simsiman , R. C. and Boutwell , R. K.Induction of the polyamine‐biosynthetic enzymes in mouse epidermis and their specificity for tumor promotion . Cancer Res. , 35 , 2426 – 2433 ( 1975. ). - PubMed
-
- ) Clayson , D. B.Bladder carcinogenesis in rat and mice: possibility of artifacts . J. Natl. Cancer Inst. , 52 , 1685 – 1689 ( 1974. ). - PubMed
-
- ) Toyoshima , K. and Leighton , J.Bladder calculi and urothelial hyperplasia with papillomatosis in the rat following insertion of chalk powder in the bladder cavity with subsequent trauma of the bladder wall . Cancer Res. , 35 , 3786 – 3791 ( 1975. ). - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous