Specific gene expression during compensatory renal hypertrophy in the rat
- PMID: 2883191
- DOI: 10.1002/jcp.1041310106
Specific gene expression during compensatory renal hypertrophy in the rat
Abstract
The compensatory growth of the kidney which is induced by unilateral nephrectomy is a highly regulated process resulting principally in hypertrophy of the remaining kidney. The events which regulate this process are unknown. We have examined the levels of transcripts for the proto-oncogenes, myc, H-ras, K-ras, and fos, and the cellular genes, H4 histone, ornithine aminotransferase, and gamma-glutamyl transpeptidase, following unilateral nephrectomy in the rat. The pattern of expression of c-myc, c-H-ras, and c-K-ras during compensatory growth of the kidney differs from the pattern of expression of these proto-oncogenes during liver regeneration, in which, unlike the kidney, hyperplasia rather than hypertrophy predominates. The lack of change in the abundance of these proto-oncogene transcripts following unilateral nephrectomy suggests a primary relationship between the expression of these proto-oncogenes and DNA synthesis and indicates there may be separate signals for cell growth, one to double cell size and one to replicate DNA. Increased mRNA transcripts for the enzymes ornithine aminotransferase and gamma-glutamyl transpeptidase were induced in the contralateral kidney after nephrectomy. The time course of expression for these two enzymes differs. The early expression of the gamma-glutamyl transpeptidase gene may indicate an involvement of this glutathione-metabolizing enzyme during renal compensatory growth, while the function of the delayed increase in ornithine aminotransferase transcripts in the remaining kidney is not apparent.
Similar articles
-
Stimulation of renal and hepatic c-myc and c-Ha-ras expression by unilateral nephrectomy.Oncogene Res. 1990;5(4):287-93. Oncogene Res. 1990. PMID: 2204021
-
Messenger RNA for enzymes of ornithine and polyamine metabolism are selectively underexpressed in kidney of 5/6 nephrectomized rats.Exp Nephrol. 1997 Jul-Aug;5(4):285-94. Exp Nephrol. 1997. PMID: 9259182
-
Sequential protooncogene expression during rat liver regeneration.Cancer Res. 1986 Jun;46(6):3111-7. Cancer Res. 1986. PMID: 3516391
-
Macromolecular metabolism in compensatory renal hypertrophy.Yale J Biol Med. 1978 May-Jun;51(3):419-28. Yale J Biol Med. 1978. PMID: 366927 Free PMC article. Review.
-
Mesangial cells initiate compensatory tubular cell hypertrophy.Am J Nephrol. 2010;31(4):326-31. doi: 10.1159/000287229. Epub 2010 Feb 17. Am J Nephrol. 2010. PMID: 20160436 Review.
Cited by
-
Expression of two "immediate early" genes, Egr-1 and c-fos, in response to renal ischemia and during compensatory renal hypertrophy in mice.J Clin Invest. 1990 Mar;85(3):766-71. doi: 10.1172/JCI114502. J Clin Invest. 1990. PMID: 2107209 Free PMC article.
-
Increased Na/H antiporter and Na/3HCO3 symporter activities in chronic hyperfiltration. A model of cell hypertrophy.J Gen Physiol. 1991 Feb;97(2):195-217. doi: 10.1085/jgp.97.2.195. J Gen Physiol. 1991. PMID: 1849958 Free PMC article.
-
Patterns of mRNA expression during early cell growth differ in kidney epithelial cells destined to undergo compensatory hypertrophy versus regenerative hyperplasia.Proc Natl Acad Sci U S A. 1988 Sep;85(18):6768-72. doi: 10.1073/pnas.85.18.6768. Proc Natl Acad Sci U S A. 1988. PMID: 3413124 Free PMC article.
-
Autocrine and paracrine mechanisms in the early stages of diabetic nephropathy.J Endocrinol Invest. 1999 Oct;22(9):708-35. doi: 10.1007/BF03343635. J Endocrinol Invest. 1999. PMID: 10595837 Review. No abstract available.
-
Cell pH and transepithelial H/HCO3 transport in the renal proximal tubule.J Membr Biol. 1993 Jan;131(1):1-10. doi: 10.1007/BF02258529. J Membr Biol. 1993. PMID: 8381871 Review. No abstract available.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous