Literature DB >> 2883191

Specific gene expression during compensatory renal hypertrophy in the rat.

D G Beer, K A Zweifel, D P Simpson, H C Pitot.   

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.

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Year:  1987        PMID: 2883191     DOI: 10.1002/jcp.1041310106

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  8 in total

Review 1.  Autocrine and paracrine mechanisms in the early stages of diabetic nephropathy.

Authors:  G Pugliese; F Pricci; G Romeo; G Leto; L Amadio; C Iacobini; U Di Mario
Journal:  J Endocrinol Invest       Date:  1999-10       Impact factor: 4.256

2.  Expression of two "immediate early" genes, Egr-1 and c-fos, in response to renal ischemia and during compensatory renal hypertrophy in mice.

Authors:  A J Ouellette; R A Malt; V P Sukhatme; J V Bonventre
Journal:  J Clin Invest       Date:  1990-03       Impact factor: 14.808

Review 3.  Cell pH and transepithelial H/HCO3 transport in the renal proximal tubule.

Authors:  R Krapf; R J Alpern
Journal:  J Membr Biol       Date:  1993-01       Impact factor: 1.843

4.  Expression of ras gene family as result of compensatory renal growth in mice.

Authors:  K Nomata; H Igarashi; H Kanetake; T Miyamoto; Y Saito
Journal:  Urol Res       Date:  1990

5.  Elevated c-myc protooncogene expression in autosomal recessive polycystic kidney disease.

Authors:  B D Cowley; F L Smardo; J J Grantham; J P Calvet
Journal:  Proc Natl Acad Sci U S A       Date:  1987-12       Impact factor: 11.205

6.  Patterns of mRNA expression during early cell growth differ in kidney epithelial cells destined to undergo compensatory hypertrophy versus regenerative hyperplasia.

Authors:  J T Norman; R E Bohman; G Fischmann; J W Bowen; A McDonough; D Slamon; L G Fine
Journal:  Proc Natl Acad Sci U S A       Date:  1988-09       Impact factor: 11.205

7.  Increased Na/H antiporter and Na/3HCO3 symporter activities in chronic hyperfiltration. A model of cell hypertrophy.

Authors:  P A Preisig; R J Alpern
Journal:  J Gen Physiol       Date:  1991-02       Impact factor: 4.086

8.  Unilateral Nephrectomy Stimulates ERK and Is Associated With Enhanced Na Transport.

Authors:  Robert Repetti; Nomrota Majumder; Karin Carneiro De Oliveira; Jennifer Meth; Tenzin Yangchen; Mukut Sharma; Tarak Srivastava; Rajeev Rohatgi
Journal:  Front Physiol       Date:  2021-02-03       Impact factor: 4.755

  8 in total

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