Specific gene expression during compensatory renal hypertrophy in the rat

J Cell Physiol. 1987 Apr;131(1):29-35. doi: 10.1002/jcp.1041310106.

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.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • DNA / biosynthesis
  • Hypertrophy / metabolism*
  • Kidney / enzymology
  • Kidney / growth & development
  • Kidney / pathology
  • Male
  • Nephrectomy / methods
  • Ornithine-Oxo-Acid Transaminase / metabolism
  • Proto-Oncogenes
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Inbred Strains
  • Regeneration
  • Time Factors
  • Transcription, Genetic*
  • gamma-Glutamyltransferase / metabolism

Substances

  • RNA, Messenger
  • DNA
  • gamma-Glutamyltransferase
  • Ornithine-Oxo-Acid Transaminase