Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1994 Jan 4;91(1):148–152. doi: 10.1073/pnas.91.1.148

Role of adrenal renin in the regulation of adrenal steroidogenesis by corticotropin.

M Sander 1, D Ganten 1, S H Mellon 1
PMCID: PMC42903  PMID: 8278356

Abstract

The major regulator of mineralocorticoid production in the adrenal is angiotensin II produced by the action of renal renin. The discovery that the rodent adrenal also synthesizes renin and angiotensinogen suggests there is autocrine regulation of mineralocorticoid synthesis. The transgenic rat [TGR(mREN2)27] expresses the Ren-2d gene predominantly in the adrenal. Despite suppressed kidney and plasma renin, these animals develop fulminant hypertension between 5 and 15 weeks of age. Corticosteroid concentrations are significantly elevated during hypertension development. We assessed steroidogenesis in TGR(mREN2)27 rats by analyzing the expression of the mRNAs for three steroidogenic enzymes: P450scc, the rate-limiting step of steroidogenesis; P450c11 beta, which converts deoxycorticosterone to corticosterone in the zona fasciculata/reticularis; and P450c11AS, which converts deoxycorticosterone to aldosterone in the zona glomerulosa. P450c11AS mRNA, but neither P450c11 beta nor P450scc mRNA, was overexpressed in the adrenal gland of TGR(mREN2)27 rats. In situ hybridization with specific probes for P450c11 beta and P450c11AS mRNA localized the former exclusively to the zona fasciculata and the latter to the zona glomerulosa. In TGR(mREN2)27 rats, the size of the adrenal and number of P450c11AS-expressing zona glomerulosa cells were about twice those of a normal Sprague-Dawley rat. Both animals respond to corticotropin similarly; corticotropin had no effect on the expression of P450scc and P45011 beta mRNAs, rendered P450c11AS mRNA undetectable, and simultaneously altered the morphology of the adrenal cortex, resulting in a lack of zona glomerulosa-like cells. Thus, the local renin-angiotensin system has a major effect on the basal expression of P450c11AS mRNA, but little effect on the corticotropin-regulated expression of P450scc, P450c11 beta, and P450c11AS mRNAs.

Full text

PDF
148

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Aguilera G., Catt K. J. Loci of action of regulators of aldosterone biosynthesis in isolated glomerulosa cells. Endocrinology. 1979 Apr;104(4):1046–1052. doi: 10.1210/endo-104-4-1046. [DOI] [PubMed] [Google Scholar]
  2. Aguilera G., Fujita K., Catt K. J. Mechanisms of inhibition of aldosterone secretion by adrenocorticotropin. Endocrinology. 1981 Feb;108(2):522–528. doi: 10.1210/endo-108-2-522. [DOI] [PubMed] [Google Scholar]
  3. Bachmann S., Peters J., Engler E., Ganten D., Mullins J. Transgenic rats carrying the mouse renin gene--morphological characterization of a low-renin hypertension model. Kidney Int. 1992 Jan;41(1):24–36. doi: 10.1038/ki.1992.4. [DOI] [PubMed] [Google Scholar]
  4. Bader M., Zhao Y., Sander M., Lee M. A., Bachmann J., Böhm M., Djavidani B., Peters J., Mullins J. J., Ganten D. Role of tissue renin in the pathophysiology of hypertension in TGR(mREN2)27 rats. Hypertension. 1992 Jun;19(6 Pt 2):681–686. doi: 10.1161/01.hyp.19.6.681. [DOI] [PubMed] [Google Scholar]
  5. Barrett P. Q., Bollag W. B., Isales C. M., McCarthy R. T., Rasmussen H. Role of calcium in angiotensin II-mediated aldosterone secretion. Endocr Rev. 1989 Nov;10(4):496–518. doi: 10.1210/edrv-10-4-496. [DOI] [PubMed] [Google Scholar]
  6. Boggaram V., Zuber M. X., Waterman M. R. Turnover of newly synthesized cytochromes P-450scc and P-45011 beta and adrenodoxin in bovine adrenocortical cells in monolayer culture: effect of adrenocorticotropin. Arch Biochem Biophys. 1984 Jun;231(2):518–523. doi: 10.1016/0003-9861(84)90416-8. [DOI] [PubMed] [Google Scholar]
  7. Campbell D. J., Habener J. F. Angiotensinogen gene is expressed and differentially regulated in multiple tissues of the rat. J Clin Invest. 1986 Jul;78(1):31–39. doi: 10.1172/JCI112566. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Deschepper C. F., Mellon S. H., Cumin F., Baxter J. D., Ganong W. F. Analysis by immunocytochemistry and in situ hybridization of renin and its mRNA in kidney, testis, adrenal, and pituitary of the rat. Proc Natl Acad Sci U S A. 1986 Oct;83(19):7552–7556. doi: 10.1073/pnas.83.19.7552. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Di Blasio A. M., Voutilainen R., Jaffe R. B., Miller W. L. Hormonal regulation of messenger ribonucleic acids for P450scc (cholesterol side-chain cleavage enzyme) and P450c17 (17 alpha-hydroxylase/17,20-lyase) in cultured human fetal adrenal cells. J Clin Endocrinol Metab. 1987 Jul;65(1):170–175. doi: 10.1210/jcem-65-1-170. [DOI] [PubMed] [Google Scholar]
  10. Ganten D., Hutchinson J. S., Schelling P., Ganten U., Fischer H. The iso-renin angiotensin systems in extrarenal tissue. Clin Exp Pharmacol Physiol. 1976 Mar-Apr;3(2):103–126. doi: 10.1111/j.1440-1681.1976.tb00596.x. [DOI] [PubMed] [Google Scholar]
  11. Gill G. N., Ill C. R., Simonian M. H. Angiotensin stimulation of bovine adrenocortical cell growth. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5569–5573. doi: 10.1073/pnas.74.12.5569. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hall P. F., Charpponnier C., Nakamura M., Gabbiani G. The role of microfilaments in the response of adrenal tumor cells to adrenocorticotropic hormone. J Biol Chem. 1979 Sep 25;254(18):9080–9084. [PubMed] [Google Scholar]
  13. Hornsby P. J., O'Hare M. J., Neville A. M. Functional and morphological observations on rat adrenal zona glomerulosa cells in monolayer culture. Endocrinology. 1974 Nov;95(5):1240–1251. doi: 10.1210/endo-95-5-1240. [DOI] [PubMed] [Google Scholar]
  14. John M. E., John M. C., Simpson E. R., Waterman M. R. Regulation of cytochrome P-45011 beta gene expression by adrenocorticotropin. J Biol Chem. 1985 May 10;260(9):5760–5767. [PubMed] [Google Scholar]
  15. Lauber M., Böni-Schnetzler M., Müller J. Potassium raises cytochrome P-45011 beta mRNA level in zona glomerulosa of rat adrenals. Mol Cell Endocrinol. 1990 Sep 10;72(3):159–166. doi: 10.1016/0303-7207(90)90140-4. [DOI] [PubMed] [Google Scholar]
  16. Lauber M., Muller J. Purification and characterization of two distinct forms of rat adrenal cytochrome P450(11) beta: functional and structural aspects. Arch Biochem Biophys. 1989 Oct;274(1):109–119. doi: 10.1016/0003-9861(89)90421-9. [DOI] [PubMed] [Google Scholar]
  17. Malee M. P., Mellon S. H. Zone-specific regulation of two messenger RNAs for P450c11 in the adrenals of pregnant and nonpregnant rats. Proc Natl Acad Sci U S A. 1991 Jun 1;88(11):4731–4735. doi: 10.1073/pnas.88.11.4731. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Marusic E. T., Mulrow P. J. In vitro conversion of corticosterone-4-14-C to 18-hydroxycorticosterone by zona fasciuculata-reticularis of beef adrenal. Endocrinology. 1967 Jan;80(1):214–218. doi: 10.1210/endo-80-1-214. [DOI] [PubMed] [Google Scholar]
  19. Matsukawa N., Nonaka Y., Ying Z., Higaki J., Ogihara T., Okamoto M. Molecular cloning and expression of cDNAS encoding rat aldosterone synthase: variants of cytochrome P-450(11 beta). Biochem Biophys Res Commun. 1990 May 31;169(1):245–252. doi: 10.1016/0006-291x(90)91460-a. [DOI] [PubMed] [Google Scholar]
  20. Mazzocchi G., Malendowicz L. K., Rebuffat P., Robba C., Gottardo G., Nussdorfer G. G. Short- and long-term effects of ACTH on the adrenal zona glomerulosa of the rat. A coupled stereological and enzymological study. Cell Tissue Res. 1986;243(2):303–310. doi: 10.1007/BF00251044. [DOI] [PubMed] [Google Scholar]
  21. Mellon S. H., Kushner J. A., Vaisse C. Expression and regulation of adrenodoxin and P450scc mRNA in rodent tissues. DNA Cell Biol. 1991 Jun;10(5):339–347. doi: 10.1089/dna.1991.10.339. [DOI] [PubMed] [Google Scholar]
  22. Mellon S. H., Miller W. L. Extraadrenal steroid 21-hydroxylation is not mediated by P450c21. J Clin Invest. 1989 Nov;84(5):1497–1502. doi: 10.1172/JCI114325. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Miller W. L. Molecular biology of steroid hormone synthesis. Endocr Rev. 1988 Aug;9(3):295–318. doi: 10.1210/edrv-9-3-295. [DOI] [PubMed] [Google Scholar]
  24. Mullins J. J., Peters J., Ganten D. Fulminant hypertension in transgenic rats harbouring the mouse Ren-2 gene. Nature. 1990 Apr 5;344(6266):541–544. doi: 10.1038/344541a0. [DOI] [PubMed] [Google Scholar]
  25. Müller J., Meuli C., Schmid C., Lauber M. Adaptation of aldosterone biosynthesis to sodium and potassium intake in the rat. J Steroid Biochem. 1989;34(1-6):271–277. doi: 10.1016/0022-4731(89)90091-5. [DOI] [PubMed] [Google Scholar]
  26. Nonaka Y., Matsukawa N., Morohashi, Omura T., Ogihara T., Teraoka H., Okamoto M. Molecular cloning and sequence analysis of cDNA encoding rat adrenal cytochrome P-450(11)beta. FEBS Lett. 1989 Sep 11;255(1):21–26. doi: 10.1016/0014-5793(89)81053-1. [DOI] [PubMed] [Google Scholar]
  27. Nudel U., Zakut R., Shani M., Neuman S., Levy Z., Yaffe D. The nucleotide sequence of the rat cytoplasmic beta-actin gene. Nucleic Acids Res. 1983 Mar 25;11(6):1759–1771. doi: 10.1093/nar/11.6.1759. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Ogishima T., Mitani F., Ishimura Y. Isolation of aldosterone synthase cytochrome P-450 from zona glomerulosa mitochondria of rat adrenal cortex. J Biol Chem. 1989 Jul 5;264(19):10935–10938. [PubMed] [Google Scholar]
  29. Ogishima T., Suzuki H., Hata J., Mitani F., Ishimura Y. Zone-specific expression of aldosterone synthase cytochrome P-450 and cytochrome P-45011 beta in rat adrenal cortex: histochemical basis for the functional zonation. Endocrinology. 1992 May;130(5):2971–2977. doi: 10.1210/endo.130.5.1572304. [DOI] [PubMed] [Google Scholar]
  30. Pedersen R. C., Brownie A. C., Ling N. Pro-adrenocorticotropin/endorphin-derived peptides: coordinate action on adrenal steroidogenesis. Science. 1980 May 30;208(4447):1044–1046. doi: 10.1126/science.6246578. [DOI] [PubMed] [Google Scholar]
  31. Sander M., Bader M., Djavidani B., Maser-Gluth C., Vecsei P., Mullins J., Ganten D., Peters J. The role of the adrenal gland in hypertensive transgenic rat TGR(mREN2)27. Endocrinology. 1992 Aug;131(2):807–814. doi: 10.1210/endo.131.2.1322284. [DOI] [PubMed] [Google Scholar]
  32. Shibata H., Ogishima T., Mitani F., Suzuki H., Murakami M., Saruta T., Ishimura Y. Regulation of aldosterone synthase cytochrome P-450 in rat adrenals by angiotensin II and potassium. Endocrinology. 1991 May;128(5):2534–2539. doi: 10.1210/endo-128-5-2534. [DOI] [PubMed] [Google Scholar]
  33. Simpson E. R., McCarthy J. L., Peterson J. A. Evidence that the cycloheximide-sensitive site of adrenocorticotropic hormone action is in the mitochondrion. Changes in pregnenolone formation, cholesterol content, and the electron paramagnetic resonance spectra of cytochrome P-450. J Biol Chem. 1978 May 10;253(9):3135–3139. [PubMed] [Google Scholar]
  34. Townsend S. F., Dallman M. F., Miller W. L. Rat insulin-like growth factor-I and -II mRNAs are unchanged during compensatory adrenal growth but decrease during ACTH-induced adrenal growth. J Biol Chem. 1990 Dec 25;265(36):22117–22122. [PubMed] [Google Scholar]
  35. Tremblay A., Parker K. L., Lehoux J. G. Dietary potassium supplementation and sodium restriction stimulate aldosterone synthase but not 11 beta-hydroxylase P-450 messenger ribonucleic acid accumulation in rat adrenals and require angiotensin II production. Endocrinology. 1992 Jun;130(6):3152–3158. doi: 10.1210/endo.130.6.1597135. [DOI] [PubMed] [Google Scholar]
  36. Yamaguchi T., Naito Z., Stoner G. D., Franco-Saenz R., Mulrow P. J. Role of the adrenal renin-angiotensin system on adrenocorticotropic hormone- and potassium-stimulated aldosterone production by rat adrenal glomerulosa cells in monolayer culture. Hypertension. 1990 Dec;16(6):635–641. doi: 10.1161/01.hyp.16.6.635. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES