Horm Metab Res 2010; 42(12): 840-845
DOI: 10.1055/s-0030-1265129
Original Basic

© Georg Thieme Verlag KG Stuttgart · New York

The Effects of the Endothelium on Adrenal Steroidogenesis and Growth are Mainly Mediated by Proteins Other than Endothelin-1

I. Paramonova1 , 2 , M. Haase1 , B. Mülders-Opgenoorth1 , I. Ansurudeen-Rafi3 , S. R. Bornstein4 , C. Papewalis1 , S. Schinner1 , M. Schott1 , W. A. Scherbaum1 , H. S. Willenberg1
  • 1Department of Endocrinology, Diabetes and Rheumatology, University Hospital Düsseldorf, Düsseldorf, Germany
  • 2Department of Neurology, Krankenhaus Nordwest, Frankfurt, Germany
  • 3Department of Neuroscience, Karolinska Institute, Stockholm, Sweden
  • 4Department of Medicine III, Carl Gustav Carus Medical School, University of Technology, Dresden, Germany
Further Information

Publication History

received 12.06.2010

accepted 10.08.2010

Publication Date:
13 September 2010 (online)

Abstract

The endothelium releases factors stimulating the adrenal cortex. It is also known that endothelin-1 (ET-1) promotes generation of cortisol and aldosterone, and proliferation of adrenocortical cells. The aim of the study was to find out whether the effect of the endothelium on adrenocortical cells is dominated by the action of ET-1. The effects of endothelial cell-conditioned medium (ECCM), obtained during growth of human umbilical cord vein endothelial cells, on aldosterone and cortisol release by cells of the adrenocortical cancer cell-line NCI-H295R and the promoter activity of steroidogenic acute-regulatory protein (StAR) were studied. The effect of ECCM on proliferation of human primary normal adrenocortical and NCI-H295R cells was also investigated. Concentration-dependent increases in cortisol release that reached 192.7±62.8 in percent of basal secretion, in aldosterone release that reached 188.2±52.3 in percent of basal secretion, and in proliferation after stimulation with ECCM at concentrations of 10–50% were found. ECCM significantly activated the StAR promoter 3-fold in NCI-H295R cells if the ECCM was not pretreated with pronase. These effects of the endothelium were not reversed after co-incubation with endothelin receptor antagonists and could not be mimicked by incubation with endothelin-1. In conclusion, the cultured endothelial cells secrete a protein that stimulates steroidogenesis in adrenal cells and their growth. It was also shown that the ET-1 does not mediate the effect of ECCM on the NCI-H295R cell line.

References

  • 1 Sapirstein LA, Goldman HA. Adrenal blood flow in the albino rat.  Am J Physiol. 1959;  196 159-162
  • 2 Vinson GP, Pudney JA, Whitehouse BJ. The mammalian adrenal circulation and the relationship between adrenal blood flow and steroidogenesis.  Endocrinology. 1985;  105 285-294
  • 3 Dobbie JW, Symington T. The human adrenal gland with special reference to the vasculature.  J Endocrinol. 1991;  34 479-489
  • 4 Delarue C, Conlon JM, Remy-Jouet I, Fournier A, Vaudry H. Endothelins as local activators of adrenocortical cells.  J Mol Endocrinol. 2004;  32 1-7
  • 5 Lacroix A, N’Diaye N, Tremblay J, Hamet P. Ectopic and abnormal hormone receptors in adrenal Cushing's syndrome.  Endocr Rev. 2001;  22 75-110
  • 6 Willenberg HS, Stratakis CA, Marx C, Ehrhart-Bornstein M, Chrousos GP, Bornstein SR. Aberrant interleukin-1 receptors in a cortisol-secreting adrenal adenoma causing Cushing's syndrome.  N Engl J Med. 1998;  339 27-31
  • 7 Willenberg HS, Haase M, Papewalis C, Schott M, Scherbaum WA, Bornstein SR. Corticotropin-releasing hormone (CRH) receptor expression on normal and tumorous human adrenocortical cells.  Neuroendocrinology. 2005;  82 274-281
  • 8 Mazzuco TL, Lampron A, Bourdeau I, Lacroix A. Aberrant hormone receptors in primary aldosteronism.  Horm Metab Res. 2010;  42 416-423
  • 9 Hinson JP, Kapas S. The role of endothelial cell products in the regulation of adrenocortical function: actions of endothelin, nitric oxide, adrenomedullin and PAMP.  Horm Metab Res. 1998;  30 334-340
  • 10 Rossi GP, Belloni AS, Nussdorfer GG, Pessina AC. Endothelin-1 and the adrenal gland.  J Cardiovasc Pharmacol. 2000;  35 S17-S20
  • 11 Willenberg HS, Schinner S, Ansurudeen I. New mechanisms to control aldosterone synthesis.  Horm Metab Res. 2008;  40 435-441
  • 12 Rosolowsky LJ, Campbell WB. Endothelial cells stimulate aldosterone release from bovine adrenal glomerulosa cells.  Am J Physiol (Endocrinol Metab 29). 1994;  266 E107-E117
  • 13 Rosolowsky LJ, Hanke CJ, Campbell WB. Adrenal capillary endothelial cells stimulate aldosterone release through a protein that is distinct from endothelin.  Endocrinology. 1999;  140 4411-4418
  • 14 Ansurudeen I, Kopprasch S, Ehrhart-Bornstein M, Willenberg HS, Funk RHW, Krug AW, Bornstein SR. Vascular-adrenal niche – endothelial cell-mediated sensitization of human adrenocortical cells to angiotensin II.  Horm Metab Res. 2006;  38 476-480
  • 15 Ansurudeen I, Kopprasch S, Ehrhart-Bornstein M, Bornstein SR, Willenberg HS. Endothelial cell-mediated regulation of aldosterone release from human adrenocortical cells.  Mol Cell Endocrinol. 2007;  265–266 150-156
  • 16 Willenberg HS, Ansurudeen I, Schebesta K, Haase M, Wess B, Schinner S, Raffel A, Schott M, Scherbaum WA. The endothelium secretes interleukin-6 (IL-6) and induces adrenal IL-6 generation that does not interfere with the effect of endothelial cells on aldosterone synthesis.  Exp Clin Endocr Diab. 2008;  116 S70-S74
  • 17 Ansurudeen I, Willenberg HS, Kopprasch S, Ehrhart-Bornstein M, Bornstein SR. Endothelial factors mediate aldosterone release via PKA-independent pathways.  Mol Cell Endocrinol. 2009;  300 66-70
  • 18 Hinson JP, Kapas S, Teja R, Vinson GP. Effect of the endothelins on aldosterone secretion by rat zona glomerulosa cells in vitro.  J Steroid Biochem Mol Biol. 1991;  40 43743-43749
  • 19 Nussdorfer GG, Rossi GP, Belloni AS. The role of endothelins in the paracrine control of the secretion and growth of the adrenal cortex.  Int Rev Cytology. 1997;  171 267-308
  • 20 Mazzocchi G, Rossi GP, Rebuffat P, Malendowicz LK, Markowska A, Nussdorfer GG. Endothelin-1 stimulates deoxyribonucleic acid synthesis and cell proliferation in rat adrenal zona glomerulosa, acting through an endothelin A receptor coupled with protein kinase C- and tyrosine kinase-dependent signaling pathways.  Endocrinology. 1997;  138 2333-2338
  • 21 Rossi GP, Albertin G, Neri G, Andreis PG, Hofmann S, Pessina AC, Nussdorfer GG. Endothelin-1 stimulates steroid secretion of human adrenocortical cells ex vivo via both ETA and ETB receptor subtypes.  J Clin Endocrinol Metab. 1997;  82 3445-3449
  • 22 Korth P, Bohle RM, Corvol P, Pine F. Cellular distribution of endothelin-converting enzyme-1 in human tissues.  J Histochem Cytochem. 1999;  47 447-461
  • 23 Haase M, Ansurudeen I, Paramonova I, Schinner S, Schott M, Papewalis C, Scherbaum WA, Willenberg HS. Evidence for the involvement of endothelial cell products in adrenal CITED2 expression.  Cell Tissue Res. 2009;  336 337-343
  • 24 Caron KM, Ikeda Y, Soo SC, Stocco DM, Parker KL, Clark BJ. Characterization of the promoter region of the mouse gene encoding the steroidogenic acute regulatory protein.  Mol Endocrinol. 1997;  11 138-147
  • 25 Song S, Cooperman J, Letting DL, Blobel GA, Choi JK. Identification of cyclin D3 as a direct target of E2A using DamID.  Mol Cell Biol. 2004;  24 8790-8802
  • 26 Miller WL, Redfield MM, Burnett Jr JC. Integrated cardiac, renal, and endocrine actions of endothelin.  J Clin Invest. 1989;  83 317-320
  • 27 Rossi GP, Albertin G, Belloni A, Zanin L, Biasolo MA, Prayer-Galetti T, Bader M, Nussdorfer GG, Palù G, Pessina AC. Gene expression, localization, and characterization of endothelin A and B receptors in the human adrenal cortex.  J Clin Invest. 1994;  94 1226-1234
  • 28 Belloni AS, Pacheco YG, Markowska A, Andreis PG, Meneghelli V, Malendowicz LK, Nussdorfer GG. Distribution and functional significance of the endothelin receptor subtypes in the rat adrenal gland.  Cell Tissue Res. 1997;  288 345-352
  • 29 Zeng Z, Tang X, Yang D, Li H, Zhang R, Zeng Q, Li M, Chen J, Lu Z, Demura H, Naruse M, Shi Y. Immunoreactive endothelin-1 and its receptors in human adrenal tissues.  J Cardiovasc Pharmacol. 1998;  31 S212-S214
  • 30 Hinson JP, Vinson GP, Kapas S, Teja R. The role of endothelin in the control of adrenocortical function: stimulation of endothelin release by ACTH and the effects of endothelin-1 and endothelin-3 on steroidogenesis in rat and human adrenocortical cells.  J Endocrinol. 1991;  128 275-280
  • 31 Morishita R, Higaki J, Ogihara T. Endothelin stimulates aldosterone biosynthesis by dispersed rabbit adreno-capsular cells.  Biochem Bioph Res Co. 1989;  160 628-632
  • 32 Zeng Z, Naruse M, Guan B, Naruse K, Sun M, Zang M, Demura H, Shi Y. Endothelin stimulates aldosterone secretion in vitro from normal adrenocortical tissue, but not adenoma tissue, in primary aldosteronism.  J Clin Endocrinol Metab. 1992;  74 874-878
  • 33 Hu CW, Webb RL, Jeng AY. Synergistic stimulation of aldosterone production in human adrenocortical carcinoma NCI-H295R cells by endothelin-1 and angiotensin II.  J Cardiovasc Pharmacol. 2004;  44 (S 01) S289-S292
  • 34 Vierhapper H, Nowotny P, Waldhäusl W. Effect of endothelin-1 in man: impact on basal and adrenocorticotropinstimulated concentrations of aldosterone.  J Clin Endocrinol Metab. 1995;  80 948-951
  • 35 Morello F, Schiavone D, Mengozzi G, Bertello C, Liew CC, Bisbocci D, Mulatero P, Veglio F. Adrenal endothelin-1 levels are not associated with aldosterone secretion in primary aldosteronism.  Eur J Endocrinol. 2009;  160 453-458
  • 36 Päth G, Bornstein SR, Ehrhart-Bornstein M, Scherbaum WA. Interleukin-6 and the interleukin-6 receptor in the human adrenal gland: expression and effects on steroidogenesis.  J Clin Endocrinol Metab. 1997;  82 2343-2349
  • 37 Reincke M, Beuschlein F, Bidlingmaier M, Funder JW, Bornstein SR. Progress in primary aldosteronism.  Horm Metab Res. 2010;  42 371-373
  • 38 Gomez-Sanchez CE, Rossi GP, Fallo F, Mannelli M. Progress in primary aldosteronism: present challenges and perspectives.  Horm Metab Res. 2010;  42 374-381
  • 39 Mazzuco TL, Grunenwald S, Lampron A, Bourdeau I, Lacroix A. Aberrant hormone receptors in primary aldosteronism.  Horm Metab Res. 2010;  42 416-423

Correspondence

H. S. Willenberg

Department of Endocrinology, Diabetes and Rheumatology

University Hospital Düsseldorf

Moorenstraße 5

40225 Düsseldorf

Germany

Phone: +49/211/811 7810

Fax: +49/211/811 7860

Email: Holger.Willenberg@uni-duesseldorf.de

    >