Melanocortin 2 Receptor-Associated Protein (MRAP) and MRAP2 in Human Adrenocortical Tissues: Regulation of Expression and Association with ACTH Responsiveness

Hans Hofland, Patric Delhanty, J van Steenbergen, Leo Hofland, Peter van Koetsveld, Francien Nederveen, W.W. de Herder, R.A. Feelders, Frank Jong

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Context: ACTH stimulates adrenocortical steroid production through the melanocortin 2 receptor (MC2R). MC2R trafficking and signaling are dependent on the MC2R accessory protein (MRAP). The MRAP homolog MRAP2 also transports the MC2R to the cell surface but might prevent activation. Objective: The objective of the investigation was to study the regulatory pathways of MRAP and MRAP2 and their contributions to ACTH responsiveness in human adrenal tissues. Design and Setting: MRAP, MRAP2, and MC2R expression levels were studied in 32 human adrenocortical samples. Regulation of these mRNAs was investigated in 43 primary adrenal cultures, stimulated with ACTH, forskolin, angiotensin II (AngII), phorbol-12-myristate-13-acetate (PMA), or dexamethasone. The induction of cortisol, cAMP, and ACTH-responsive genes after treatment with ACTH was related to MRAP, MRAP2, and MC2R expression levels. Results: MRAP and MRAP2 levels were lower in adrenocortical carcinomas (ACC) than in other adrenal tissues (P < 0.001). Patient ACTH and cortisol levels were associated with adrenal levels of MRAP and MC2R in adrenal hyperplasia samples (P < 0.05) but not in tumors. ACTH induced the expression of MRAP 11 +/- 2.1-fold and MC2R 20 +/- 3.8-fold in all adrenal tissue types (mean +/- SEM, both P < 0.0001), whereas AngII augmented these mRNAs 4.0 +/- 1.2-fold and 12.6 +/- 3.2-fold (P < 0.0001) in all Conclusion: MRAP and MC2R expression is induced by ACTH and AngII, which would facilitate cell surface receptor availability. Physiological expression levels of MRAP, MRAP2, and MC2R were not limiting for ACTH sensitivity. (J Clin Endocrinol Metab 97: E747-E754, 2012)
Original languageUndefined/Unknown
Pages (from-to)E747-E754
JournalJournal of Clinical Endocrinology and Metabolism
Issue number5
Publication statusPublished - 2012

Research programs

  • EMC MM-01-39-01
  • EMC MM-01-39-04
  • EMC MM-03-24-01

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