Visiting Research Fellow. Present Address: Fujita Health University, School of Health Sciences, Toyoake, Aichi, 470-11, Japan.
Characterisation of ACTH Peptides in Human Skin and Their Activation of the Melanocortin-1 Receptor
Article first published online: 28 JUL 2006
Pigment Cell Research
Volume 10, Issue 5, pages 288–297, October 1997
How to Cite
WAKAMATSU, K., GRAHAM, A., COOK, D. and THODY, A. J. (1997), Characterisation of ACTH Peptides in Human Skin and Their Activation of the Melanocortin-1 Receptor. Pigment Cell Research, 10: 288–297. doi: 10.1111/j.1600-0749.1997.tb00688.x
Presented in part at the European Society for Dermatological Research Meeting, Amsterdam, September 1996 and at the XVI International Pigment Cell Conference, Anaheim, October 1996.
- Issue published online: 28 JUL 2006
- Article first published online: 28 JUL 2006
- Received February 9, 1997; accepted June 6, 1997.
- Melanocortin-1 receptor;
α-Melanocyte-stimulating hormone (α-MSH) is a proopiomelanocortin (POMC)-derived peptide, which is produced in the pituitary and at other sites including the skin. It has numerous effects and in the skin has a pigmentary action through the activation of the melanocortin-1 (MC-1) receptor, which is expressed by melanocytes. Recent evidence suggests that the related POMC peptides such as adrenocorticotrophin (ACTH), which is the precursor of α-MSH, is also an agonist at the MC-1 receptor. By using immunocytochemistry, we confirmed the presence of α-MSH in human skin where staining was evident in keratinocytes and especially strong in melanocytes and possibly Langerhans cells. ACTH was also present and tended to show the strongest reaction in differentiated keratinocytes. Immunostaining was also observed for the prohormone convertases, PC1 and PC2, which are involved in the formation of ACTH and its cleavage to α-MSH, respectively. The amounts of immunoreactive ACTH exceeded those of α-MSH. Using HPLC we identified for the first time the presence of ACTH1-39, ACTH1-17, ACTH1-10, acetylated ACTH1-10, α-MSH, and desacetyl α-MSH in epidermis and in cultured keratinocytes. The ability of these peptides to activate the human MC-1 receptor was examined in HEK 293 cells that had been transfected with the receptor. All peptides increased adenylate cyclase in these cells with the following order of potency: ACTH1-17 > α-MSH > ACTH1-39 > desacetyl α-MSH > acetylated ACTH1-10 > ACTH1-10. ACTH1-17 also increased the dendricity and melanin content of cultured human melanocytes indicating that the peptide was able to activate MC-1 receptors when present in their normal location. However, as found with α-MSH, not all cultures were responsive and, as we have previously suggested, we suspect that this was the result of changes at the MC-1 receptor. Nevertheless, it would appear that ACTH peptides can serve as natural ligands of the MC-1 receptor on human melanocytes and their presence in the skin suggests that, together with α-MSH, they may have a role in the regulation of human melanocytes.