The Proopiomelanocortin System

POMC (31,000 MW) is localized to the pituitary, brain, skin, and other peripheral sites. The particular enzyme profile present within a cell dictates the nature of the hormonal ligand (melanocortin) synthesized and secreted: melanotropic peptides (α‐MSH β‐lipotropin, λ‐MSH), corticotropin (ACTH), se...

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Bibliographic Details
Published in:Annals of the New York Academy of Sciences 1999-10, Vol.885 (1), p.1-21
Main Authors: HADLEY, MAC E., HASKELL-LUEVANO, CARRIE
Format: Article
Language:English
Subjects:
Adrenocorticotropic Hormone - physiology
Amino Acid Sequence
Animals
Annexins - physiology
Endorphins - physiology
Homeostasis
Humans
Melanocyte-Stimulating Hormones - physiology
Molecular Sequence Data
Pro-Opiomelanocortin - chemistry
Pro-Opiomelanocortin - physiology
Protein Conformation
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Summary:POMC (31,000 MW) is localized to the pituitary, brain, skin, and other peripheral sites. The particular enzyme profile present within a cell dictates the nature of the hormonal ligand (melanocortin) synthesized and secreted: melanotropic peptides (α‐MSH β‐lipotropin, λ‐MSH), corticotropin (ACTH), several endorphins (e.g., met‐enkephalin). These POMC‐derived peptides mediate their actions through typical seven‐spanning membrane receptors (MCRs; MCR1, 2, 3, 4, and 5). A specific melanocortin acting on a specific MCR regulates a particular biological response; for example, α‐MSH on MCR1 increases melanogenesis within melanocytes, ACTH on MCR2 increases cortisol production within adrenal zona fasciculata cells. Within the brain melanocortins regulate satiety (MCR4) and erectile activity (MCR?). MCRs have been localized by melanocortin macromolecular probes, for example, fluorescent to human epidermal melanocytes and also to keratinocytes, suggesting that systemic melanocortins or localized POMC products might regulate these integumental cellular elements in synchrony to enhance skin pigmentation and/or immunological responses. Superpotent, prolonged acting melanotropic peptides have been synthesized and their application in clinical medicine has been demonstrated. MCR antagonists have been used to discover and further delineate other roles of melanocortin ligands. For example, melanocortin‐induced satiety can be antagonized by a melanocortin antagonist. Defects in melanocortin ligand biosynthesis, secretion, and melanocortin receptor function can lead to a diverse number of pathological states.
ISSN:0077-8923
1749-6632
DOI:10.1111/j.1749-6632.1999.tb08662.x