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The Multifaceted Melanocortin Receptors
The 5 known melanocortin receptors (MCs) have established physiological roles. With the exception of MC(2), these receptors can behave unpredictably, and since they are more widely expressed than their established roles would suggest, it is likely that they have other poorly characterized functions....
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214563/ https://www.ncbi.nlm.nih.gov/pubmed/35700124 http://dx.doi.org/10.1210/endocr/bqac083 |
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author | Laiho, Linda Murray, Joanne Fiona |
author_facet | Laiho, Linda Murray, Joanne Fiona |
author_sort | Laiho, Linda |
collection | PubMed |
description | The 5 known melanocortin receptors (MCs) have established physiological roles. With the exception of MC(2), these receptors can behave unpredictably, and since they are more widely expressed than their established roles would suggest, it is likely that they have other poorly characterized functions. The aim of this review is to discuss some of the less well-explored aspects of the 4 enigmatic members of this receptor family (MC(1,3-5)) and describe how these are multifaceted G protein–coupled receptors (GPCRs). These receptors appear to be promiscuous in that they bind several endogenous agonists (products of the proopiomelanocortin [POMC] gene) and antagonists but with inconsistent relative affinities and effects. We propose that this is a result of posttranslational modifications that determine receptor localization within nanodomains. Within each nanodomain there will be a variety of proteins, including ion channels, modifying proteins, and other GPCRs, that can interact with the MCs to alter the availability of receptor at the cell surface as well as the intracellular signaling resulting from receptor activation. Different combinations of interacting proteins and MCs may therefore give rise to the complex and inconsistent functional profiles reported for the MCs. For further progress in understanding this family, improved characterization of tissue-specific functions is required. Current evidence for interactions of these receptors with a range of partners, resulting in modulation of cell signaling, suggests that each should be studied within the full context of their interacting partners. The role of physiological status in determining this context also remains to be characterized. |
format | Online Article Text |
id | pubmed-9214563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-92145632022-06-23 The Multifaceted Melanocortin Receptors Laiho, Linda Murray, Joanne Fiona Endocrinology Mini-Review The 5 known melanocortin receptors (MCs) have established physiological roles. With the exception of MC(2), these receptors can behave unpredictably, and since they are more widely expressed than their established roles would suggest, it is likely that they have other poorly characterized functions. The aim of this review is to discuss some of the less well-explored aspects of the 4 enigmatic members of this receptor family (MC(1,3-5)) and describe how these are multifaceted G protein–coupled receptors (GPCRs). These receptors appear to be promiscuous in that they bind several endogenous agonists (products of the proopiomelanocortin [POMC] gene) and antagonists but with inconsistent relative affinities and effects. We propose that this is a result of posttranslational modifications that determine receptor localization within nanodomains. Within each nanodomain there will be a variety of proteins, including ion channels, modifying proteins, and other GPCRs, that can interact with the MCs to alter the availability of receptor at the cell surface as well as the intracellular signaling resulting from receptor activation. Different combinations of interacting proteins and MCs may therefore give rise to the complex and inconsistent functional profiles reported for the MCs. For further progress in understanding this family, improved characterization of tissue-specific functions is required. Current evidence for interactions of these receptors with a range of partners, resulting in modulation of cell signaling, suggests that each should be studied within the full context of their interacting partners. The role of physiological status in determining this context also remains to be characterized. Oxford University Press 2022-06-14 /pmc/articles/PMC9214563/ /pubmed/35700124 http://dx.doi.org/10.1210/endocr/bqac083 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Mini-Review Laiho, Linda Murray, Joanne Fiona The Multifaceted Melanocortin Receptors |
title | The Multifaceted Melanocortin Receptors |
title_full | The Multifaceted Melanocortin Receptors |
title_fullStr | The Multifaceted Melanocortin Receptors |
title_full_unstemmed | The Multifaceted Melanocortin Receptors |
title_short | The Multifaceted Melanocortin Receptors |
title_sort | multifaceted melanocortin receptors |
topic | Mini-Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214563/ https://www.ncbi.nlm.nih.gov/pubmed/35700124 http://dx.doi.org/10.1210/endocr/bqac083 |
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