Intracellular signaling mechanisms of the melanocortin receptors: current state of the art
Open accessAbstract
The melanocortin system is composed by the agonists adrenocorticotropic hormone and α, β and γ-melanocyte-stimulating hormone, and two naturally occurring antagonists, agouti and agouti-related protein. These ligands act by interaction with a family of five melanocortin receptors (MCRs), assisted by MCRs accessory proteins (MRAPs). MCRs stimulation activates different signaling pathways that mediate a diverse array of physiological processes, including pigmentation, energy metabolism, inflammation and exocrine secretion. This review focuses on the regulatory mechanisms of MCRs signaling, highlighting the differences among the five receptors. MCRs signal through G-dependent and independent mechanisms and their functional coupling to agonists at the cell surface is regulated by interacting proteins, namely MRAPs and β-arrestins. The knowledge of the distinct modulation pattern of MCRs signaling and function may be helpful for the future design of novel drugs able to combine specificity, safety and effectiveness in the course of their therapeutic use.
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Melanocortin receptors, which mediate the neuroprotective effect of α-MSH, activate CREB.
“Moreover, melanocortin receptors, which mediate the neuroprotective effect of α-MSH, activate CREB [42].”
From Brain Protein Expression Profile Confirms the Protective Effect of the ACTH(4–7)PGP Peptide (Semax) in a Rat Model of Cerebral Ischemia–Reperfusion (2021) · cites this paper as [42]
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Adrenocorticotropin insensitivity syndromes
Clark, A. J. L., & Weber, A. (1998) · Endocrine Reviews · doi:10.1210/edrv.19.6.0351 · Cited by 234 · see citing works
Chung, T. T., Webb, T. R., Chan, L. F., Cooray, S. N., Metherell, L. A., King, P. J., Chapple, J. P., & Clark, A. J. L. (2008) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2008-1744 · Cited by 82 · see citing works
Winnay, J. N., & Hammer, G. D. (2006) · Molecular Endocrinology · doi:10.1210/me.2005-0215 · Cited by 74 · see citing works
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Sudarkina, O. Y., Filippenkov, I. B., Stavchansky, V. V., Denisova, A. E., Yuzhakov, V. V., Sevan’kaeva, L. E., Valieva, L. V., Remizova, J. A., Dmitrieva, V. G., Gubsky, L. V., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22126179 · Cited by 15 · see citing works
“Moreover, melanocortin receptors, which mediate the neuroprotective effect of α-MSH, activate CREB [42].”
Background
- Authors
- Rodrigues, A. R., Almeida, H., & Gouveia, A. M.
- Affiliations
- Universidade do Porto (PT)
- Corresponding author
- Gouveia, Alexandra M.
- Venue
- Cellular and Molecular Life Sciences
- Published
- 2014-12-12
- Volume
- 72
- Issue
- 7
- Pages
- 1331-1345
- ISSN
- 1420-682X (ISSN-L)
- 1420-9071
- PMC
- PMC11113477
- OpenAlex
- W2011491214
- Cited by
- 64
- References
- 3
- Citations by year
- 2026: 4 · 2025: 2 · 2024: 3 · 2023: 9 · 2022: 10 · 2021: 8 · 2020: 4 · 2019: 5 · 2018: 7 · 2017: 6 · 2016: 4 · 2015: 2
- FWCI
- 0.38
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Cellular and Molecular Life Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT) (submittedVersion)
- Funders
- Fundação para a Ciência e a Tecnologia
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
- Keywords
- melanocortin receptors, intracellular signaling, melanocortin system, ACTH, melanocyte-stimulating hormone, agouti, agouti-related protein, beta-arrestin, G protein-coupled receptor signaling, pigmentation, energy metabolism, inflammation, drug design
- MeSH terms
- Cell Physiological Phenomena, Humans, Ligands, Models, Biological, Protein Binding, Signal Transduction, GTP-Binding Proteins, Protein Isoforms, Intracellular Space, Receptors, Melanocortin
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