Melanin

Melanin
One possible structure of Eumelanin
One possible structure of Eumelanin
Material typeHeterogeneous biopolymer
Micrograph of Melanin pigment (light refracting granular material—center of image) in a pigmented melanoma.
Micrograph of the epidermis, with melanin labeled at left.

Melanin (/ˈmɛlənɪn/ ; from Ancient Greek μέλας (mélas) 'black, dark') is a family of biomolecules organized as oligomers or polymers, which among other functions provide the pigments of many organisms.[1] Melanin pigments are produced in a specialized group of cells known as melanocytes.

There are five basic types of melanin: eumelanin, pheomelanin, neuromelanin, allomelanin and pyomelanin.[2] Melanin is produced through a multistage chemical process known as melanogenesis, where the oxidation of the amino acid tyrosine is followed by polymerization. Pheomelanin is a cysteinated form containing polybenzothiazine portions that are largely responsible for the red or yellow tint given to some skin or hair colors. Neuromelanin is found in the brain. Research has been undertaken to investigate its efficacy in treating neurodegenerative disorders such as Parkinson's.[3] Allomelanin and pyomelanin are two types of nitrogen-free melanin.

The phenotypic color variation observed in the epidermis and hair of mammals is primarily determined by the levels of eumelanin and pheomelanin in the examined tissue. In an average human individual, eumelanin is more abundant in tissues requiring photoprotection, such as the epidermis and the retinal pigment epithelium.[4] In healthy subjects, epidermal melanin is correlated with UV exposure, while retinal melanin has been found to correlate with age, with levels diminishing 2.5-fold between the first and ninth decades of life,[5] which has been attributed to oxidative degradation mediated by reactive oxygen species generated via lipofuscin-dependent pathways.[6] In the absence of albinism or hyperpigmentation, the human epidermis contains approximately 74% eumelanin and 26% pheomelanin, largely irrespective of skin tone, with eumelanin content ranging between 71.8–78.9%, and pheomelanin varying between 21.1–28.2%.[7] Total melanin content in the epidermis ranges from around 0 μg/mg in albino epidermal tissue[8] to >10 μg/mg in darker tissue.[9]

In the human skin, melanogenesis is initiated by exposure to UV radiation, causing the skin to darken. Eumelanin is an effective absorbent of light; the pigment is able to dissipate over 99.9% of absorbed UV radiation.[10] Because of this property, eumelanin is thought to protect skin cells from UVA and UVB radiation damage, reducing the risk of folate depletion and dermal degradation. Exposure to UV radiation is associated with increased risk of malignant melanoma, a cancer of melanocytes (melanin cells). Studies have shown a lower incidence for skin cancer in individuals with more concentrated melanin, i.e. darker skin tone.[11]

  1. ^ Casadevall A (2018). "Melanin triggers antifungal defences". Nature. 555 (7696): 319–320. Bibcode:2018Natur.555..319C. doi:10.1038/d41586-018-02370-x. ISSN 0028-0836. PMID 29542711. S2CID 3832753.
  2. ^ Cao W, Zhou X, McCallum NC, Hu Z, Ni QZ, Kapoor U, et al. (9 February 2021). "Unraveling the Structure and Function of Melanin through Synthesis". Journal of the American Chemical Society. 143 (7): 2622–2637. doi:10.1021/jacs.0c12322. hdl:1854/LU-8699336. ISSN 0002-7863. PMID 33560127. S2CID 231872855. Archived from the original on 30 August 2024. Retrieved 13 February 2021.
  3. ^ Haining RL, Achat-Mendes C (March 2017). "Neuromelanin, one of the most overlooked molecules in modern medicine, is not a spectator". Neural Regeneration Research. 12 (3): 372–375. doi:10.4103/1673-5374.202928. PMC 5399705. PMID 28469642.
  4. ^ Istrate M, Vlaicu B, Poenaru M, Hasbei-Popa M, Salavat M, Iliescu D (April 2020). "Photoprotection role of melanin in the human retinal pigment epithelium. Imaging techniques for retinal melanin". Romanian Journal of Opthalmology. 64 (2): 100–104. doi:10.22336/rjo.2020.20. PMC 7339703. PMID 32685774.
  5. ^ Sarna T, Burke J, Korytowski W, Rózanowska M, Skumatz C, Zareba A, et al. (January 2003). "Loss of melanin from human RPE with aging: possible role of melanin photooxidation". Experimental Eye Research. 76 (1): 89–98. doi:10.1016/s0014-4835(02)00247-6. PMID 12589778. Retrieved 26 October 2024.
  6. ^ Dontsov A, Yakovleva M, Vasin A, Gulin A, Aybush A, Nadtochenko V, et al. (August 2023). "Understanding the Mechanism of Light-Induced Age-Related Decrease in Melanin Concentration in Retinal Pigment Epithelium Cells". International Journal of Molecular Sciences. 24 (17): 13099. doi:10.3390/ijms241713099. PMC 10487480. PMID 37685907.
  7. ^ Del Bino S, Ito S, Juliette S, Nakanishi Y, Bastien P, Wakamatsu K, et al. (18 August 2015). "Chemical analysis of constitutive pigmentation of human epidermis reveals constant eumelanin to pheomelanin ratio". Pigment Cell & Melanoma Research. 28 (6): 707–17. doi:10.1111/pcmr.12410. PMID 26285058. Retrieved 26 October 2024.
  8. ^ Marçon C, Maia M (30 September 2019). "Albinism: epidemiology, genetics, cutaneous characterization, psychosocial factors☆☆☆". Anais Brasileiros de Dermatologia. 94 (5): 503–520. doi:10.1016/j.abd.2019.09.023. PMC 6857599. PMID 31777350.
  9. ^ Del Bino S, Ito S, Juliette S, Nakanishi Y, Bastien P, Wakamatsu K, et al. (18 August 2015). "Chemical analysis of constitutive pigmentation of human epidermis reveals constant eumelanin to pheomelanin ratio". Pigment Cell & Melanoma Research. 28 (6): 707–17. doi:10.1111/pcmr.12410. PMID 26285058. Retrieved 26 October 2024.
  10. ^ Meredith P, Riesz J (2004). "Radiative relaxation quantum yields for synthetic eumelanin". Photochemistry and Photobiology. 79 (2): 211–6. arXiv:cond-mat/0312277. doi:10.1111/j.1751-1097.2004.tb00012.x. PMID 15068035. S2CID 222101966.
  11. ^ Brenner M, Hearing VJ (2008). "The protective role of melanin against UV damage in human skin". Photochemistry and Photobiology. 84 (3): 539–49. doi:10.1111/j.1751-1097.2007.00226.x. PMC 2671032. PMID 18435612.

Melanin

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