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Bento-Lopes, L.; Cabaço, L.C.; Charneca, J.; Neto, M.V.; Seabra, M.C.; Barral, D.C. Melanin Transfer Models. Encyclopedia. Available online: https://encyclopedia.pub/entry/47221 (accessed on 20 December 2024).
Bento-Lopes L, Cabaço LC, Charneca J, Neto MV, Seabra MC, Barral DC. Melanin Transfer Models. Encyclopedia. Available at: https://encyclopedia.pub/entry/47221. Accessed December 20, 2024.
Bento-Lopes, Liliana, Luís C. Cabaço, João Charneca, Matilde V. Neto, Miguel C. Seabra, Duarte C. Barral. "Melanin Transfer Models" Encyclopedia, https://encyclopedia.pub/entry/47221 (accessed December 20, 2024).
Bento-Lopes, L., Cabaço, L.C., Charneca, J., Neto, M.V., Seabra, M.C., & Barral, D.C. (2023, July 25). Melanin Transfer Models. In Encyclopedia. https://encyclopedia.pub/entry/47221
Bento-Lopes, Liliana, et al. "Melanin Transfer Models." Encyclopedia. Web. 25 July, 2023.
Melanin Transfer Models
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This entry is adapted from the peer-reviewed paper 10.3390/ijms241411289

Skin pigmentation ensures efficient photoprotection and relies on the pigment melanin, which is produced by epidermal melanocytes and transferred to surrounding keratinocytes. While the molecular mechanisms of melanin synthesis and transport in melanocytes are now well characterized, much less is known about melanin transfer and processing within keratinocytes.

melanin melanocyte keratinocyte melanosome melanocore

1. Introduction

The skin is the largest organ of the body and plays fundamental roles in water balance, regulation of body temperature, and protection against foreign agents and ultraviolet radiation (UVr) [1]. The upper layer of the skin — the epidermis — is mainly comprised of keratinocytes, which account for >80% of the cells in this layer. Keratinocytes stratify into five different strata according to their differentiation status: stratum basale, stratum spinosum, stratum granulosum, stratum lucidum (only visible in thick skin), and stratum corneum [2][3]. The epidermis also contains melanocytes, which are specialized cells derived from the neural crest during embryonic development [4]. Melanocytes are dispersed throughout the stratum basale and can extend dendrites to contact up to 40 keratinocytes, forming “epidermal-melanin units” (Figure 1A) [5][6]. The function of melanocytes is to synthesize the pigment melanin, subsequently transferring it to keratinocytes [7]. There are two types of melanin: black/brown eumelanin and yellow/red pheomelanin [8][9]. These are synthesized in melanocytes within melanosomes, which are lysosome-related organelles (LROs), as they are endosomal-derived, contain lysosomal markers, and are acidic in the early stages of their biogenesis [10]. Melanosomes display four distinct stages of maturation: In stages I and II, they are non-pigmented, initially resembling multivesicular endosomes. While pheomelanosomes maintain a spherical shape, eumelanosomes acquire an elliptic shape due to internal fibril nucleation of the premelanosomal protein (PMEL) [10]. Melanogenic enzymes required for eumelanin synthesis, including tyrosinase and tyrosinase-related proteins (TYRP1/2), are recruited to stage III melanosomes, and melanin starts to progressively deposit onto PMEL fibrils until melanosomes achieve full pigmentation (stage IV) [10][11]. Mature melanosomes accumulate at melanocyte dendrites and are then transferred to keratinocytes. After being internalized by keratinocytes, melanin is processed, i.e., trafficked, before accumulating in the supranuclear area, where it exerts its function of protecting the DNA of these cells from UVr [12]. In light skins, melanin is present in clusters, whereas dark skins predominantly contain single melanin granules that are usually larger, even though melanin-containing organelles display a similar size in light and dark skins (Figure 1B) [13][14][15][16][17]. Thus, skin pigmentation results from several processes that involve melanin synthesis in melanocytes, transfer from melanocytes to keratinocytes, and processing within keratinocytes. The molecular machinery involved in melanin synthesis and transport within melanocytes is now well characterized, but the mechanisms of melanin transfer remain controversial and poorly characterized. Moreover, only a few studies have addressed how melanin processing occurs within keratinocytes, and much remains to be uncovered.
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Figure 1. Melanin distribution throughout the epidermis and organization within keratinocytes from distinct phototypes. (A) Melanin dispersion in the epidermis is achieved through the formation of epidermal-melanin units. The accumulation of melanin is higher in the basal layers, regardless of the skin phototype (represented by the numbered circles and labeled from I — lower/lighter phototype — to VI — higher/darker phototype). However, in lower phototypes (lighter skins), less melanin is concentrated in the basal layer, whereas in higher phototypes (darker skins), higher levels can be found in the basal layer, and melanin is also present in the immediate suprabasal layers. (B) Melanin organizes differently within keratinocytes derived from different phototypes. In lower phototypes, melanin is mainly stored in clusters of several melanin granules within a single membrane organelle, while higher phototypes prominently accumulate single granules in single membrane organelles.

2. Melanin Transfer Models

Melanin must be transferred to keratinocytes to exert its photoprotective function in these cells. The process by which melanin transfer occurs has been a controversial topic since as far back as the 1960s, when melanin was first observed being transferred from a melanocyte to an epithelial cell (keratinocyte) [18]. As many as four models have been proposed to explain how melanin is transferred from melanocytes to keratinocytes, even though some could be variations of the same: (I) Cytophagocytosis of melanocyte dendrite tips, containing melanosomes, by keratinocytes; (II) Membrane fusion between keratinocytes and melanocytes and direct transfer of melanosomes; (III) Shedding of melanosome-laden globules by melanocytes and subsequent phagocytosis by keratinocytes; and (IV) Exocytosis of the melanin core by melanocytes, followed by phagocytosis by keratinocytes (Figure 2). These are subsequently summarized:
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Figure 2. Melanin transfer from melanocytes to keratinocytes. Four different models have been proposed to explain the mechanism(s) of melanin transfer from melanocytes (dark-colored) to keratinocytes (light-colored), including the cytophagocytosis of melanocyte dendrites by keratinocytes; the direct fusion of melanocyte and keratinocyte membranes; the shedding of melanosome-laden globules by melanocytes; and the coupled exocytosis/phagocytosis of the melanin core. Despite the evidence published using different models, recent studies using human and mouse cell lines, as well as more complex models such as reconstructed human skins/epidermises and skin biopsies, have supported the transfer of melanin in globules or as melanocores.
  • Cytophagocytosis of melanocyte dendrites by keratinocytes.
This transfer mode was first proposed after observations made by electron microscopy (EM) of melanocyte dendrite tips within keratinocytes in vitro [19]. The process can be divided into four steps: Firstly, a melanocyte dendrite tip comes into contact with the keratinocyte plasma membrane and is subsequently engulfed by it; secondly, the melanocyte dendrite tip is pinched off, leading to the formation of a cytoplasmic vesicle filled with melanosomes; and thirdly, the compartment where melanin resides, which is theoretically limited by three membranes of different origins — the innermost one corresponding to the membrane of the melanosome and the plasma membranes of the melanocyte and the keratinocyte — fuses with the lysosome to form a phagolysosome. This leads to the degradation of the luminal membranes [20]. Lastly, the phagolysosome fragments into smaller vesicles containing aggregates or single melanin granules dispersed in the cytoplasm [21].
  • Fusion of melanocyte and keratinocyte membranes.
This model postulates that the plasma membranes of the melanocyte and keratinocyte fuse, allowing the formation of a conduit (e.g., filopodia or nanotubes) between the cytoplasm of the neighboring cells, through which melanosomes are transported [22]. As in the cytophagocytosis model, keratinocytes receive membrane-bound melanosomes. However, melanin within keratinocytes was shown to be devoid of melanosome markers [13][23]. A possible explanation for this discrepancy is that the melanosome membrane is degraded inside keratinocytes by the endolysosomal system. It should be noted that this model and the cytophagocytosis one could represent variations of the same. Indeed, a filopodia-cytophagocytosis model was proposed, in which melanocytes extend filopodia that bind to the keratinocyte plasma membrane and are then pulled and subsequently phagocytosed by the keratinocyte [24][25].
  • Shedding of melanosome-laden globules.
This model proposes that the blebbing of the melanocyte membrane leads to the formation and release of globules (1–3 µm in size) filled with melanosomes, which are then phagocytosed by keratinocytes [26][27]. Recently, other studies showed that globules filled with melanosomes are secreted from primary human melanocyte dendrites to the cell culture medium [28]. These melanosome-laden globules, when isolated from the medium and incubated with primary human keratinocytes, are internalized and processed in a similar manner as postulated by the cytophagocytosis model [29]. Indeed, according to this model, upon internalization, melanin is surrounded by three membranes. After processing, single membrane vesicles containing melanin are dispersed inside keratinocytes [29].
  • Coupled exocytosis/phagocytosis of the melanin core.
This transfer model predicts that melanosomes fuse with the melanocyte plasma membrane, leading to the exocytosis of the naked melanin core, termed melanocore, to the extracellular space and its subsequent internalization by keratinocytes. Consequently, melanocores become surrounded by a single membrane derived from the keratinocyte plasma membrane upon internalization. The first evidence supporting this model came with the observation of extracellular melanin in human hair and skin, which was hypothesized to be internalized by keratinocytes in aggregates or individual granules [30].
The different models are supported by evidence obtained in various experimental systems, namely primary cells, cell lines, and tissue explants from different species, including mice, guinea pigs, chickens, frogs, and humans. In co-cultures of melanocytes and keratinocytes isolated from black guinea pig ears, evidence for the cytophagocytosis transfer model was reported [19]. In frog skin cells and tissues, melanin transfer was described as occurring through shed melanin-laden globules or exo-/phagocytosis of melanosomes, as extracellular melanin was found to be membrane-bound [27]. In chicken embryonic skin, melanin was proposed to be transferred via shed globules [31]. In mice, melanin transfer occurs in the hair follicles, and evidence for the models of exo-/phagocytosis and shed globules has been described [32]. Regarding the different systems used, most studies were performed with cultured melanocytes, either alone or in co-culture with keratinocytes. However, in the skin epidermis, melanin transfer occurs between melanocytes and keratinocytes arranged in epidermal-melanin units. Therefore, models that reproduce this arrangement should be favored. Additionally, the use of melanoma cell lines for the study of the molecular mechanisms of pigment transfer should be performed with caution, as they can show alterations in melanin production, processing, and secretion [33]. Importantly, the model of exo-/phagocytosis is the one that collected more supporting evidence from the analysis of human skin sections and reconstructed human skin/epidermis in vitro models [23][34]. The shed globules is the other model that has been more explored. Furthermore, the four models can be essentially divided into the one that postulates the transfer of naked melanin (melanocore) and the ones that predict the transfer of membrane-bound melanosomes. It should be noted that it cannot be excluded that several mechanisms of melanin transfer co-exist, even in the same organism, as adaptations to different physiological or pathological conditions. To solve these long-lasting questions, a better understanding at the cellular and molecular levels of the pathways and regulators of melanin exocytosis from melanocytes and internalization by keratinocytes is essential.

References

  1. Grice, E.A.; Segre, J.A. The skin microbiome. Nat. Rev. Microbiol. 2011, 9, 244–253.
  2. Solanas, G.; Benitah, S.A. Regenerating the skin: A task for the heterogeneous stem cell pool and surrounding niche. Nat. Rev. Mol. Cell Biol. 2013, 14, 737–748.
  3. Kolarsick, P.A.J.; Kolarsick, M.A.; Goodwin, C. Anatomy and Physiology of the Skin. J. Dermatol. Nurses Assoc. 2011, 3, 203–213.
  4. Plonka, P.M.; Passeron, T.; Brenner, M.; Tobin, D.J.; Shibahara, S.; Thomas, A.; Slominski, A.; Kadekaro, A.L.; Hershkovitz, D.; Peters, E.; et al. What are melanocytes really doing all day long…? Exp. Dermatol. 2009, 18, 799–819.
  5. Cox, N.H. Fitzpatrick’s Dermatology in General Medicine. Br. J. Dermatol. 2004, 150, 794.
  6. Lin, J.Y.; Fisher, D.E. Melanocyte biology and skin pigmentation. Nature 2007, 445, 843–850.
  7. Wasmeier, C.; Hume, A.N.; Bolasco, G.; Seabra, M.C. Melanosomes at a glance. J. Cell Sci. 2008, 121, 3995–3999.
  8. Ito, S.; Wakamatsu, K. Chemistry of mixed melanogenesis–pivotal roles of dopaquinone. Photochem. Photobiol. 2008, 84, 582–592.
  9. Ito, S.; Wakamatsu, K. Human hair melanins: What we have learned and have not learned from mouse coat color pigmentation. Pigment Cell Melanoma Res. 2011, 24, 63–74.
  10. Raposo, G.; Tenza, D.; Murphy, D.M.; Berson, J.F.; Marks, M.S. Distinct protein sorting and localization to premelanosomes, melanosomes, and lysosomes in pigmented melanocytic cells. J. Cell Biol. 2001, 152, 809–823.
  11. Raposo, G.; Marks, M.S. The dark side of lysosome-related organelles: Specialization of the endocytic pathway for melanosome biogenesis. Traffic 2002, 3, 237–248.
  12. Byers, H.R.; Maheshwary, S.; Amodeo, D.M.; Dykstra, S.G. Role of Cytoplasmic Dynein in Perinuclear Aggregation of Phagocytosed Melanosomes and Supranuclear Melanin Cap Formation in Human Keratinocytes. J. Investig. Dermatol. 2003, 121, 813–820.
  13. Hurbain, I.; Romao, M.; Sextius, P.; Bourreau, E.; Marchal, C.; Bernerd, F.; Duval, C.; Raposo, G. Melanosome Distribution in Keratinocytes in Different Skin Types: Melanosome Clusters Are Not Degradative Organelles. J. Investig. Dermatol. 2018, 138, 647–656.
  14. SzabÓ, G.; Gerald, A.B.; Pathak, M.A.; Fitzpatrick, T.B Racial differences in the fate of melanosomes in human epidermis. Nature 1969, 222, 1081–1082.
  15. Minwalla, L.; Zhao, Y.; Boissy, R.E.; le Poole, I.C.; Wickett, R.R. Keratinocytes Play a Role in Regulating Distribution Patterns of Recipient Melanosomes In Vitro. J. Investig. Dermatol. 2001, 117(2), 341-347.
  16. Yoshida, Y.; Hachiya, A.; Sriwiriyanont, P.; Ohuchi, A.; Kitahara, T.; Takema, Y.; Visscher, M.O.; Boissy, R.E. Functional analysis of keratinocytes in skin color using a human skin substitute model composed of cells derived from different skin pigmentation types. FASEB J. 2007, 21, 2829–2839.
  17. Thong, H.Y.; Jee, S.H.; Sun, C.C.; Boissy, R.E. The patterns of melanosome distribution in keratinocytes of human skin as one determining factor of skin colour. Br. J. Dermatol. 2003, 149, 498–505.
  18. Cruickshank, C.N.; Harcourt, S.A. Pigment donation in vitro. J. Investig. Dermatol. 1964, 42, 183–184.
  19. Okazaki, K.; Uzuka, M.; Morikawa, F.; Toda, K.; Seiji, M. Transfer mechanism of melanosomes in epidermal cell culture. J. Investig. Dermatol. 1976, 67, 541–547.
  20. Wolff, K. Melanocyte-keratinocyte interactions in vivo: The fate of melanosomes. Yale J. Biol. Med. 1973, 46, 384.
  21. Yamamoto, O.; Bhawan, J. Three modes of melanosome transfers in Caucasian facial skin: Hypothesis based on an ultrastructural study. Pigment Cell Res. 1994, 7, 158–169.
  22. Scott, G.; Leopardi, S.; Printup, S.; Madden, B.C. Filopodia are conduits for melanosome transfer to keratinocytes. J. Cell Sci. 2002, 115, 1441–1451.
  23. Tarafder, A.K.; Bolasco, G.; Correia, M.S.; Pereira, F.J.; Iannone, L.; Hume, A.N.; Kirkpatrick, N.; Picardo, M.; Torrisi, M.R.; Rodrigues, I.P.; et al. Rab11b mediates melanin transfer between donor melanocytes and acceptor keratinocytes via coupled exo/endocytosis. J. Investig. Dermatol. 2014, 134, 1056–1066.
  24. Singh, S.K.; Kurfurst, R.; Nizard, C.; Schnebert, S.; Perrier, E.; Tobin, D.J. Melanin transfer in human skin cells is mediated by filopodia—A model for homotypic and heterotypic lysosome-related organelle transfer. FASEB J. 2010, 24, 3756–3769.
  25. Singh, S.K.; Baker, R.; Sikkink, S.K.; Nizard, C.; Schnebert, S.; Kurfurst, R.; Tobin, D.J. E-cadherin mediates ultraviolet radiation- and calcium-induced melanin transfer in human skin cells. Exp. Dermatol. 2017, 26, 1125–1133.
  26. Cerdan, D.; Redziniak, G.; Bourgeois, C.A.; Monsigny, M.; Kieda, C. C32 human melanoma cell endogenous lectins: Characterization and implication in vesicle-mediated melanin transfer to keratinocytes. Exp. Cell Res. 1992, 203, 164–173.
  27. Aspengren, S.; Hedberg, D.; Wallin, M. Studies of pigment transfer between Xenopus laevis melanophores and fibroblasts in vitro and in vivo. Pigment Cell Res. 2006, 19, 136–145.
  28. Ando, H.; Niki, Y.; Yoshida, M.; Ito, M.; Akiyama, K.; Kim, J.H.; Yoon, T.J.; Matsui, M.S.; Yarosh, D.B.; Ichihashi, M. Involvement of pigment globules containing multiple melanosomes in the transfer of melanosomes from melanocytes to keratinocytes. Cell. Logist. 2011, 1, 12–20.
  29. Ando, H.; Niki, Y.; Ito, M.; Akiyama, K.; Matsui, M.S.; Yarosh, D.B.; Ichihashi, M. Melanosomes are transferred from melanocytes to keratinocytes through the processes of packaging, release, uptake, and dispersion. J. Investig. Dermatol. 2012, 132, 1222–1229.
  30. Swift, J.A. Transfer of melanin granules from melanocytes to the cortical cells of human hair. Nature 1964, 203, 976–977.
  31. Tadokoro, R.; Murai, H.; Sakai, K.I.; Okui, T.; Yokota, Y.; Takahashi, Y. Melanosome transfer to keratinocyte in the chicken embryonic skin is mediated by vesicle release associated with Rho-regulated membrane blebbing. Sci. Rep. 2016, 6, 38277.
  32. Wu, X.; Hammer, J.A. Melanosome transfer: It is best to give and receive. Curr. Opin. Cell Biol. 2014, 29, 1–7.
  33. Cabaço, L.C.; Tomás, A.; Pojo, M.; Barral, D.C. The dark side of melanin secretion in cutaneous melanoma aggressiveness. Front. Oncol. 2022, 12, 887366.
  34. Hall, M.J.; Lopes-Ventura, S.; Neto, M.V.; Charneca, J.; Zoio, P.; Seabra, M.C.; Oliva, A.; Barral, D.C. Reconstructed human pigmented skin/epidermis models achieve epidermal pigmentation through melanocore transfer. Pigment Cell Melanoma Res. 2022, 35, 425–435.
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Subjects: Cell Biology
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
Liliana Bento-Lopes
,
Luís C. Cabaço
,
João Charneca
,
Matilde V. Neto
,
Miguel C. Seabra
,
Duarte C. Barral
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Update Date: 02 Aug 2023
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