Melanosome Distribution in Keratinocytes in Different Skin Types: Melanosome Clusters Are Not Degradative Organelles
Open accessAbstract
The melanosome pattern was characterized systematically in keratinocytes in situ in highly, moderately, and lightly pigmented human skin, classified according to the individual typological angle, a colorimetric measure of skin color phenotype. Electron microscopy of skin samples showed qualitatively and quantitatively that in highly pigmented skin, although melanosomes are mostly isolated and distributed throughout the entire epidermis, clusters are also observed in the basal layer. In moderately and lightly pigmented skin, melanosomes are concentrated in the first layer of the epidermis, isolated-but for most of them, grouped as clusters of melanocores delimited by a single membrane. Electron tomography resolving intracellular three-dimensional organization of organelles showed that clustered melanocores depict contacts with other cellular compartments, such as endoplasmic reticulum and mitochondria. Additionally, immunogold labelling showed that clusters of melanocores do not correspond to autophagosomes or melanophagosomes but that they present, similarly to melanosomes in melanocytes, features of nonacidic, nondegradative organelles. Overall, these observations suggest that melanocore clusters do not correspond to autophagic organelles but represent reservoirs or protective structures for melanosome integrity and function. These results open avenues for understanding the basis of skin pigmentation in different skin color phenotypes.
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Melanin within keratinocytes is devoid of melanosome markers.
“melanin within keratinocytes was shown by us and the group of Graça Raposo to be devoid of melanosome markers [ 18 , 19 ].”
From Melanin's Journey from Melanocytes to Keratinocytes: Uncovering the Molecular Mechanisms of Melanin Transfer and Processing (2023) · cites this paper as [18]
In “Clustered melanocores are not autophagosomes and acidic organelles” (page unavailable), the paper reports that LAMP1 and CD63—identified there as melanosomal/lysosomal membrane proteins—are detected around isolated and clustered melanocores in keratinocytes. Although it describes melanocores as lacking their original melanosomal membrane, it does not say that melanin-containing structures in keratinocytes are devoid of melanosome markers. (LLM, conf=0.89)
Checked by a reasoning model — may be wrong.
Experimental — accuracy not yet measuredMelanin-containing organelles display a similar size in light and dark skins.
“even though melanin-containing organelles display a similar size in light and dark skins [ 18 , 88 , 89 , 90 , 91 ]”
From Melanin's Journey from Melanocytes to Keratinocytes: Uncovering the Molecular Mechanisms of Melanin Transfer and Processing (2023) · cites this paper as [18]
In “Melanosomes are differently distributed in human skin depending on pigmentation level” (page not provided), the paper says clusters of small melanosomes in lightly pigmented skin are comparable in size to large individual melanosomes in highly pigmented skin. But it also reports that isolated melanosomes are significantly smaller in moderately and lightly pigmented skin, so the unqualified claim of similar size overstates the finding. (LLM, conf=0.88)
Experimental — accuracy not yet measuredMelanin accumulates in moderately acidic compartments with low degradative capacity, as shown by low Lysotracker and DAMP accumulation and low DQ-BSA fluorescence, despite the abundance of these organelles within keratinocytes.
“Moreover, we and Graça Raposo’s group showed that melanin accumulates in moderately acidic compartments (presenting low levels of Lysotracker and DAMP [3-(2,4-dinitroanilino)-3′-amino-N-methyldipropylamine] accumulation) with low degradative capacity, as shown by the low levels of dye quenched-bovine serum albumin (DQ-BSA) fluorescence, despite the abundance of these types of organelles within ker”
From Melanin's Journey from Melanocytes to Keratinocytes: Uncovering the Molecular Mechanisms of Melanin Transfer and Processing (2023) · cites this paper as [18]
The section “Clustered melanocores are not autophagosomes and acidic organelles” reports that DAMP was barely detected in transferred melanosomes and clusters and describes the clusters as nondegradative, with a higher pH than lysosomes. It does not report LysoTracker accumulation or DQ-BSA fluorescence, so those specific measurements attributed to this paper are unsupported. (LLM, conf=0.87)
Experimental — accuracy not yet measuredMKSs are likely unique melanin-storage compartments presenting low acidity and degradative capacity but maintaining characteristics of LEs/lysosomes, including membrane markers LAMP1/2 and CD63.
“MKSs are likely unique melanin-storage compartments presenting low acidity and degradative capacity but maintaining characteristics of LEs/lysosomes, including the membrane markers LAMP1/2 and CD63 [ 18 , 27 ]”
From Melanin's Journey from Melanocytes to Keratinocytes: Uncovering the Molecular Mechanisms of Melanin Transfer and Processing (2023) · cites this paper as [18]
In “Clustered melanocores are not autophagosomes and acidic organelles” (page unavailable), the paper reports LAMP1 and CD63 on cluster membranes, little acidity, and no lysosomal hydrolases; it proposes that the clusters may be melanin reservoirs. It does not report LAMP2 on those membranes, so that marker is not supported by this source. (LLM, conf=0.88)
Experimental — accuracy not yet measuredMelanocores are observed in the interstitial space between melanocytes and keratinocytes.
“More recently, we and others provided further evidence supporting this model, in which melanocores were observed in the interstitial space between melanocytes and keratinocytes [ 18 , 19 ].”
From Melanin's Journey from Melanocytes to Keratinocytes: Uncovering the Molecular Mechanisms of Melanin Transfer and Processing (2023) · cites this paper as [18]
In light skins, melanin is present in clusters.
“In light skins, melanin is present in clusters, whereas dark skins predominantly contain single melanin granules that are usually larger”
From Melanin's Journey from Melanocytes to Keratinocytes: Uncovering the Molecular Mechanisms of Melanin Transfer and Processing (2023) · cites this paper as [18]
Experimental — accuracy not yet measuredMelanin is not found in double membrane organelles (autophagosomes) within keratinocytes.
“Notwithstanding these observations, melanin is not found in double membrane organelles, i.e., autophagosomes, within keratinocytes”
From Melanin's Journey from Melanocytes to Keratinocytes: Uncovering the Molecular Mechanisms of Melanin Transfer and Processing (2023) · cites this paper as [18]
Melanin organization within keratinocytes differs between phototypes.
“Importantly, it is well established that melanin organization within keratinocytes differs between phototypes [ 18 , 88 , 89 , 90 , 91 ].”
From Melanin's Journey from Melanocytes to Keratinocytes: Uncovering the Molecular Mechanisms of Melanin Transfer and Processing (2023) · cites this paper as [18]
Melanin-containing compartments lack the classical autophagosomal protein LC3.
“and melanin-containing compartments lack the classical autophagosomal protein LC3 [ 18 , 104 ].”
From Melanin's Journey from Melanocytes to Keratinocytes: Uncovering the Molecular Mechanisms of Melanin Transfer and Processing (2023) · cites this paper as [18]
In dark skins, melanin predominantly consists of single melanin granules that are usually larger.
“In light skins, melanin is present in clusters, whereas dark skins predominantly contain single melanin granules that are usually larger”
From Melanin's Journey from Melanocytes to Keratinocytes: Uncovering the Molecular Mechanisms of Melanin Transfer and Processing (2023) · cites this paper as [18]
Melanin is found in single membrane compartments inside keratinocytes.
“Indeed, melanin is found in single membrane compartments inside keratinocytes, supporting exo-/phagocytosis or the fusion of melanocyte and keratinocyte membrane transfer models [ 17 , 18 , 19 ]”
From Melanin's Journey from Melanocytes to Keratinocytes: Uncovering the Molecular Mechanisms of Melanin Transfer and Processing (2023) · cites this paper as [18]
LAMP1 and CD63 are present in the membrane of single and clustered melanocores, independently of skin phototype.
“Graça Raposo’s group showed that, independently of the skin phototype, the lysosomal-associated membrane protein 1 (LAMP1) and the tetraspanin cell surface antigen 63 (CD63)—markers of late endosomes (LEs)/lysosomes—are present in the membrane of single and clustered melanocores [ 18 ]”
From Melanin's Journey from Melanocytes to Keratinocytes: Uncovering the Molecular Mechanisms of Melanin Transfer and Processing (2023) · cites this paper as [18]
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References 34 · Cited by 98
Research works printed but not linked: 1
- [17]17. Hideya A, Yoko N, Masaki Y, Masaaki I, Kaoru A, Jin-Hwa K, et al. Kerati- nocytes in culture accumulate phagocytosed melanosomes in the peri- nuclear area. Pigment Cell Melanoma Res 2009;23:129e33.
- Authors
- Hurbain, I., Romao, M., Sextius, P., Bourreau, E., Marchal, C., Bernerd, F., Duval, C., & Raposo, G.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- L'Oréal (France) (FR)
- Corresponding author
- Raposo, Graça
- Venue
- Journal of Investigative Dermatology
- Publisher
- Elsevier BV
- Published
- 2018-03
- Volume
- 138
- Issue
- 3
- Pages
- 647-656
- ISSN
- 0022-202X (ISSN-L)
- OpenAlex
- W2765878873
- Cited by
- 98
- References
- 34
- Citations by year
- 2026: 8 · 2025: 21 · 2024: 12 · 2023: 10 · 2022: 8 · 2021: 10 · 2020: 11 · 2019: 9 · 2018: 9
- FWCI
- 4.23
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Journal of Investigative Dermatology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Infrastructures en Biologie Santé et Agronomie
- Agence Nationale de la Recherche (ANR-10–INSB–04, ANR-10-IDEX-0001, ANR-10-IDEX0001-02., ANR-10-IDEX, ANR-10-LBX-0038, ANR10IDEX000102 PSL, ANR-10, IDEX-0001-02)
- Indo-French Centre for the Promotion of Advanced Research
- Labex CelTisPhyBio (ANR-10-IDEX-0001-02 PSL, ANR-10-LBX-0038, ANR-10-IDEX-0001-02)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › melanin and skin pigmentation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Melanoma and MAPK Pathways
- Health Sciences › Medicine › Oncology › Cutaneous Melanoma Detection and Management
- Keywords
- keratinocytes, skin pigmentation, autophagosomes, epidermis, melanosome degradation
- MeSH terms
- Autophagosomes, Adult, Epidermis, Female, Humans, Microscopy, Electron, Skin Pigmentation, Organelles, Keratinocytes, Melanosomes
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