Cited by 98melanin and skin pigmentationMelanoma and MAPK PathwaysCutaneous Melanoma Detection and Management

Melanosome Distribution in Keratinocytes in Different Skin Types: Melanosome Clusters Are Not Degradative Organelles

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Hurbain, Ilse, Romao, Maryse, Sextius, Peggy, Bourreau, Emilie, Marchal, Céline, Bernerd, Françoise, Duval, Christine, Raposo, Graça·2018·Journal of Investigative Dermatology

Abstract

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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Crossref · 10.1016/j.jid.2017.09.039

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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)

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  • Melanin-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 measured
  • Melanin 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 measured
  • MKSs 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 measured
  • Melanocores 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 ].”

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References 34 · Cited by 98

Research works printed but not linked: 1

  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
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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