Reconstructed human pigmented skin/epidermis models achieve epidermal pigmentation through melanocore transfer

• Published in: Pigment cell and melanoma research Vol. 35; no. 4; pp. 425 - 435
• Main Authors: Hall, Michael J., Lopes‐Ventura, Sara, Neto, Matilde V., Charneca, João, Zoio, Patricia, Seabra, Miguel C., Oliva, Abel, Barral, Duarte C.
• Format: Journal Article
• Language: English
• Published: England Wiley Subscription Services, Inc 01.07.2022
• Subjects: 3D models; Aging; Animal models; Biopsy; Crosstalk; Deoxyribonucleic acid; Dispersion; DNA; DNA damage; Epidermis; Exocytosis; Fibroblasts; Histology; Immunohistochemistry; Keratinocytes; Melanin; melanin transfer; Melanocytes; Phagocytosis; Pigmentation; Skin cancer; Skin pigmentation; Transmission electron microscopy; Ultraviolet radiation; pigmentation; melanocytes; keratinocytes; 3D models; melanin transfer
• ISSN: 1755-1471; 1755-148X
• DOI: 10.1111/pcmr.13039

The skin acts as a barrier to environmental insults and provides many vital functions. One of these is to shield DNA from harmful ultraviolet radiation, which is achieved by skin pigmentation arising as melanin is produced and dispersed within the epidermal layer. This is a crucial defence against DNA damage, photo‐ageing and skin cancer. The mechanisms and regulation of melanogenesis and melanin transfer involve extensive crosstalk between melanocytes and keratinocytes in the epidermis, as well as fibroblasts in the dermal layer. Although the predominant mechanism of melanin transfer continues to be debated and several plausible models have been proposed, we and others previously provided evidence for a coupled exo/phagocytosis model. Herein, we performed histology and immunohistochemistry analyses and demonstrated that a newly developed full‐thickness three‐dimensional reconstructed human pigmented skin model and an epidermis‐only model exhibit dispersed pigment throughout keratinocytes in the epidermis. Transmission electron microscopy revealed melanocores between melanocytes and keratinocytes, suggesting that melanin is transferred through coupled exocytosis/phagocytosis of the melanosome core, or melanocore, similar to our previous observations in human skin biopsies. We, therefore, present evidence that our in vitro models of pigmented human skin show epidermal pigmentation comparable to human skin. These findings have a high value for studies of skin pigmentation mechanisms and pigmentary disorders, whilst reducing the reliance on animal models and human skin biopsies.