Light or Dark Pigmentation of Engineered Skin Substitutes Containing Melanocytes Protects Against Ultraviolet Light-Induced DNA Damage In Vivo. 2020

Dorothy M Supp, and Jennifer M Hahn, and Christopher M Lloyd, and Kelly A Combs, and Viki B Swope, and Zalfa Abdel-Malek, and Steven T Boyce
Research Department, Shriners Hospitals for Children - Cincinnati, Ohio.

Engineered skin substitutes (ESS) containing autologous fibroblasts and keratinocytes provide stable wound closure in patients with large, full-thickness burns, but are limited by hypopigmentation due to absence of added melanocytes. DNA damage caused by ultraviolet radiation (UV) increases risk for skin cancer development. In human skin, melanocytes provide pigmentation that protects skin from UV-induced DNA damage. This study investigated whether inclusion of human melanocytes (hM) affects the response of ESS to UV in vivo. Specifically, pigmentation and formation of cyclobutane pyrimidine dimers (CPDs), the most prevalent UV-induced DNA photoproduct, were analyzed. Three groups of ESS were prepared with fibroblasts and keratinocytes, ± melanocytes, and grafted orthotopically to immunodeficient mice: ESS without melanocytes (ESS-hM), ESS with light skin-derived (Caucasian) melanocytes (ESS+hM-L), and ESS with dark skin-derived (African-American) melanocytes (ESS+hM-D). Pigmentation of ESS+hM-L and ESS+hM-D increased significantly after grafting; pigmentation levels were significantly different among groups. Mean melanocyte densities in ESS+hM-L and ESS+hM-D were similar to each other and to densities in normal human skin. After 8 weeks in vivo, grafts were irradiated with 135 mJ/cm2 UV; non-UV-treated mice served as controls. UV modestly increased pigmentation in the ESS+hM groups. UV significantly increased CPD levels in ESS-hM, and levels in ESS-hM were significantly greater than in ESS+hM-L or ESS+hM-D. The results demonstrate that light or dark melanocytes in ESS decreased UV-induced DNA damage. Therefore, melanocytes in ESS play a photoprotective role. Protection against UV-induced DNA damage is expected to reduce skin cancer risk in patients grafted with ESS containing autologous melanocytes.

UI MeSH Term Description Entries
D008544 Melanocytes Mammalian pigment cells that produce MELANINS, pigments found mainly in the EPIDERMIS, but also in the eyes and the hair, by a process called melanogenesis. Coloration can be altered by the number of melanocytes or the amount of pigment produced and stored in the organelles called MELANOSOMES. The large non-mammalian melanin-containing cells are called MELANOPHORES. Melanocyte
D004249 DNA Damage Injuries to DNA that introduce deviations from its normal, intact structure and which may, if left unrepaired, result in a MUTATION or a block of DNA REPLICATION. These deviations may be caused by physical or chemical agents and occur by natural or unnatural, introduced circumstances. They include the introduction of illegitimate bases during replication or by deamination or other modification of bases; the loss of a base from the DNA backbone leaving an abasic site; single-strand breaks; double strand breaks; and intrastrand (PYRIMIDINE DIMERS) or interstrand crosslinking. Damage can often be repaired (DNA REPAIR). If the damage is extensive, it can induce APOPTOSIS. DNA Injury,DNA Lesion,DNA Lesions,Genotoxic Stress,Stress, Genotoxic,Injury, DNA,DNA Injuries
D005347 Fibroblasts Connective tissue cells which secrete an extracellular matrix rich in collagen and other macromolecules. Fibroblast
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D012880 Skin Pigmentation Coloration of the skin. Skin Color,Skin Tone,Color, Skin,Colors, Skin,Pigmentation, Skin,Pigmentations, Skin,Skin Colors,Skin Pigmentations,Skin Tones,Tone, Skin,Tones, Skin
D014466 Ultraviolet Rays That portion of the electromagnetic spectrum immediately below the visible range and extending into the x-ray frequencies. The longer wavelengths (near-UV or biotic or vital rays) are necessary for the endogenous synthesis of vitamin D and are also called antirachitic rays; the shorter, ionizing wavelengths (far-UV or abiotic or extravital rays) are viricidal, bactericidal, mutagenic, and carcinogenic and are used as disinfectants. Actinic Rays,Black Light, Ultraviolet,UV Light,UV Radiation,Ultra-Violet Rays,Ultraviolet Light,Ultraviolet Radiation,Actinic Ray,Light, UV,Light, Ultraviolet,Radiation, UV,Radiation, Ultraviolet,Ray, Actinic,Ray, Ultra-Violet,Ray, Ultraviolet,Ultra Violet Rays,Ultra-Violet Ray,Ultraviolet Black Light,Ultraviolet Black Lights,Ultraviolet Radiations,Ultraviolet Ray
D015603 Keratinocytes Epidermal cells which synthesize keratin and undergo characteristic changes as they move upward from the basal layers of the epidermis to the cornified (horny) layer of the skin. Successive stages of differentiation of the keratinocytes forming the epidermal layers are basal cell, spinous or prickle cell, and the granular cell. Keratinocyte
D017768 Skin, Artificial Synthetic material used for the treatment of burns and other conditions involving large-scale loss of skin. It often consists of an outer (epidermal) layer of silicone and an inner (dermal) layer of collagen and chondroitin 6-sulfate. The dermal layer elicits new growth and vascular invasion and the outer layer is later removed and replaced by a graft. Artificial Skin,Skin Substitutes,Artificial Skins,Skin Substitute,Skins, Artificial,Substitute, Skin,Substitutes, Skin
D051379 Mice The common name for the genus Mus. Mice, House,Mus,Mus musculus,Mice, Laboratory,Mouse,Mouse, House,Mouse, Laboratory,Mouse, Swiss,Mus domesticus,Mus musculus domesticus,Swiss Mice,House Mice,House Mouse,Laboratory Mice,Laboratory Mouse,Mice, Swiss,Swiss Mouse,domesticus, Mus musculus

Related Publications

Dorothy M Supp, and Jennifer M Hahn, and Christopher M Lloyd, and Kelly A Combs, and Viki B Swope, and Zalfa Abdel-Malek, and Steven T Boyce
May 2013, The British journal of dermatology,
Dorothy M Supp, and Jennifer M Hahn, and Christopher M Lloyd, and Kelly A Combs, and Viki B Swope, and Zalfa Abdel-Malek, and Steven T Boyce
January 2021, The Journal of investigative dermatology,
Dorothy M Supp, and Jennifer M Hahn, and Christopher M Lloyd, and Kelly A Combs, and Viki B Swope, and Zalfa Abdel-Malek, and Steven T Boyce
July 2002, Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology,
Dorothy M Supp, and Jennifer M Hahn, and Christopher M Lloyd, and Kelly A Combs, and Viki B Swope, and Zalfa Abdel-Malek, and Steven T Boyce
November 2015, Molecules (Basel, Switzerland),
Dorothy M Supp, and Jennifer M Hahn, and Christopher M Lloyd, and Kelly A Combs, and Viki B Swope, and Zalfa Abdel-Malek, and Steven T Boyce
January 2017, Pigment cell & melanoma research,
Dorothy M Supp, and Jennifer M Hahn, and Christopher M Lloyd, and Kelly A Combs, and Viki B Swope, and Zalfa Abdel-Malek, and Steven T Boyce
October 2007, Clinical cancer research : an official journal of the American Association for Cancer Research,
Dorothy M Supp, and Jennifer M Hahn, and Christopher M Lloyd, and Kelly A Combs, and Viki B Swope, and Zalfa Abdel-Malek, and Steven T Boyce
December 1970, The Journal of investigative dermatology,
Dorothy M Supp, and Jennifer M Hahn, and Christopher M Lloyd, and Kelly A Combs, and Viki B Swope, and Zalfa Abdel-Malek, and Steven T Boyce
September 2003, The Journal of investigative dermatology,
Dorothy M Supp, and Jennifer M Hahn, and Christopher M Lloyd, and Kelly A Combs, and Viki B Swope, and Zalfa Abdel-Malek, and Steven T Boyce
January 2007, Skin pharmacology and physiology,
Dorothy M Supp, and Jennifer M Hahn, and Christopher M Lloyd, and Kelly A Combs, and Viki B Swope, and Zalfa Abdel-Malek, and Steven T Boyce
December 2023, Biochemical and biophysical research communications,
Copied contents to your clipboard!