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Assessment of Melanogenesis in a Pigmented Human Tissue-Cultured Skin Equivalent

BACKGROUND: Organotypic tissue-cultured skin equivalents are used for a broad range of applications either as possible substitute for animal tests or for transplantation in patient-centered care. AIMS: In this study, we implemented melanocytes in a tissue-cultured full-thickness skin equivalent, con...

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Autores principales: Zöller, Nadja Nicole, Hofmann, Matthias, Butting, Manuel, Hrgovic, Igor, Bereiter-Hahn, Jürgen, Bernd, August, Kaufmann, Roland, Kippenberger, Stefan, Valesky, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6440179/
https://www.ncbi.nlm.nih.gov/pubmed/30983601
http://dx.doi.org/10.4103/ijd.IJD_410_17
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author Zöller, Nadja Nicole
Hofmann, Matthias
Butting, Manuel
Hrgovic, Igor
Bereiter-Hahn, Jürgen
Bernd, August
Kaufmann, Roland
Kippenberger, Stefan
Valesky, Eva
author_facet Zöller, Nadja Nicole
Hofmann, Matthias
Butting, Manuel
Hrgovic, Igor
Bereiter-Hahn, Jürgen
Bernd, August
Kaufmann, Roland
Kippenberger, Stefan
Valesky, Eva
author_sort Zöller, Nadja Nicole
collection PubMed
description BACKGROUND: Organotypic tissue-cultured skin equivalents are used for a broad range of applications either as possible substitute for animal tests or for transplantation in patient-centered care. AIMS: In this study, we implemented melanocytes in a tissue-cultured full-thickness skin equivalent, consisting of epidermis and dermis. The versatility of this skin-like model with respect to pigmentation and morphological criteria was tested. MATERIALS AND METHODS: Pigmented skin equivalents were morphologically characterized, and melanogenesis was evaluated after treatment with kojic acid – a tyrosinase inhibitor and forskolin – a well-known activator of the cyclic adenosine 3,5-monophosphate pathway. Pigmentation was measured either by determination of the extinction at 400 nm after melanin extraction with KOH correlated to a melanin standard curve or by reflectance colorimetric analysis, monitoring reflectance of 660 nm and 880 nm emitting diodes. RESULTS: The morphological analysis revealed characteristic epidermal stratification with melanocytes located at the basal layer. Stimulation with forskolin increased the pigmentation, whereas treatment with kojic acid caused bleaching. CONCLUSION: The present study demonstrates that the herein-introduced organotypic tissue-cultured skin equivalent is comparable to the normal human skin and its versatility in tests regarding skin pigmentation. Therefore, this model might help understand diseases with dysfunctional pigmentation such as melasma, vitiligo, and postinflammatory hyperpigmentation.
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spelling pubmed-64401792019-04-12 Assessment of Melanogenesis in a Pigmented Human Tissue-Cultured Skin Equivalent Zöller, Nadja Nicole Hofmann, Matthias Butting, Manuel Hrgovic, Igor Bereiter-Hahn, Jürgen Bernd, August Kaufmann, Roland Kippenberger, Stefan Valesky, Eva Indian J Dermatol Basic Research BACKGROUND: Organotypic tissue-cultured skin equivalents are used for a broad range of applications either as possible substitute for animal tests or for transplantation in patient-centered care. AIMS: In this study, we implemented melanocytes in a tissue-cultured full-thickness skin equivalent, consisting of epidermis and dermis. The versatility of this skin-like model with respect to pigmentation and morphological criteria was tested. MATERIALS AND METHODS: Pigmented skin equivalents were morphologically characterized, and melanogenesis was evaluated after treatment with kojic acid – a tyrosinase inhibitor and forskolin – a well-known activator of the cyclic adenosine 3,5-monophosphate pathway. Pigmentation was measured either by determination of the extinction at 400 nm after melanin extraction with KOH correlated to a melanin standard curve or by reflectance colorimetric analysis, monitoring reflectance of 660 nm and 880 nm emitting diodes. RESULTS: The morphological analysis revealed characteristic epidermal stratification with melanocytes located at the basal layer. Stimulation with forskolin increased the pigmentation, whereas treatment with kojic acid caused bleaching. CONCLUSION: The present study demonstrates that the herein-introduced organotypic tissue-cultured skin equivalent is comparable to the normal human skin and its versatility in tests regarding skin pigmentation. Therefore, this model might help understand diseases with dysfunctional pigmentation such as melasma, vitiligo, and postinflammatory hyperpigmentation. Wolters Kluwer - Medknow 2019 /pmc/articles/PMC6440179/ /pubmed/30983601 http://dx.doi.org/10.4103/ijd.IJD_410_17 Text en Copyright: © 2019 Indian Journal of Dermatology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Basic Research
Zöller, Nadja Nicole
Hofmann, Matthias
Butting, Manuel
Hrgovic, Igor
Bereiter-Hahn, Jürgen
Bernd, August
Kaufmann, Roland
Kippenberger, Stefan
Valesky, Eva
Assessment of Melanogenesis in a Pigmented Human Tissue-Cultured Skin Equivalent
title Assessment of Melanogenesis in a Pigmented Human Tissue-Cultured Skin Equivalent
title_full Assessment of Melanogenesis in a Pigmented Human Tissue-Cultured Skin Equivalent
title_fullStr Assessment of Melanogenesis in a Pigmented Human Tissue-Cultured Skin Equivalent
title_full_unstemmed Assessment of Melanogenesis in a Pigmented Human Tissue-Cultured Skin Equivalent
title_short Assessment of Melanogenesis in a Pigmented Human Tissue-Cultured Skin Equivalent
title_sort assessment of melanogenesis in a pigmented human tissue-cultured skin equivalent
topic Basic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6440179/
https://www.ncbi.nlm.nih.gov/pubmed/30983601
http://dx.doi.org/10.4103/ijd.IJD_410_17
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