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Conditioned Medium from H(2)O(2)-Preconditioned Human Adipose-Derived Stem Cells Ameliorates UVB-Induced Damage to Human Dermal Fibroblasts

Human skin exposure to ultraviolet B (UVB) radiation can result in acute photodamage through oxidative modifications of cellular components and biomolecules involved in the metabolism of dermal cells. Recently, the therapeutic potential of human adipose-derived stem cells (hASCs) has been investigat...

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Autores principales: Burón, María, Palomares, Teodoro, Garrido-Pascual, Patricia, Herrero de la Parte, Borja, García-Alonso, Ignacio, Alonso-Varona, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9598226/
https://www.ncbi.nlm.nih.gov/pubmed/36290734
http://dx.doi.org/10.3390/antiox11102011
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author Burón, María
Palomares, Teodoro
Garrido-Pascual, Patricia
Herrero de la Parte, Borja
García-Alonso, Ignacio
Alonso-Varona, Ana
author_facet Burón, María
Palomares, Teodoro
Garrido-Pascual, Patricia
Herrero de la Parte, Borja
García-Alonso, Ignacio
Alonso-Varona, Ana
author_sort Burón, María
collection PubMed
description Human skin exposure to ultraviolet B (UVB) radiation can result in acute photodamage through oxidative modifications of cellular components and biomolecules involved in the metabolism of dermal cells. Recently, the therapeutic potential of human adipose-derived stem cells (hASCs) has been investigated as a novel strategy for photoprotection due to their pro-angiogenic properties, protective activity against oxidative stress and paracrine effect on dermal cells. To enhance these therapeutic properties, hASCs can be preconditioned by exposing them to sublethal cellular stressors. In this study, we first analyzed response capacity against UVB-induced oxidative stress in H(2)O(2)-preconditioned hASCs (called HC016 cells); and second, we evaluated the photoprotective effect of HC016-conditioned medium (CM) in an in vitro UVB irradiation model in cultured human foreskin fibroblasts (hFFs). The results demonstrated that HC016 cells have a greater capacity to respond efficiently to UVB-induced oxidative stress, evidenced by higher Nrf2 antioxidant system activity and enhanced viability and migration capacity. Further, HC016-CM treatment increased viability, migratory capacity and collagen type I synthesis in hFFs exposed to UVB radiation, as well as reducing their cytotoxicity, apoptosis, senescence and IL-6 secretion. Collectively, these findings support the view that HC016 cells could protect against UVB-induced photodamage via paracrine mechanisms.
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spelling pubmed-95982262022-10-27 Conditioned Medium from H(2)O(2)-Preconditioned Human Adipose-Derived Stem Cells Ameliorates UVB-Induced Damage to Human Dermal Fibroblasts Burón, María Palomares, Teodoro Garrido-Pascual, Patricia Herrero de la Parte, Borja García-Alonso, Ignacio Alonso-Varona, Ana Antioxidants (Basel) Article Human skin exposure to ultraviolet B (UVB) radiation can result in acute photodamage through oxidative modifications of cellular components and biomolecules involved in the metabolism of dermal cells. Recently, the therapeutic potential of human adipose-derived stem cells (hASCs) has been investigated as a novel strategy for photoprotection due to their pro-angiogenic properties, protective activity against oxidative stress and paracrine effect on dermal cells. To enhance these therapeutic properties, hASCs can be preconditioned by exposing them to sublethal cellular stressors. In this study, we first analyzed response capacity against UVB-induced oxidative stress in H(2)O(2)-preconditioned hASCs (called HC016 cells); and second, we evaluated the photoprotective effect of HC016-conditioned medium (CM) in an in vitro UVB irradiation model in cultured human foreskin fibroblasts (hFFs). The results demonstrated that HC016 cells have a greater capacity to respond efficiently to UVB-induced oxidative stress, evidenced by higher Nrf2 antioxidant system activity and enhanced viability and migration capacity. Further, HC016-CM treatment increased viability, migratory capacity and collagen type I synthesis in hFFs exposed to UVB radiation, as well as reducing their cytotoxicity, apoptosis, senescence and IL-6 secretion. Collectively, these findings support the view that HC016 cells could protect against UVB-induced photodamage via paracrine mechanisms. MDPI 2022-10-11 /pmc/articles/PMC9598226/ /pubmed/36290734 http://dx.doi.org/10.3390/antiox11102011 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Burón, María
Palomares, Teodoro
Garrido-Pascual, Patricia
Herrero de la Parte, Borja
García-Alonso, Ignacio
Alonso-Varona, Ana
Conditioned Medium from H(2)O(2)-Preconditioned Human Adipose-Derived Stem Cells Ameliorates UVB-Induced Damage to Human Dermal Fibroblasts
title Conditioned Medium from H(2)O(2)-Preconditioned Human Adipose-Derived Stem Cells Ameliorates UVB-Induced Damage to Human Dermal Fibroblasts
title_full Conditioned Medium from H(2)O(2)-Preconditioned Human Adipose-Derived Stem Cells Ameliorates UVB-Induced Damage to Human Dermal Fibroblasts
title_fullStr Conditioned Medium from H(2)O(2)-Preconditioned Human Adipose-Derived Stem Cells Ameliorates UVB-Induced Damage to Human Dermal Fibroblasts
title_full_unstemmed Conditioned Medium from H(2)O(2)-Preconditioned Human Adipose-Derived Stem Cells Ameliorates UVB-Induced Damage to Human Dermal Fibroblasts
title_short Conditioned Medium from H(2)O(2)-Preconditioned Human Adipose-Derived Stem Cells Ameliorates UVB-Induced Damage to Human Dermal Fibroblasts
title_sort conditioned medium from h(2)o(2)-preconditioned human adipose-derived stem cells ameliorates uvb-induced damage to human dermal fibroblasts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9598226/
https://www.ncbi.nlm.nih.gov/pubmed/36290734
http://dx.doi.org/10.3390/antiox11102011
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