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Adipose tissue-derived extracellular fraction characterization: biological and clinical considerations in regenerative medicine

BACKGROUND: Adipose tissue-derived stem cells are considered to be a promising source in the field of cell therapy and regenerative medicine. In addition to direct cell replacement using adipose tissue or purified stem cells, intercellular molecule exchange by the adipose tissue complex, a vast arra...

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Autores principales: Bellei, Barbara, Migliano, Emilia, Tedesco, Marinella, Caputo, Silvia, Papaccio, Federica, Lopez, Gianluca, Picardo, Mauro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085647/
https://www.ncbi.nlm.nih.gov/pubmed/30092820
http://dx.doi.org/10.1186/s13287-018-0956-4
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author Bellei, Barbara
Migliano, Emilia
Tedesco, Marinella
Caputo, Silvia
Papaccio, Federica
Lopez, Gianluca
Picardo, Mauro
author_facet Bellei, Barbara
Migliano, Emilia
Tedesco, Marinella
Caputo, Silvia
Papaccio, Federica
Lopez, Gianluca
Picardo, Mauro
author_sort Bellei, Barbara
collection PubMed
description BACKGROUND: Adipose tissue-derived stem cells are considered to be a promising source in the field of cell therapy and regenerative medicine. In addition to direct cell replacement using adipose tissue or purified stem cells, intercellular molecule exchange by the adipose tissue complex, a vast array of bioactive secretory factors, demonstrated beneficial effects by reducing tissue damage and stimulation of endogenous repair. However, for therapeutic purposes, the use of secretome derivatives, such as full conditioned media or purified exosomes generated in vitro, may present considerable disadvantages for cell manufacturing, storage, product safety, and their potential as a ready-to-go therapeutic product. METHODS: In this study, the effect of a liquid fraction of lipoaspirates isolated intraoperatively from 28 healthy donors was evaluated for their protective effect against oxidative stress and senescence, proliferation, and migration in vitro on normal human melanocytes, keratinocytes, and fibroblasts. Immunoenzymatic quantification of several growth factors and important signal molecules was used to define the biological profile of physiological adipose tissue secretome. RESULTS: Adipose tissue extracellular fraction (AT-Ex), isolated from lipoaspirate, exhibited significant potential for skin repair. AT-Ex augmented dermal and epidermal cell proliferation in a dose-dependent manner without promoting cancer cell growth. Moreover, migration of dermal fibroblasts, an important phenomenon implicated in endogenous repair, was enhanced by AT-Ex treatment. AT-Ex has a positive impact on oxidative stress damage when cells are exposed to extrinsic hostile factors and prevent a fibroblast senescence phenotype including paracrine functions associated with skin aging. CONCLUSIONS: Collectively, our findings propose natural systems carrying the physiological balance of in-vivo produced secretome that could improve cutaneous wound healing and tissue repair. This approach, representing an innovative perspective and therapeutic strategy in regenerative medicine, could also be combined with autologous stem cell grafts to treat chronic nonhealing wounds, stable vitiligo, severe burns, and post-oncological scarring. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-018-0956-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-60856472018-08-16 Adipose tissue-derived extracellular fraction characterization: biological and clinical considerations in regenerative medicine Bellei, Barbara Migliano, Emilia Tedesco, Marinella Caputo, Silvia Papaccio, Federica Lopez, Gianluca Picardo, Mauro Stem Cell Res Ther Research BACKGROUND: Adipose tissue-derived stem cells are considered to be a promising source in the field of cell therapy and regenerative medicine. In addition to direct cell replacement using adipose tissue or purified stem cells, intercellular molecule exchange by the adipose tissue complex, a vast array of bioactive secretory factors, demonstrated beneficial effects by reducing tissue damage and stimulation of endogenous repair. However, for therapeutic purposes, the use of secretome derivatives, such as full conditioned media or purified exosomes generated in vitro, may present considerable disadvantages for cell manufacturing, storage, product safety, and their potential as a ready-to-go therapeutic product. METHODS: In this study, the effect of a liquid fraction of lipoaspirates isolated intraoperatively from 28 healthy donors was evaluated for their protective effect against oxidative stress and senescence, proliferation, and migration in vitro on normal human melanocytes, keratinocytes, and fibroblasts. Immunoenzymatic quantification of several growth factors and important signal molecules was used to define the biological profile of physiological adipose tissue secretome. RESULTS: Adipose tissue extracellular fraction (AT-Ex), isolated from lipoaspirate, exhibited significant potential for skin repair. AT-Ex augmented dermal and epidermal cell proliferation in a dose-dependent manner without promoting cancer cell growth. Moreover, migration of dermal fibroblasts, an important phenomenon implicated in endogenous repair, was enhanced by AT-Ex treatment. AT-Ex has a positive impact on oxidative stress damage when cells are exposed to extrinsic hostile factors and prevent a fibroblast senescence phenotype including paracrine functions associated with skin aging. CONCLUSIONS: Collectively, our findings propose natural systems carrying the physiological balance of in-vivo produced secretome that could improve cutaneous wound healing and tissue repair. This approach, representing an innovative perspective and therapeutic strategy in regenerative medicine, could also be combined with autologous stem cell grafts to treat chronic nonhealing wounds, stable vitiligo, severe burns, and post-oncological scarring. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-018-0956-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-09 /pmc/articles/PMC6085647/ /pubmed/30092820 http://dx.doi.org/10.1186/s13287-018-0956-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Bellei, Barbara
Migliano, Emilia
Tedesco, Marinella
Caputo, Silvia
Papaccio, Federica
Lopez, Gianluca
Picardo, Mauro
Adipose tissue-derived extracellular fraction characterization: biological and clinical considerations in regenerative medicine
title Adipose tissue-derived extracellular fraction characterization: biological and clinical considerations in regenerative medicine
title_full Adipose tissue-derived extracellular fraction characterization: biological and clinical considerations in regenerative medicine
title_fullStr Adipose tissue-derived extracellular fraction characterization: biological and clinical considerations in regenerative medicine
title_full_unstemmed Adipose tissue-derived extracellular fraction characterization: biological and clinical considerations in regenerative medicine
title_short Adipose tissue-derived extracellular fraction characterization: biological and clinical considerations in regenerative medicine
title_sort adipose tissue-derived extracellular fraction characterization: biological and clinical considerations in regenerative medicine
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6085647/
https://www.ncbi.nlm.nih.gov/pubmed/30092820
http://dx.doi.org/10.1186/s13287-018-0956-4
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