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Dehydrated human amnion/chorion membrane regulates stem cell activity in vitro

Human‐derived placental tissues have been shown in randomized clinical trials to be effective for healing chronic wounds, and have also demonstrated the ability to recruit stem cells to the wound site in vitro and in vivo. In this study, PURION(®) Processed dehydrated human amnion/chorion membrane a...

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Autores principales: Massee, Michelle, Chinn, Kathryn, Lei, Jennifer, Lim, Jeremy J., Young, Conan S., Koob, Thomas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054843/
https://www.ncbi.nlm.nih.gov/pubmed/26175122
http://dx.doi.org/10.1002/jbm.b.33478
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author Massee, Michelle
Chinn, Kathryn
Lei, Jennifer
Lim, Jeremy J.
Young, Conan S.
Koob, Thomas J.
author_facet Massee, Michelle
Chinn, Kathryn
Lei, Jennifer
Lim, Jeremy J.
Young, Conan S.
Koob, Thomas J.
author_sort Massee, Michelle
collection PubMed
description Human‐derived placental tissues have been shown in randomized clinical trials to be effective for healing chronic wounds, and have also demonstrated the ability to recruit stem cells to the wound site in vitro and in vivo. In this study, PURION(®) Processed dehydrated human amnion/chorion membrane allografts (dHACM, EpiFix(®), MiMedx Group, Marietta, GA) were evaluated for their ability to alter stem cell activity in vitro. Human bone marrow mesenchymal stem cells (BM‐MSCs), adipose derived stem cells (ADSCs), and hematopoietic stem cells (HSCs) were treated with soluble extracts of dHACM tissue, and were evaluated for cellular proliferation, migration, and cytokine secretion. Stem cells were analyzed for cell number by DNA assay after 24 h, closure of an acellular zone using microscopy over 3 days, and soluble cytokine production in the medium of treated stem cells was analyzed after 3 days using a multiplex ELISA array. Treatment with soluble extracts of dHACM tissue stimulated BM‐MSCs, ADSCs, and HSCs to proliferate with a significant increase in cell number after 24 h. dHACM treatment accelerated closure of an acellular zone by ADSCs and BM‐MSCs after 3 days, compared to basal medium. BM‐MSCs, ADSCs, and HSCs also modulated endogenous production of a number of various soluble signals, including regulators of inflammation, mitogenesis, and wound healing. dHACM treatment promoted increased proliferation and migration of ADSCs, BM‐MSCs, and HSCs, along with modulation of secreted proteins from those cells. Therefore, dHACM may impact wound healing by amplifying host stem cell populations and modulating their responses in treated wound tissues. © 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 104B: 1495–1503, 2016.
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spelling pubmed-50548432016-10-19 Dehydrated human amnion/chorion membrane regulates stem cell activity in vitro Massee, Michelle Chinn, Kathryn Lei, Jennifer Lim, Jeremy J. Young, Conan S. Koob, Thomas J. J Biomed Mater Res B Appl Biomater Clinical Device‐Related Article Human‐derived placental tissues have been shown in randomized clinical trials to be effective for healing chronic wounds, and have also demonstrated the ability to recruit stem cells to the wound site in vitro and in vivo. In this study, PURION(®) Processed dehydrated human amnion/chorion membrane allografts (dHACM, EpiFix(®), MiMedx Group, Marietta, GA) were evaluated for their ability to alter stem cell activity in vitro. Human bone marrow mesenchymal stem cells (BM‐MSCs), adipose derived stem cells (ADSCs), and hematopoietic stem cells (HSCs) were treated with soluble extracts of dHACM tissue, and were evaluated for cellular proliferation, migration, and cytokine secretion. Stem cells were analyzed for cell number by DNA assay after 24 h, closure of an acellular zone using microscopy over 3 days, and soluble cytokine production in the medium of treated stem cells was analyzed after 3 days using a multiplex ELISA array. Treatment with soluble extracts of dHACM tissue stimulated BM‐MSCs, ADSCs, and HSCs to proliferate with a significant increase in cell number after 24 h. dHACM treatment accelerated closure of an acellular zone by ADSCs and BM‐MSCs after 3 days, compared to basal medium. BM‐MSCs, ADSCs, and HSCs also modulated endogenous production of a number of various soluble signals, including regulators of inflammation, mitogenesis, and wound healing. dHACM treatment promoted increased proliferation and migration of ADSCs, BM‐MSCs, and HSCs, along with modulation of secreted proteins from those cells. Therefore, dHACM may impact wound healing by amplifying host stem cell populations and modulating their responses in treated wound tissues. © 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 104B: 1495–1503, 2016. John Wiley and Sons Inc. 2015-07-14 2016-10 /pmc/articles/PMC5054843/ /pubmed/26175122 http://dx.doi.org/10.1002/jbm.b.33478 Text en © 2015 The Authors. Journal of Biomedical Materials Research Part A Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Clinical Device‐Related Article
Massee, Michelle
Chinn, Kathryn
Lei, Jennifer
Lim, Jeremy J.
Young, Conan S.
Koob, Thomas J.
Dehydrated human amnion/chorion membrane regulates stem cell activity in vitro
title Dehydrated human amnion/chorion membrane regulates stem cell activity in vitro
title_full Dehydrated human amnion/chorion membrane regulates stem cell activity in vitro
title_fullStr Dehydrated human amnion/chorion membrane regulates stem cell activity in vitro
title_full_unstemmed Dehydrated human amnion/chorion membrane regulates stem cell activity in vitro
title_short Dehydrated human amnion/chorion membrane regulates stem cell activity in vitro
title_sort dehydrated human amnion/chorion membrane regulates stem cell activity in vitro
topic Clinical Device‐Related Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5054843/
https://www.ncbi.nlm.nih.gov/pubmed/26175122
http://dx.doi.org/10.1002/jbm.b.33478
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