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Human mesenchymal stem cell sheets in xeno-free media for possible allogenic applications

Cell-based therapies are increasingly focused on allogeneic stem cell sources because of several advantages in eliminating donor variability (e.g., aging and disease pathophysiology) affecting stem cell quality and in cell-banked sourcing of healthy donors to enable “off-the-shelf” products. However...

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Autores principales: Kim, Kyungsook, Bou-Ghannam, Sophia, Thorp, Hallie, Grainger, David W., Okano, Teruo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783458/
https://www.ncbi.nlm.nih.gov/pubmed/31595012
http://dx.doi.org/10.1038/s41598-019-50430-7
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author Kim, Kyungsook
Bou-Ghannam, Sophia
Thorp, Hallie
Grainger, David W.
Okano, Teruo
author_facet Kim, Kyungsook
Bou-Ghannam, Sophia
Thorp, Hallie
Grainger, David W.
Okano, Teruo
author_sort Kim, Kyungsook
collection PubMed
description Cell-based therapies are increasingly focused on allogeneic stem cell sources because of several advantages in eliminating donor variability (e.g., aging and disease pathophysiology) affecting stem cell quality and in cell-banked sourcing of healthy donors to enable “off-the-shelf” products. However, allogeneic cell therapy is limited by host patient immunologic competence and inconsistent performance due to cell delivery methods. To address allogeneic cell therapy limitations, this study developed a new allogeneic stem cell sheet using human umbilical cord mesenchymal stem cells (hUC-MSC) that present low antigenicity (i.e., major histocompatibility complex, MHC). Optimal conditions including cell density, passage number, and culture time were examined to fabricate reliable hUC-MSC sheets. MHC II antigens correlated to alloimmune rejection were barely expressed in hUC-MSC sheets compared to other comparator MSC sheets (hBMSC and hADSC). hUC-MSC sheets easily graft spontaneously onto subcutaneous tissue in immune-deficient mice within 10 minutes of placement. No sutures are required to secure sheets to tissue because sheet extracellular matrix (ECM) actively facilitates cell-target tissue adhesion. At 10 days post-transplantation, hUC-MSC sheets remain on ectopic target tissue sites and exhibit new blood vessel formation. Furthermore, implanted hUC-MSC sheets secrete human HGF continuously to the murine target tissue. hUC-MSC sheets described here should provide new insights for improving allogenic cell-based therapies.
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spelling pubmed-67834582019-10-16 Human mesenchymal stem cell sheets in xeno-free media for possible allogenic applications Kim, Kyungsook Bou-Ghannam, Sophia Thorp, Hallie Grainger, David W. Okano, Teruo Sci Rep Article Cell-based therapies are increasingly focused on allogeneic stem cell sources because of several advantages in eliminating donor variability (e.g., aging and disease pathophysiology) affecting stem cell quality and in cell-banked sourcing of healthy donors to enable “off-the-shelf” products. However, allogeneic cell therapy is limited by host patient immunologic competence and inconsistent performance due to cell delivery methods. To address allogeneic cell therapy limitations, this study developed a new allogeneic stem cell sheet using human umbilical cord mesenchymal stem cells (hUC-MSC) that present low antigenicity (i.e., major histocompatibility complex, MHC). Optimal conditions including cell density, passage number, and culture time were examined to fabricate reliable hUC-MSC sheets. MHC II antigens correlated to alloimmune rejection were barely expressed in hUC-MSC sheets compared to other comparator MSC sheets (hBMSC and hADSC). hUC-MSC sheets easily graft spontaneously onto subcutaneous tissue in immune-deficient mice within 10 minutes of placement. No sutures are required to secure sheets to tissue because sheet extracellular matrix (ECM) actively facilitates cell-target tissue adhesion. At 10 days post-transplantation, hUC-MSC sheets remain on ectopic target tissue sites and exhibit new blood vessel formation. Furthermore, implanted hUC-MSC sheets secrete human HGF continuously to the murine target tissue. hUC-MSC sheets described here should provide new insights for improving allogenic cell-based therapies. Nature Publishing Group UK 2019-10-08 /pmc/articles/PMC6783458/ /pubmed/31595012 http://dx.doi.org/10.1038/s41598-019-50430-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kim, Kyungsook
Bou-Ghannam, Sophia
Thorp, Hallie
Grainger, David W.
Okano, Teruo
Human mesenchymal stem cell sheets in xeno-free media for possible allogenic applications
title Human mesenchymal stem cell sheets in xeno-free media for possible allogenic applications
title_full Human mesenchymal stem cell sheets in xeno-free media for possible allogenic applications
title_fullStr Human mesenchymal stem cell sheets in xeno-free media for possible allogenic applications
title_full_unstemmed Human mesenchymal stem cell sheets in xeno-free media for possible allogenic applications
title_short Human mesenchymal stem cell sheets in xeno-free media for possible allogenic applications
title_sort human mesenchymal stem cell sheets in xeno-free media for possible allogenic applications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783458/
https://www.ncbi.nlm.nih.gov/pubmed/31595012
http://dx.doi.org/10.1038/s41598-019-50430-7
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