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Effects of cell seeding technique and cell density on BMP‐2 production in transduced human mesenchymal stem cells

Small animal models have demonstrated the efficacy of ex vivo regional gene therapy using scaffolds loaded with BMP‐2‐expressing mesenchymal stem cells (MSCs). Prior to clinical translation, optimization of seeding techniques of the transduced cells will be important to minimize time and resource ex...

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Autores principales: Collon, Kevin, Bell, Jennifer A., Chang, Stephanie W., Gallo, Matthew C., Sugiyama, Osamu, Marks, Carolyn, Lieberman, Jay R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804863/
https://www.ncbi.nlm.nih.gov/pubmed/35950648
http://dx.doi.org/10.1002/jbm.a.37430
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author Collon, Kevin
Bell, Jennifer A.
Chang, Stephanie W.
Gallo, Matthew C.
Sugiyama, Osamu
Marks, Carolyn
Lieberman, Jay R.
author_facet Collon, Kevin
Bell, Jennifer A.
Chang, Stephanie W.
Gallo, Matthew C.
Sugiyama, Osamu
Marks, Carolyn
Lieberman, Jay R.
author_sort Collon, Kevin
collection PubMed
description Small animal models have demonstrated the efficacy of ex vivo regional gene therapy using scaffolds loaded with BMP‐2‐expressing mesenchymal stem cells (MSCs). Prior to clinical translation, optimization of seeding techniques of the transduced cells will be important to minimize time and resource expenditure, while maximizing cell delivery and BMP‐2 production. No prior studies have investigated cell‐seeding techniques in the setting of transduced cells for gene therapy applications. Using BMP‐2‐expressing transduced adipose‐derived MSCs and a porous ceramic scaffold, this study compared previously described static and dynamic seeding techniques with respect to cell seeding efficiency, uniformity of cell distribution, and in vitro BMP‐2 production. Static and negative pressure seeding techniques demonstrated the highest seeding efficiency, while orbital shaking was associated with the greatest increases in BMP‐2 production per cell. Low density cell suspensions were associated with the highest seeding efficiency and uniformity of cell distribution, and the greatest increases in BMP‐2 production from 2 to 7 days after seeding. Our results highlight the potential for development of an optimized cell density and seeding technique that could greatly reduce the number of MSCs needed to produce therapeutic BMP‐2 levels in clinical situations. Further studies are needed to investigate in vivo effects of cell seeding techniques on bone healing.
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spelling pubmed-98048632023-01-06 Effects of cell seeding technique and cell density on BMP‐2 production in transduced human mesenchymal stem cells Collon, Kevin Bell, Jennifer A. Chang, Stephanie W. Gallo, Matthew C. Sugiyama, Osamu Marks, Carolyn Lieberman, Jay R. J Biomed Mater Res A Research Articles Small animal models have demonstrated the efficacy of ex vivo regional gene therapy using scaffolds loaded with BMP‐2‐expressing mesenchymal stem cells (MSCs). Prior to clinical translation, optimization of seeding techniques of the transduced cells will be important to minimize time and resource expenditure, while maximizing cell delivery and BMP‐2 production. No prior studies have investigated cell‐seeding techniques in the setting of transduced cells for gene therapy applications. Using BMP‐2‐expressing transduced adipose‐derived MSCs and a porous ceramic scaffold, this study compared previously described static and dynamic seeding techniques with respect to cell seeding efficiency, uniformity of cell distribution, and in vitro BMP‐2 production. Static and negative pressure seeding techniques demonstrated the highest seeding efficiency, while orbital shaking was associated with the greatest increases in BMP‐2 production per cell. Low density cell suspensions were associated with the highest seeding efficiency and uniformity of cell distribution, and the greatest increases in BMP‐2 production from 2 to 7 days after seeding. Our results highlight the potential for development of an optimized cell density and seeding technique that could greatly reduce the number of MSCs needed to produce therapeutic BMP‐2 levels in clinical situations. Further studies are needed to investigate in vivo effects of cell seeding techniques on bone healing. John Wiley & Sons, Inc. 2022-08-11 2022-12 /pmc/articles/PMC9804863/ /pubmed/35950648 http://dx.doi.org/10.1002/jbm.a.37430 Text en © 2022 The Authors. Journal of Biomedical Materials Research Part A published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://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 Research Articles
Collon, Kevin
Bell, Jennifer A.
Chang, Stephanie W.
Gallo, Matthew C.
Sugiyama, Osamu
Marks, Carolyn
Lieberman, Jay R.
Effects of cell seeding technique and cell density on BMP‐2 production in transduced human mesenchymal stem cells
title Effects of cell seeding technique and cell density on BMP‐2 production in transduced human mesenchymal stem cells
title_full Effects of cell seeding technique and cell density on BMP‐2 production in transduced human mesenchymal stem cells
title_fullStr Effects of cell seeding technique and cell density on BMP‐2 production in transduced human mesenchymal stem cells
title_full_unstemmed Effects of cell seeding technique and cell density on BMP‐2 production in transduced human mesenchymal stem cells
title_short Effects of cell seeding technique and cell density on BMP‐2 production in transduced human mesenchymal stem cells
title_sort effects of cell seeding technique and cell density on bmp‐2 production in transduced human mesenchymal stem cells
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804863/
https://www.ncbi.nlm.nih.gov/pubmed/35950648
http://dx.doi.org/10.1002/jbm.a.37430
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