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Engineering thick cell sheets by electrochemical desorption of oligopeptides on membrane substrates
We developed a gold-coated membrane substrate modified with an oligopeptide layer that can be used to grow and subsequently detach a thick cell sheet through an electrochemical reaction. The oligopeptide CCRRGDWLC was designed to contain a cell adhesive domain (RGD) in the center and cysteine residu...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Japanese Society for Regenerative Medicine
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6581802/ https://www.ncbi.nlm.nih.gov/pubmed/31245469 http://dx.doi.org/10.1016/j.reth.2015.12.003 |
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author | Enomoto, Junko Mochizuki, Naoto Ebisawa, Katsumi Osaki, Tatsuya Kageyama, Tatsuto Myasnikova, Dina Nittami, Tadashi Fukuda, Junji |
author_facet | Enomoto, Junko Mochizuki, Naoto Ebisawa, Katsumi Osaki, Tatsuya Kageyama, Tatsuto Myasnikova, Dina Nittami, Tadashi Fukuda, Junji |
author_sort | Enomoto, Junko |
collection | PubMed |
description | We developed a gold-coated membrane substrate modified with an oligopeptide layer that can be used to grow and subsequently detach a thick cell sheet through an electrochemical reaction. The oligopeptide CCRRGDWLC was designed to contain a cell adhesive domain (RGD) in the center and cysteine residues at both terminals. Cysteine contains a thiol group that forms a gold–thiolate bond on a gold surface. Cells attached to gold-coated membrane substrates via the oligopeptide layer were readily and noninvasively detached by applying a negative electrical potential to cleave the gold–thiolate bond. Because of the effective oxygen supply, fibroblasts vigorously grew on the membrane substrate and the thickness of the cell sheets was ∼60 μm at 14 days of culture, which was 2.9-fold greater than that of cells grown on a conventional culture dish. The cell sheets were detached after 7 min of electrical potential application. Using this approach, five layers of cell sheets were stacked sequentially with thicknesses reaching >200 μm. This approach was also beneficial for rapidly and readily transplanting cell sheets. Grafted cell sheets secreted collagen and remained at the transplanted site for at least 2 months after transplantation. This simple electrochemical cell sheet engineering technology is a promising tool for tissue engineering and regenerative medicine applications. |
format | Online Article Text |
id | pubmed-6581802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Japanese Society for Regenerative Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-65818022019-06-26 Engineering thick cell sheets by electrochemical desorption of oligopeptides on membrane substrates Enomoto, Junko Mochizuki, Naoto Ebisawa, Katsumi Osaki, Tatsuya Kageyama, Tatsuto Myasnikova, Dina Nittami, Tadashi Fukuda, Junji Regen Ther Original Article We developed a gold-coated membrane substrate modified with an oligopeptide layer that can be used to grow and subsequently detach a thick cell sheet through an electrochemical reaction. The oligopeptide CCRRGDWLC was designed to contain a cell adhesive domain (RGD) in the center and cysteine residues at both terminals. Cysteine contains a thiol group that forms a gold–thiolate bond on a gold surface. Cells attached to gold-coated membrane substrates via the oligopeptide layer were readily and noninvasively detached by applying a negative electrical potential to cleave the gold–thiolate bond. Because of the effective oxygen supply, fibroblasts vigorously grew on the membrane substrate and the thickness of the cell sheets was ∼60 μm at 14 days of culture, which was 2.9-fold greater than that of cells grown on a conventional culture dish. The cell sheets were detached after 7 min of electrical potential application. Using this approach, five layers of cell sheets were stacked sequentially with thicknesses reaching >200 μm. This approach was also beneficial for rapidly and readily transplanting cell sheets. Grafted cell sheets secreted collagen and remained at the transplanted site for at least 2 months after transplantation. This simple electrochemical cell sheet engineering technology is a promising tool for tissue engineering and regenerative medicine applications. Japanese Society for Regenerative Medicine 2016-03-01 /pmc/articles/PMC6581802/ /pubmed/31245469 http://dx.doi.org/10.1016/j.reth.2015.12.003 Text en © 2016, The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Enomoto, Junko Mochizuki, Naoto Ebisawa, Katsumi Osaki, Tatsuya Kageyama, Tatsuto Myasnikova, Dina Nittami, Tadashi Fukuda, Junji Engineering thick cell sheets by electrochemical desorption of oligopeptides on membrane substrates |
title | Engineering thick cell sheets by electrochemical desorption of oligopeptides on membrane substrates |
title_full | Engineering thick cell sheets by electrochemical desorption of oligopeptides on membrane substrates |
title_fullStr | Engineering thick cell sheets by electrochemical desorption of oligopeptides on membrane substrates |
title_full_unstemmed | Engineering thick cell sheets by electrochemical desorption of oligopeptides on membrane substrates |
title_short | Engineering thick cell sheets by electrochemical desorption of oligopeptides on membrane substrates |
title_sort | engineering thick cell sheets by electrochemical desorption of oligopeptides on membrane substrates |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6581802/ https://www.ncbi.nlm.nih.gov/pubmed/31245469 http://dx.doi.org/10.1016/j.reth.2015.12.003 |
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