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The effects of Rho-associated kinase inhibitor Y-27632 on primary human corneal endothelial cells propagated using a dual media approach

The global shortage of donor corneas has garnered extensive interest in the development of graft alternatives suitable for endothelial keratoplasty using cultivated primary human corneal endothelial cells (CECs). We have recently described a dual media approach for the propagation of human CECs. In...

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Autores principales: Peh, Gary S. L., Adnan, Khadijah, George, Benjamin L., Ang, Heng-Pei, Seah, Xin-Yi, Tan, Donald T., Mehta, Jodhbir S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4387913/
https://www.ncbi.nlm.nih.gov/pubmed/25823914
http://dx.doi.org/10.1038/srep09167
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author Peh, Gary S. L.
Adnan, Khadijah
George, Benjamin L.
Ang, Heng-Pei
Seah, Xin-Yi
Tan, Donald T.
Mehta, Jodhbir S.
author_facet Peh, Gary S. L.
Adnan, Khadijah
George, Benjamin L.
Ang, Heng-Pei
Seah, Xin-Yi
Tan, Donald T.
Mehta, Jodhbir S.
author_sort Peh, Gary S. L.
collection PubMed
description The global shortage of donor corneas has garnered extensive interest in the development of graft alternatives suitable for endothelial keratoplasty using cultivated primary human corneal endothelial cells (CECs). We have recently described a dual media approach for the propagation of human CECs. In this work, we characterize the effects of a Rho-kinase inhibitor Y-27632 on the cultivation of CECs propagated using the dual media culture system. Seventy donor corneas deemed unsuitable for transplantation were procured for this study. We assessed the use of Y-27632 for its effect at each stage of the cell culture process, specifically for cell attachment, cell proliferation, and during both regular passaging and cryopreservation. Lastly, comparison of donor-matched CEC-cultures expanded with or without Y-27632 was also performed. Our results showed that Y-27632 significantly improved the attachment and proliferation of primary CECs. A non-significant pro-survival effect was detected during regular cellular passage when CECs were pre-treated with Y-27632, an effect that became more evident during cryopreservation. Our study showed that the inclusion of Y-27632 was beneficial for the propagation of primary CECs expanded via the dual media approach, and was able to increase overall cell yield by between 1.96 to 3.36 fold.
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spelling pubmed-43879132015-04-08 The effects of Rho-associated kinase inhibitor Y-27632 on primary human corneal endothelial cells propagated using a dual media approach Peh, Gary S. L. Adnan, Khadijah George, Benjamin L. Ang, Heng-Pei Seah, Xin-Yi Tan, Donald T. Mehta, Jodhbir S. Sci Rep Article The global shortage of donor corneas has garnered extensive interest in the development of graft alternatives suitable for endothelial keratoplasty using cultivated primary human corneal endothelial cells (CECs). We have recently described a dual media approach for the propagation of human CECs. In this work, we characterize the effects of a Rho-kinase inhibitor Y-27632 on the cultivation of CECs propagated using the dual media culture system. Seventy donor corneas deemed unsuitable for transplantation were procured for this study. We assessed the use of Y-27632 for its effect at each stage of the cell culture process, specifically for cell attachment, cell proliferation, and during both regular passaging and cryopreservation. Lastly, comparison of donor-matched CEC-cultures expanded with or without Y-27632 was also performed. Our results showed that Y-27632 significantly improved the attachment and proliferation of primary CECs. A non-significant pro-survival effect was detected during regular cellular passage when CECs were pre-treated with Y-27632, an effect that became more evident during cryopreservation. Our study showed that the inclusion of Y-27632 was beneficial for the propagation of primary CECs expanded via the dual media approach, and was able to increase overall cell yield by between 1.96 to 3.36 fold. Nature Publishing Group 2015-03-16 /pmc/articles/PMC4387913/ /pubmed/25823914 http://dx.doi.org/10.1038/srep09167 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Peh, Gary S. L.
Adnan, Khadijah
George, Benjamin L.
Ang, Heng-Pei
Seah, Xin-Yi
Tan, Donald T.
Mehta, Jodhbir S.
The effects of Rho-associated kinase inhibitor Y-27632 on primary human corneal endothelial cells propagated using a dual media approach
title The effects of Rho-associated kinase inhibitor Y-27632 on primary human corneal endothelial cells propagated using a dual media approach
title_full The effects of Rho-associated kinase inhibitor Y-27632 on primary human corneal endothelial cells propagated using a dual media approach
title_fullStr The effects of Rho-associated kinase inhibitor Y-27632 on primary human corneal endothelial cells propagated using a dual media approach
title_full_unstemmed The effects of Rho-associated kinase inhibitor Y-27632 on primary human corneal endothelial cells propagated using a dual media approach
title_short The effects of Rho-associated kinase inhibitor Y-27632 on primary human corneal endothelial cells propagated using a dual media approach
title_sort effects of rho-associated kinase inhibitor y-27632 on primary human corneal endothelial cells propagated using a dual media approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4387913/
https://www.ncbi.nlm.nih.gov/pubmed/25823914
http://dx.doi.org/10.1038/srep09167
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