Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0050993
Title: Plastic Compressed Collagen as a Novel Carrier for Expanded Human Corneal Endothelial Cells for Transplantation
Authors: Levis H.J.
Peh G.S.L. 
Toh K.-P.
Poh R.
Shortt A.J.
Drake R.A.L.
Mehta J.S. 
Daniels J.T.
Keywords: adenosine triphosphatase (potassium sodium)
biomaterial
collagen
plastic compressed collagen
protein ZO1
unclassified drug
article
cell transfer
clinical protocol
cornea transplantation
Descemet stripping endothelial keratoplasty
endothelium cell
human
human cell
human tissue
immunohistochemistry
in vitro study
microvillus
morphology
organ donor
recipient
tight junction
Adolescent
Animals
Biological Markers
Cell Line
Cell Proliferation
Cell Shape
Cells, Cultured
Collagen
Endothelial Cells
Endothelium, Corneal
Humans
Immunohistochemistry
Plastics
Rats
Sus scrofa
Tissue Scaffolds
Young Adult
Issue Date: 2012
Citation: Levis H.J., Peh G.S.L., Toh K.-P., Poh R., Shortt A.J., Drake R.A.L., Mehta J.S., Daniels J.T. (2012). Plastic Compressed Collagen as a Novel Carrier for Expanded Human Corneal Endothelial Cells for Transplantation. PLoS ONE 7 (11) : e50993. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0050993
Rights: Attribution 4.0 International
Abstract: Current treatments for reversible blindness caused by corneal endothelial cell failure involve replacing the failed endothelium with donor tissue using a one donor-one recipient strategy. Due to the increasing pressure of a worldwide donor cornea shortage there has been considerable interest in developing alternative strategies to treat endothelial disorders using expanded cell replacement therapy. Protocols have been developed which allow successful expansion of endothelial cells in vitro but this approach requires a supporting material that would allow easy transfer of cells to the recipient. We describe the first use of plastic compressed collagen as a highly effective, novel carrier for human corneal endothelial cells. A human corneal endothelial cell line and primary human corneal endothelial cells retained their characteristic cobblestone morphology and expression of tight junction protein ZO-1 and pump protein Na+/K+ ATPase ?1 after culture on collagen constructs for up to 14 days. Additionally, ultrastructural analysis suggested a well-integrated endothelial layer with tightly opposed cells and apical microvilli. Plastic compressed collagen is a superior biomaterial in terms of its speed and ease of production and its ability to be manipulated in a clinically relevant manner without breakage. This method provides expanded endothelial cells with a substrate that could be suitable for transplantation allowing one donor cornea to potentially treat multiple patients. © 2012 Levis et al.
Source Title: PLoS ONE
URI: https://scholarbank.nus.edu.sg/handle/10635/161701
ISSN: 19326203
DOI: 10.1371/journal.pone.0050993
Rights: Attribution 4.0 International
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