Anti-apoptotic gene therapy prolongs survival of corneal endothelial cells during storage

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Anti-apoptotic gene therapy prolongs survival of corneal endothelial cells during storage

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Title: Anti-apoptotic gene therapy prolongs survival of corneal endothelial cells during storage
Author: Fuchsluger, T A; Jurkunas, Ula V.; Kazlauskas, Andrius; Dana, Reza

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Citation: Fuchsluger, T A, U Jurkunas, A Kazlauskas, and R Dana. 2011. “Anti-Apoptotic Gene Therapy Prolongs Survival of Corneal Endothelial Cells During Storage.” Gene Therapy 18 (8) (March 17): 778–787. doi:10.1038/gt.2011.20.
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Abstract: Corneal transplantation is the most common form of grafting performed worldwide. Corneal endothelial cells (EC) form a monolayer in the posterior portion of the cornea and are essential for corneal transparency. EC loss during storage prior to transplantation is a principal reason for rendering donor tissue unsuitable for transplantation, and apoptosis has been shown to be the major contributor to EC loss during storage and after transplantation. Therefore, the potential use of anti-apoptotic gene therapy to promote both graft storage and graft survival is of major interest. The goal of this study was to transduce human donor corneas in vitro to enhance EC survival during storage conditions used in eye banking. We utilized a lentiviral vector to perform gene transfer of baculoviral p35 or mammalian Bcl-xL to corneal endothelium in different storage conditions utilizing a lentiviral vector. Our results show significantly enhanced survival and prolonged retention of physiological EC morphology in cells expressing either p35 or Bcl-xL. The clinical application of this technology could lead to a higher availability of donor tissue for transplantation, extend storage periods, and reduce graft failure after transplantation.
Published Version: 10.1038/gt.2011.20
Other Sources: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3587653/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:34388123
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