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The Favorable Effect of Mesenchymal Stem Cell Treatment on the Antioxidant Protective Mechanism in the Corneal Epithelium and Renewal of Corneal Optical Properties Changed after Alkali Burns
C. Cejka, V. Holan, P. Trosan, A. Zajicova, E. Javorkova, J. Cejkova,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 2008
Hindawi Publishing Open Access
from 2008-01-01
PubMed Central
from 2008
Europe PubMed Central
from 2008
ProQuest Central
from 2014-01-01
Open Access Digital Library
from 2008-01-01
Open Access Digital Library
from 2008-01-01
Open Access Digital Library
from 2009-01-01
Medline Complete (EBSCOhost)
from 2011-01-01
Health & Medicine (ProQuest)
from 2014-01-01
PubMed
27057279
DOI
10.1155/2016/5843809
Knihovny.cz E-resources
- MeSH
- Alkalies MeSH
- Antioxidants therapeutic use MeSH
- Cell Differentiation drug effects MeSH
- Burns, Chemical enzymology genetics pathology therapy MeSH
- Immunohistochemistry MeSH
- Rabbits MeSH
- Limbus Corneae cytology MeSH
- Matrix Metalloproteinase 9 metabolism MeSH
- Mesenchymal Stem Cells cytology drug effects MeSH
- Protective Agents pharmacology therapeutic use MeSH
- Corneal Pachymetry MeSH
- Gene Expression Regulation drug effects MeSH
- Epithelium, Corneal pathology MeSH
- Superoxide Dismutase metabolism MeSH
- Nitric Oxide Synthase Type II metabolism MeSH
- Transforming Growth Factor beta genetics metabolism MeSH
- Mesenchymal Stem Cell Transplantation * MeSH
- Adipocytes cytology drug effects MeSH
- Vascular Endothelial Growth Factor A metabolism MeSH
- Corneal Opacity complications therapy MeSH
- Animals MeSH
- Check Tag
- Rabbits MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
The aim of this study was to examine whether mesenchymal stem cells (MSCs) and/or corneal limbal epithelial stem cells (LSCs) influence restoration of an antioxidant protective mechanism in the corneal epithelium and renewal of corneal optical properties changed after alkali burns. The injured rabbit corneas (with 0.25 N NaOH) were untreated or treated with nanofiber scaffolds free of stem cells, with nanofiber scaffolds seeded with bone marrow MSCs (BM-MSCs), with adipose tissue MSCs (Ad-MSCs), or with LSCs. On day 15 following the injury, after BM-MSCs or LSCs nanofiber treatment (less after Ad-MSCs treatment) the expression of antioxidant enzymes was restored in the regenerated corneal epithelium and the expressions of matrix metalloproteinase 9 (MMP9), inducible nitric oxide synthase (iNOS), α-smooth muscle actin (α-SMA), transforming growth factor-β1 (TGF-β1), and vascular endothelial factor (VEGF) were low. The central corneal thickness (taken as an index of corneal hydration) increased after the injury and returned to levels before the injury. In injured untreated corneas the epithelium was absent and numerous cells revealed the expressions of iNOS, MMP9, α-SMA, TGF-β1, and VEGF. In conclusion, stem cell treatment accelerated regeneration of the corneal epithelium, restored the antioxidant protective mechanism, and renewed corneal optical properties.
References provided by Crossref.org
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