Outcome of transplanted mesenchymal stem cells in the alkali burned cornea

Purpose: Mesenchymal stem cells show promising results in cell therapy for many medical fields. We aimed to study their fate when transplanted in the inflammatory corneal environnement: survival, migration towards the injured tissues, differenciation.Methods: Plastic-adherent, mononucleate cells der...

Full description

Saved in:
Bibliographic Details
Published inActa ophthalmologica (Oxford, England) Vol. 86; no. s243
Main Authors VERA, L, LATOUCHE, JB, GUEUDRY, J, VANNIER, JP, MURAINE, M
Format Journal Article
LanguageEnglish
Published 01.09.2008
Online AccessGet full text

Cover

Loading…
More Information
Summary:Purpose: Mesenchymal stem cells show promising results in cell therapy for many medical fields. We aimed to study their fate when transplanted in the inflammatory corneal environnement: survival, migration towards the injured tissues, differenciation.Methods: Plastic-adherent, mononucleate cells derived from the bone marrow of New Zealand White rabbits, were transfected with Green Fluorescent Protein (GFP) and expanded in cultures. These MSCs were injected either directly in the stroma, or in the sub-conjunctival space, six hours after the alkali burn of the center of the cornea. Immunohistochemistry and immnunofluorescence were performed one week to four weeks after the transplantation.Results: MSCs were detected by fluorescence microscopy at 7 days and 14 days after transplantation, whatever the site of injection. They were not present in our cut sections after two weeks. After the sub-conjunctival injection, they were mostly localized at the limbus and the peripheral cornea. When transplanted directly in the stroma, they were more dispersed and remained at the site of injection. Fourteen days after transplantation, more than 90% of the MSCs expressed the a- smooth muscle actin marker, like residual keratocytes .MSCs never integrated the epithelial layers and did not express cytokeratins. Conclusion: These results suggest that MSCs transfected with GFP can migrate towards the damaged tissue when injected in the sub-conjunctival space and survive during at least two weeks. They engraft to stromal cornea and differenciate rapidly into myofibroblasts. These MSCs are not able to differenciate into epithelial cells in our model.Their differenciation into myofibroblasts suggests that they might be involved in the stromal wound healing.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1755-375X
1755-3768
DOI:10.1111/j.1755-3768.2008.542.x