May 2007
Volume 48, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2007
Reconstitution of Conjunctival Epithelium Under the Influence of Mesenchymal Stem Cells in a Symblepharon Rabbit Model
Author Affiliations & Notes
  • E. Gardea
    Service d''ophtalmologie CHU Charles Nicolle, Rouen, France
  • J. Gueudry
    Service d''ophtalmologie CHU Charles Nicolle, Rouen, France
  • C. Duclos
    Service d'anatomie pathologique CHU Charles Nicolle, Rouen, France
  • J. Vannier
    (3) Laboratoire MERCI, EA 3829 Faculté de médecine, Rouen, France
  • J. Marie
    Service d'ORL CHU Charles Nicolle, Rouen, France
  • M. Lamacz
    (3) Laboratoire MERCI, EA 3829 Faculté de médecine, Rouen, France
  • M. Muraine
    Service d''ophtalmologie CHU Charles Nicolle, Rouen, France
  • Footnotes
    Commercial Relationships E. Gardea, None; J. Gueudry, None; C. Duclos, None; J. Vannier, None; J. Marie, None; M. Lamacz, None; M. Muraine, None.
  • Footnotes
    Support None.
Investigative Ophthalmology & Visual Science May 2007, Vol.48, 385. doi:
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      E. Gardea, J. Gueudry, C. Duclos, J. Vannier, J. Marie, M. Lamacz, M. Muraine; Reconstitution of Conjunctival Epithelium Under the Influence of Mesenchymal Stem Cells in a Symblepharon Rabbit Model. Invest. Ophthalmol. Vis. Sci. 2007;48(13):385.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose:: Conjunctival fibrosis pathologies are difficult to treat and often recurrent. A cellular therapy study using mesenchymal stem cells from bone marrow was performed in order to improve the therapeutic results.

Methods:: An original symblepharon rabbit model was created. The fornix was reconstructed with an amniotic covered membrane, either using mesenchymal stem cells (MA/MSC), or conjunctival fibroblasts (MA/Fibro.) or with a single amniotic membrane (MA).

Results:: In the symblepharon model a loss of anatomy occurs with an average depth reduction of 60 % and a loss of function with goblet cell disappearance. After reconstruction, we had an anatomical restoration in both the operated eyes with a depth close to normal 10 ± 2, 11 ± 3 ET 9 ± 2 mm respectively in the MA/MSC, MA and MA/fibroblasts group. The difference between the groups was not considered statistically significant (p>0.05).The analysis of the conjunctival phenotype by immunochemistry MUC5ac showed a statistically higher density (p<0.05) of goblet cells in the MA/MSC 109 ± 25 group, than in the MA 32 ± 10 and MA/fibroblasts 10 ± 5 cells/mm group. Local inflammation, estimated by histological results was lower and similar in the group MA/MSC and MA with an average of 550 ±50 inflammatory cells/mm in the forniceal area than in the MA/fibroblasts group with an average of 1165 ±50 cells/mm.

Conclusions:: Our results suggest the feasibility of a reliable and reproducible conjunctival symblepharon animal model. The anatomy was restored in all 3 groups but the presence of MSC permitted us to find a conjunctival phenotype close to normal partly due to a decrease in local inflammation.

Keywords: conjunctiva • regeneration • inflammation 
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