• Title/Summary/Keyword: reconstruction of corneal epithelium

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A Comparison of Lyophilized Amniotic Membrane with Cryopreserved Amniotic Membrane for the Reconstruction of Rabbit Corneal Epithelium

  • Ahn Jae-Il;Jang In-Keun;Lee Doo-Hoon;Seo Young-Kwon;Yoon Hee-Hoon;Shin Youn-Ho;Kim Jae-Chan;Song Kye-Yong;Lee Hee-Gu;Yang Eun-Kyung;Kim Ki-Ho;Park Jung-Keung
    • Biotechnology and Bioprocess Engineering:BBE
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    • v.10 no.3
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    • pp.262-269
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    • 2005
  • Many researchers have employed cryopreserved amniotic membrane (CAM) in the treatment of a severely damaged cornea, using corneal epithelial cells cultured on an amniotic membrane (AM). In this study, two Teflon rings were made for culturing the cells on the LAM and CAM, and were then used to support the AM, which is referred to in this paper as an Ahn's AM supporter. The primary corneal epithelial cells were obtained from the limbus, using an ex-plantation method. The corneal epithelium could be reconstructed by culturing the third­passage corneal epithelial cells on the AM. A lyophilized amniotic membrane (LAM) has a higher rate of graft take, a longer shelf life, is easier to store, and safer, due to gamma irradiation, than a (AM. The corneal epithelium reconstructed on the LAM and (AM, supported by the two­Teflon rings, was similar to normal corneal epithelium. However, the advantages of the LAM over that of the (AM make the former more useful. The reconstruction model of the corneal epithelium, using AM, is considered as a good in vitro model for transplantation of cornel epithelium into patients with a severely damaged cornea.

Reconstruction of Rabbit Corneal Epithelium using Lyophilized Amniotic Membrane and Dynamic Culture Method (동결건조 양막과 동적배양법을 이용한 토끼 각막 상피층의 재구성)

  • Ahn, Jae-Il;Jang, In-Keun;Shin, Youn-Ho;Seo, Young-Kwon;Yoon, Hee-Hun;Yoon, Mun-Young;Kim, Jae-Chang;Song, Kye-Yong;Lee, Hee-Gu;Yang, Eun-Kyung;Kim, Ki-Ho;Park, Jung-Keug
    • KSBB Journal
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    • v.20 no.4
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    • pp.305-310
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    • 2005
  • Reconstruction of rabbit corneal epithelium was performed through dynamic culture method using self-manufactured amniotic membrane supporter and lyophilized amniotic membrane. Rabbit corneal epithelial cells were cultured and cryopreserved after isolation from limbus, and the cells could be proliferated by passage number 10. The basal layer was well formed, and the epithelium layer was constructed tightly by the increase of cell proliferation and differentiation by dynamic culture method than static culture. Thus, the reconstruction of the corneal epithelium using lyophilized amniotic membrane is considered to be a good in vitro model for transplantation of corneal epithelium to patients with a severely damaged cornea.

Safety and outcomes of subconjunctival allogenic mesenchymal stem cell transplantation in canine experimental corneal defects

  • Kim, Ju-Won;Lee, So-Young;Park, Hee-Myung
    • Korean Journal of Veterinary Research
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    • v.52 no.3
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    • pp.157-162
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    • 2012
  • Corneal injury is very common clinical condition in veterinary medicine and delayed or incomplete corneal healing has the potential of vision loss due to the loss of corneal transparency. For the reconstruction of corneal epithelium, tissue graft and cell transplantation have been prosperously investigated. The purpose of this study was to evaluate the clinical value and short-term safety of application of cultured allogenic mesenchymal stem cells (MSCs) in the treatment of canine experimental corneal defect. Corneal defects were surgically generated in the central corneas of healthy beagle dogs and cultured canine allogenic MSCs were transplanted via subconjunctival injection. Although mean healing time, the rate of epithelial regeneration, and the degree of corneal transparency were not significantly improved after MSC transplantation, significant immune reaction or incompatibility reaction was not detected except transient local irritation. These results propose the possibility of MSC application as a new regenerative medicine in canine ocular disorders.