April 2010
Volume 51, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2010
Stem Cell Engraft Into Subretinal Space of the Retinal Pigment Epithelium Degenerative Retina
Author Affiliations & Notes
  • J. Lee
    Medicine of anatomy, catholic university, Seoul, Republic of Korea
  • F.-S. Quan
    Medicine of Anatomy, Catholic University, Seoul, Republic of Korea
  • J.-M. Shin
    Medicine of Anatomy, Catholic University, Seoul, Republic of Korea
  • M. Chun
    Medicine of Anatomy, Catholic University, Seoul, Republic of Korea
  • S.-J. Oh
    Medicine of Anatomy, Catholic University, Seoul, Republic of Korea
  • Footnotes
    Commercial Relationships  J. Lee, None; F.-S. Quan, None; J.-M. Shin, None; M. Chun, None; S.-J. Oh, None.
  • Footnotes
    Support  This study was supported by the Ministry of Knowledge Economy, Republic of Korea (10030064).
Investigative Ophthalmology & Visual Science April 2010, Vol.51, 3642. doi:https://doi.org/
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      J. Lee, F.-S. Quan, J.-M. Shin, M. Chun, S.-J. Oh; Stem Cell Engraft Into Subretinal Space of the Retinal Pigment Epithelium Degenerative Retina. Invest. Ophthalmol. Vis. Sci. 2010;51(13):3642. doi: https://doi.org/.

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

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Abstract

Purpose: : The retinal pigment epithelium (RPE) is essential for visual cognition and nutrition of the outer retina. RPE dysfunction is a crucial event to age-related macular degeneration (AMD) and retinitis pigmentosa. To examine the availability of RPE dysfunction model by sodium iodate (SI) administered for the AMD study. Mesenchymal stem cell engraft into subretinal space of this model was tried for a new horizon to therapeutic strategy curing incurable diseases.

Methods: : SI resolved in saline was administered into the peritoneal cavity of the rats in dose of 50 mg/ kg body weight twice with three days interval. DiI-labeled mesenchymal stem cells of 3 passages were applied into the subretinal space of the animals at 4 days after the final injection. RPE degeneration was evaluated by light and electron microscopy and stem cells were traced with immunofluorescent microscopy.

Results: : RPE in the SI-administered retinas was nearly disappeared remaining the continuous basement membrane underneath the choroid. In scanty basal cytoplasm, the melanin pigments and residual bodies were remained. The SI-administered retinas were detached from the RPE remaining opened subretinal space. The outer segments of the photoreceptor cells were shorten. Apoptotic cells with pyknotic nuclei were observed in the outer nuclear layer (ONL) of the SI-administered retinas. Stem cells were largely remained in subretinal space. Some of the stem cells were migrated into the ONL however these migrated cells showed no differentiation into neuronal or glial cell types of the retina.

Conclusions: : These results suggest that an SI-induced RPE degeneration model will be available for AMD pathogenic studies and more researches such as stem cell modification and development of cell carrier substances will be necessary for the stem cell application into subretinal space.

Keywords: age-related macular degeneration • retinal pigment epithelium • injection 
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