May 2004
Volume 45, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2004
Expression of nervous tissue–specific proteoglycans in the retina after transplantation of neural precursor cells.
Author Affiliations & Notes
  • Y. Mawatari
    Department of Ophthalmology and Visual Science, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan
  • M. Fukushima
    Department of Ophthalmology and Visual Science, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan
  • T. Inoue
    Department of Ophthalmology and Visual Science, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan
    Department of Cell Fate Modulation, Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto, Japan
  • T. Taga
    Department of Cell Fate Modulation, Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto, Japan
  • H. Tanihara
    Department of Ophthalmology and Visual Science, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan
  • Footnotes
    Commercial Relationships  Y. Mawatari, None; M. Fukushima, None; T. Inoue, None; T. Taga, None; H. Tanihara, None.
  • Footnotes
    Support  none
Investigative Ophthalmology & Visual Science May 2004, Vol.45, 5393. doi:
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    • Get Citation

      Y. Mawatari, M. Fukushima, T. Inoue, T. Taga, H. Tanihara; Expression of nervous tissue–specific proteoglycans in the retina after transplantation of neural precursor cells. . Invest. Ophthalmol. Vis. Sci. 2004;45(13):5393.

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

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Abstract

Abstract: : Purpose:Nervous tissue–specific proteoglycans are suggested to play important roles in cell adhesion and proliferation, differentiation, axonal growth, and axonal pathfinding during development of the nervous system. After brain or retinal injury, nervous tissue–specific proteoglycans are upregurated in the glial scar. This study was conducted in an attempt to investigate the expression of nervous tissue specific proteoglycan in retina after transplantation of neural precursor cells (NPCs). Method: N–methyl–D–aspartate (NMDA; 4mM, 5µl) was injected into the intravitreal space of adult rat to induce retinal cell death. NPCs were prepared from the telencephalic neuroepithelium of EGFP (enhanced green fluorescence protein) transgenic mice on embryonic day 14. Cell suspension (5x105 cells) was injected into intravitreal space of NMDA–treated eyes. At 1, 2 or 4 week after transplantation, sections were prepared for immunohistochemistry of nervous tissue–specific proteoglycans (neurocan, phosphacan, and neuroglycan C). Results: The expression of nervous tissue–specific proteoglycans is abundant in developing rat retina, but is only faint in mature retina. These proteoglycans were expressed in inner plexiform layer and outer plexiform layer in the host mature retina with incorporation of NPCs. Furthermore the neurites of some incorporated NPCs expressed these proteoglycans. Conclusion: We demonstrated that the upregulated expression of nervous tissue specific proteoglycan in the retina after transplantation of NPCs. The results suggest that the proteoglycan may play a role in differentiation and axonal growth of NPCs in the host retina.

Keywords: transplantation • proteoglycans/glycosaminoglycans • immunohistochemistry 
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