論文

査読有り
2008年

Involvement of retinal neurons and pigment epithelial cells in a murine model of Sandhoff disease

OPHTHALMIC RESEARCH
  • Kazunori Sango
  • ,
  • Shoji Yamanaka
  • ,
  • Kyoko Ajiki
  • ,
  • Nobutaka Arai
  • ,
  • Masahiko Takano

40
5
開始ページ
241
終了ページ
248
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1159/000127831
出版者・発行元
KARGER

Background/Aims: To investigate the effects of deficient degradation of glycolipids on the morphological appearance of all retinal cells in a murine model of G(M2) gangliosidosis (Sandhoff disease). Methods: The morphological appearance of the retina in Sandhoff mice at symptomatic stages (3 and 4 months of age) was examined by immunohistochemistry, lectin histochemistry and electron microscopy. Results: Under a light microscope, intense immunoreactivity for G(M2) ganglioside was observed in the ganglion cell, inner plexiform, and inner nuclear layers in the Sandhoff mice. The ganglion cell layers and retinal pigment epithelium in the Sandhoff mice were stained intensely with concanavalin A agglutinin and succinylated wheat germ agglutinin. Ultrastructural studies revealed numerous inclusions in the cytoplasm of retinal ganglion cells and other neuronal cells (particularly amacrine cells), whereas we failed to detect apparent involvement of photoreceptor cells. In addition to the cytoplasmic inclusions in the retinal neurons, vacuolation was evident in the retinal pigment epithelium. Conclusion: These findings suggest that neuronal cells and pigment epithelial cells are more vulnerable to the deficient ganglioside degradation than other retinal cells in Sandhoff mice. Copyright (C) 2008 S. Karger AG, Basel.

リンク情報
DOI
https://doi.org/10.1159/000127831
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/18437034
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000258318600005&DestApp=WOS_CPL
ID情報
  • DOI : 10.1159/000127831
  • ISSN : 0030-3747
  • PubMed ID : 18437034
  • Web of Science ID : WOS:000258318600005

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