May 2005
Volume 46, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2005
Expression and Tissue Distribution of Extracellular Matrix Proteins in Schwalbe’s Line
Author Affiliations & Notes
  • Y. Ikeda
    Department of Opthalmology, Kyoto Prefectural Univercity, Kyoto, Japan
  • S. Kawasaki
    Department of Opthalmology, Kyoto Prefectural Univercity, Kyoto, Japan
  • K. Mori
    Department of Opthalmology, Kyoto Prefectural Univercity, Kyoto, Japan
  • H. Tanioka
    Department of Opthalmology, Kyoto Prefectural Univercity, Kyoto, Japan
  • S. Naruse
    Department of Opthalmology, Kyoto Prefectural Univercity, Kyoto, Japan
  • T. Ikushima
    Department of Opthalmology, Kyoto Prefectural Univercity, Kyoto, Japan
  • S. Kinoshita
    Department of Opthalmology, Kyoto Prefectural Univercity, Kyoto, Japan
  • Footnotes
    Commercial Relationships  Y. Ikeda, None; S. Kawasaki, None; K. Mori, None; H. Tanioka, None; S. Naruse, None; T. Ikushima, None; S. Kinoshita, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science May 2005, Vol.46, 3696. doi:
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      Y. Ikeda, S. Kawasaki, K. Mori, H. Tanioka, S. Naruse, T. Ikushima, S. Kinoshita; Expression and Tissue Distribution of Extracellular Matrix Proteins in Schwalbe’s Line . Invest. Ophthalmol. Vis. Sci. 2005;46(13):3696.

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

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Abstract

Abstract: : Purpose: Schwalbe’s line (SL), which provides a border between trabecular meshwork (TM) and corneal endothelium, is thought to be a kind of mesenchymal remnant. In this study, we sought to investigate the expression of extracellular matrix (ECM) and related proteins within the SL of normal human eyes in order to further understand its biological role. Methods: Six fresh normal human corneo–scleral tissues (3 males and 3 females; 64.8 ± 11.3 years) , were obtained from a US eye–bank, cryo–embedded and subjected to indirect immunohistochemical analysis. The localization of collagens I, II, III, IVα2, VI, VII, fibronectin, heparan sulfate, laminin V, pan–cytokeratin, vimentin, elastin, and integrin ß1, ß4, α6 were examined. Results: The SL demonstrated strong immunostaining for collagens I, III, IVα2, VI, vimentin, moderate staining for fibronectin, laminin V, elastin, and faint staining for collagens II, VII, heparin sulfate, pan–cytokeratin and integrinß1, ß4, α6. The expression patterns of these ECM proteins and vimentin in the SL were quite similar to those of found within the TM. Conclusions: Abundant expression of collagens I, III, IVα2,VI and vimentin in the SL and TM suggests that these ECM proteins possibly play pivotal roles in maintaining the highly integrated structure of both these tissues. Furthermore, the consistent expression pattern of the ECM proteins and vimentin imply a biological similarity between SL and TM.

Keywords: extraocular muscles: development • trabecular meshwork 
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