April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Macrophage expressing oxidative stress marker play some role in lacrimal gland of chronic graft-versus-host disease
Author Affiliations & Notes
  • Yoko Ogawa
    Department of Ophthalmology, Keio Univ School of Medicine, Shinjuku-Ku, Japan
  • Shigeto Shimmura
    Department of Ophthalmology, Keio Univ School of Medicine, Shinjuku-Ku, Japan
  • Takanori Suzuki
    Department of Ophthalmology, Keio Univ School of Medicine, Shinjuku-Ku, Japan
  • Masataka Kawai
    Department of Ophthalmology, Keio Univ School of Medicine, Shinjuku-Ku, Japan
  • Kazuo Tsubota
    Department of Ophthalmology, Keio Univ School of Medicine, Shinjuku-Ku, Japan
  • Footnotes
    Commercial Relationships Yoko Ogawa, None; Shigeto Shimmura, None; Takanori Suzuki, None; Masataka Kawai, None; Kazuo Tsubota, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 494. doi:
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      Yoko Ogawa, Shigeto Shimmura, Takanori Suzuki, Masataka Kawai, Kazuo Tsubota, Department of Ophthalmology, Keio University School of Medicine; Macrophage expressing oxidative stress marker play some role in lacrimal gland of chronic graft-versus-host disease. Invest. Ophthalmol. Vis. Sci. 2014;55(13):494.

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

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Abstract

Purpose: To investigate whether immune aging are involved in the lacrimal glands of cGVHD .

Methods: We obtained the specimens from cGVHD model mice, untreated aged and young mice, and examined by histopathology using fluoresecent imaging and transmissin electron microscopy, and immunoblotting. Molecules associated with T cell activation, senescenct phenotype, oxidative stress, and other aging, especially p16 were examined to assess the samples. Characterization of immune cells expressing cellular senescent markers were also assessed by immunofluorescent double staining.

Results: Immune blotting revealed cGVHD lacrimal glands exhibited high expression of oxidative stress markers similar to those in aging mice, but not in young mice. Double staining of immune cells and senescent associated molecules showed T cells interacted with inflammatory cells expressing senescent markers, which were confirmed as CD68+ macrophages. In addition, macrophages expressed MHC class II and CD40, suggesting that macrophages act as antigen presenting cells in the animal model of lacrimal gland cGVHD.

Conclusions: These results suggest that senescent macrophages might contribute to the development of immune mediated dry eye disease.

Keywords: 413 aging • 576 lacrimal gland • 555 immunomodulation/immunoregulation  
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