May 2007
Volume 48, Issue 13
ARVO Annual Meeting Abstract  |   May 2007
A Role of µ-Crystallin in Endotoxin-Induced Uveitis
Author Affiliations & Notes
  • H. Imai
    Shinshu University, Matsumoto, Japan
  • K. Ohta
    Shinshu University, Matsumoto, Japan
  • A. Yoshida
    Ophthalmology, Shinshu university, Matsumoto, Japan
  • S. Suzuki
    Aging Medicine and Geriatrics, Aging and Adaptation,Shinshu University Graduate School, Matsumoto, Japan
  • T. Kikuchi
    Shinshu University, Matsumoto, Japan
    Research center for Human and Enviromental Sciences,
  • Footnotes
    Commercial Relationships H. Imai, None; K. Ohta, None; A. Yoshida, None; S. Suzuki, None; T. Kikuchi, None.
  • Footnotes
    Support None.
Investigative Ophthalmology & Visual Science May 2007, Vol.48, 2635. doi:
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      H. Imai, K. Ohta, A. Yoshida, S. Suzuki, T. Kikuchi; A Role of µ-Crystallin in Endotoxin-Induced Uveitis. Invest. Ophthalmol. Vis. Sci. 2007;48(13):2635.

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

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Purpose:: µ-Crystallin (CRYM) was first identified as a major structural protein of lens. We have previously reported that CRYM was highly expressed in iris-ciliary body (ICB) of endotoxin-induced uveitis(EIU) rats by cDNA microarray analysis. This indicated that CRYM probably had non-crystallin role, like other crystallins. The purpose of this study was to examine a possible role of CRYM in EIU.

Methods:: EIU was induced by a footpad injection of lipopolisaccaride (LPS) in male Lewis rats (6~8 week). The expression level of CRYM expression in the ICB at each time point (3, 6, 12, 24) after LPS injection was studied by real time RT-PCR and Western blot analysis. Immunohistochemical studies were also performed to localize CRYM. Eyes of C57BL/6J (B6) mice and CRYM deficient (CRYM-KO)mice were enucleated on 5 days after LPS injection. Inflammatory cells infiltrated into the anterior chamber (AC) and vitreous cavity were counted on histologic sections of eyes.

Results:: CRYM mRNA was up-regulated in the ICB at 6, 12 hours after LPS injection. CRYM protein up-regulated at 12, 24, 48 hours after LPS injection, and identified in the non-pigment ciliary epithelium. The number (mean ± S. E. M) of inflammatory cells infiltrated into the AC and vitreous body of CRYM-KO mice were significantly less than those of B6 mice (6.1 ± 1.2 , 16.1 ± 1.6 cells/section, respectively).

Conclusions:: CRYM was expressed in the non-pigment ciliary epithelium in EIU. Intraocular inflammation in CRYM-KO mice was milder compared with that in control. These results suggested CRYM might be associated to recurrent of late inflammatory cells or delay inflammation.

Keywords: uveitis-clinical/animal model • crystallins • inflammation 

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