April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Different Unfolded protein response pathway activation involved in three kinds of cataract
Author Affiliations & Notes
  • Jing Yang
    Zhongshan Ophthalmic Center, Guangzhou, China
  • Sheng Zhou
    Zhongshan Ophthalmic Center, Guangzhou, China
  • Jianjun Gu
    Zhongshan Ophthalmic Center, Guangzhou, China
  • Footnotes
    Commercial Relationships Jing Yang, None; Sheng Zhou, None; Jianjun Gu, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 6029. doi:
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      Jing Yang, Sheng Zhou, Jianjun Gu; Different Unfolded protein response pathway activation involved in three kinds of cataract. Invest. Ophthalmol. Vis. Sci. 2014;55(13):6029.

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

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Abstract

Purpose: More and more research demonstrated that unfolded protein response is involved in the cataract formation. Since there are so many differences on pathogenesis and clinical manifestation among age related, congenital and high myopia related cataract, the purpose of our experiment is to explore whether UPR is involved in the pathogenesis of these three kinds of cataract, and their UPR pathway activation difference.

Methods: Using lens anterior capsular samples from four different groups (normal people, age related cataract, congenital and high myopia related cataract group), we show that the lens exhibited different activation of IRE1, ATF6, and PERK associated UPR pathway among these groups.

Results: Compared with normal people group, high myopia related and age related cataract group have significantly increased IRE1A and EIF2α expression, while congenital cataract group has only significantly increased IRE1A. There was no significant difference of ATF6 expression within the four groups.

Conclusions: Our result indicated that UPR is involved in all of these three kinds of cataract formation, but their activation pathways are variant.

Keywords: 445 cataract • 533 gene/expression • 659 protein structure/function  
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