4.3 Article

Cyclooxygenase-2 plays a critical role in retinal ganglion cell death after transient ischemia: Real-time monitoring of RGC survival using Thy-1-EGFP transgenic mice

期刊

NEUROSCIENCE RESEARCH
卷 65, 期 4, 页码 319-325

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.neures.2009.08.008

关键词

COX-2; Thy-1-EGFP; Retina; Cell death; Retinal ganglion cell; Transgenic mouse; Knockout mouse

资金

  1. Ministry of Health, Labour and Welfare of Japan

向作者/读者索取更多资源

The exact role of cyclooxygenase-2 (COX-2) in neurodegeneration of retinal ganglion cells (RGCs) in vivo following ischemia-reperfusion injury of the retina was unknown. We made transgenic mice in which the Thy-1.2 promoter drives the expression of EGFP cDNA (Thy-1-EGFP) in RGCs to monitor RGC survival and death in retinal whole mount preparations and in live animals. We show that celecoxib, a selective COX-2 inhibitor, blocks RGC death after ischemic injury. Furthermore, in COX-2 knockout (COX-2(-/-)) mice, RGCs are resistant to ischemia-reperfusion injury. Finally, we performed time-lapse monitoring of RGC death after ischemia in Thy-1-EGFP; COX-2(-/-) mice. Our data show that COX-2 plays a crucial role in ischemia-reperfusion injury-induced RGC death. Inhibition of COX-2 activity may therefore be an effective therapy for neurodegenerative diseases of the retina and optic nerve. (C) 2009 Elsevier Ireland Ltd and the Japan Neuroscience Society. All rights reserved.

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