Gene therapy for retinal ganglion cell neuroprotection in glaucoma

被引:66
作者
Wilson, A. M. [1 ,2 ]
Di Polo, A. [1 ,2 ,3 ]
机构
[1] Univ Montreal, Dept Pathol & Cell Biol, Montreal, PQ H3T 1J4, Canada
[2] Univ Montreal, Grp Rech Syst Nerveux Cent, Montreal, PQ H3T 1J4, Canada
[3] Univ Montreal, Dept Ophthalmol, Montreal, PQ H3T 1J4, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
retinal ganglion cell; neuroprotection; glaucoma; CILIARY NEUROTROPHIC FACTOR; CENTRAL-NERVOUS-SYSTEM; POSTSYNAPTIC TARGET NEURONS; LATERAL GENICULATE-NUCLEUS; AXOTOMY-INDUCED APOPTOSIS; IN-VIVO; AXON REGENERATION; C-JUN; ANTISENSE OLIGONUCLEOTIDES; TRANSGENE EXPRESSION;
D O I
10.1038/gt.2011.142
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glaucoma is the leading cause of irreversible blindness worldwide. The primary cause of glaucoma is not known, but several risk factors have been identified, including elevated intraocular pressure and age. Loss of vision in glaucoma is caused by the death of retinal ganglion cells (RGCs), the neurons that convey visual information from the retina to the brain. Therapeutic strategies aimed at delaying or halting RGC loss, known as neuroprotection, would be valuable to save vision in glaucoma. In this review, we discuss the significant progress that has been made in the use of gene therapy to understand mechanisms underlying RGC degeneration and to promote the survival of these neurons in experimental models of optic nerve injury. Gene Therapy (2012) 19, 127-136; doi:10.1038/gt.2011.142; published online 6 October 2011
引用
收藏
页码:127 / 136
页数:10
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