色素性视网膜炎
视网膜变性
感光细胞
人类视网膜的基因治疗
视网膜
变性(医学)
视网膜色素上皮
视网膜
生物
黄斑变性
梅尔特克
鹌鹑
病理
医学
神经科学
眼科
受体酪氨酸激酶
细胞生物学
激酶
内分泌学
作者
Xin Liu,Yan Zhang,Yuxi He,Jinsong Zhao,Guanfang Su
出处
期刊:PubMed
日期:2015-07-01
卷期号:30 (7): 771-9
被引量:14
摘要
Retinitis pigmentosa is a major cause of visual impairment and blindness, affecting millions of people worldwide. The mechanisms of and effective treatments for the disease, however, remain to be further investigated. The Royal College of Surgeons rat is one of the most widely used animal models for the study of retinal degeneration diseases. The mutation in the mer tyrosine kinase proto-oncogene of this model leads to deficient phagocytosis in the retinal pigment epithelium cells and the accumulation of photoreceptor out segments in the subretinal space, ultimately resulting in retinal degeneration. The retina begins to change as early as 17 days after birth and becomes gradually thinner with the death and remodeling of cells and blood vessels. Retinal cell apoptosis plays a dominant role in this degeneration, with some cells being activated by the secondary alterations of the retinal neurotransmitter and other related factors.
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