HTRA1 过表达诱发老年性黄斑变性的渗出型

Q4 Biochemistry, Genetics and Molecular Biology Journal of Stem Cells Pub Date : 2015-01-01
Daisuke Iejima, Mao Nakayama, Takeshi Iwata
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引用次数: 0

摘要

老年性黄斑变性(AMD)是导致老年人视力下降和失明的主要原因。在美国,干性黄斑变性更为常见,约占黄斑变性患者的 85-90%,而日本的黄斑变性患者则主要发展为湿性黄斑变性或多形性脉络膜血管病(PCV)。最近的研究表明,丝氨酸蛋白酶基因 HTRA1 是湿型 AMD 的主要风险因素(De Wan 等人,Science 2006)。此外,我们还报道了日本典型湿性 AMD 患者与 ARMS2/HTRA1 有显著关联(Goto, Akahori et al.)本研究的目的是阐明湿性 AMD 患者 ARMS2/HTRA1 基因启动子的功能。启动子序列实验显示,大量 AMD 患者的 HTRA1 基因上游 3.8 kb 处存在特异性 indel 突变。与对照序列相比,在HTRA1启动子中观察到启动子活性增加了2-3倍(Iejima等人,JBC 2015)。此外,我们利用鸡作用启动子创建了泛在过表达小鼠 HtrA1 的转基因小鼠,结果表明在体内持续诱导 HtrA1 会导致 CNV,与湿性 AMD 患者类似(Nakayama、Iejima 等人,IOVS 2014)。这些结果表明,人类HTRA1基因启动子区的AMD特异性吲哚突变会增强HTRA1的表达,而这种增强的HTRA1可能与诱导视网膜新生血管有关。
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HTRA1 Overexpression Induces the Exudative Form of Age-related Macular Degeneration.

Age-related macular degeneration (AMD) is a leading cause of vision loss and blindness in the elderly. The dry form is more common and accounts for about 85-90% of AMD patients in US, while Japanese AMD patients predominantly progress to wet-form or polypoidal choroidal vasculopathy (PCV). Recent studies have shown HTRA1, a serine protease gene, as major risk factor for wet form AMD (De Wan et al., Science 2006). Furthermore, we reported that the Japanese typical wet form AMD patients showed significant association with ARMS2/HTRA1 (Goto, Akahori et al., JOBDI 2009). The purpose of this study is to elucidate the function of ARMS2/HTRA1 gene promoter in wet-form AMD patients. The promoter sequence experiment showed that a great number of AMD patients had specific indel mutation in 3.8 kb upstream of HTRA1 gene. 2-3-fold increase of promoter activity was observed in indel HTRA1 promoter compared to control sequence (Iejima et al., JBC 2015). Furthermore, we created transgenic mice ubiquitously overexpressing mouse HtrA1 using the chicken act in promoter, continuous induction of HtrA1 in vivo was shown to lead to CNV, similar to wet AMD patients (Nakayama, Iejima et al., IOVS 2014). These results suggest that human HTRA1 expression is enhanced by AMD specific indel mutation in the promoter region of HTRA1 gene, and this enhanced HTRA1 may be concerned with induce retinal neovasucularization.

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来源期刊
Journal of Stem Cells
Journal of Stem Cells Medicine-Transplantation
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0.10
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1
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