探讨ARMS2和HTRA1基因在老年性黄斑变性中的作用。

IF 18.6 1区 医学 Q1 OPHTHALMOLOGY
Yang Pan , Yingbin Fu , Paul N. Baird , Robyn H. Guymer , Taraprasad Das , Takeshi Iwata
{"title":"探讨ARMS2和HTRA1基因在老年性黄斑变性中的作用。","authors":"Yang Pan ,&nbsp;Yingbin Fu ,&nbsp;Paul N. Baird ,&nbsp;Robyn H. Guymer ,&nbsp;Taraprasad Das ,&nbsp;Takeshi Iwata","doi":"10.1016/j.preteyeres.2022.101159","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>Age-related macular degeneration (AMD) is the leading cause of severe irreversible central vision loss in individuals over 65 years old. Genome-wide association studies (GWASs) have shown that the region at chromosome 10q26, where the age-related </span>maculopathy susceptibility (</span><em>ARMS2/LOC387715</em><span>) and HtrA serine peptidase 1 (</span><em>HTRA1</em>) genes are located, represents one of the strongest associated loci for AMD. However, the underlying biological mechanism of this genetic association has remained elusive. In this article, we extensively review the literature by us and others regarding the <em>ARMS2/HTRA1</em><span><span><span> risk alleles and their functional significance. We also review the literature regarding the presumed function of the ARMS2 protein and the molecular processes<span> of the HTRA1 protein in AMD pathogenesis in vitro and in vivo, including those of transgenic mice overexpressing HtrA1/HTRA1 which developed </span></span>Bruch's membrane (BM) damage, </span>choroidal neovascularization<span> (CNV), and polypoidal choroidal vasculopathy (PCV), similar to human AMD patients. The elucidation of the molecular mechanisms of the </span></span><em>ARMS2</em> and <em>HTRA1</em><span><span> susceptibility loci has begun to untangle the complex biological pathways underlying AMD pathophysiology, pointing to new testable paradigms for </span>treatment.</span></p></div>","PeriodicalId":21159,"journal":{"name":"Progress in Retinal and Eye Research","volume":null,"pages":null},"PeriodicalIF":18.6000,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":"{\"title\":\"Exploring the contribution of ARMS2 and HTRA1 genetic risk factors in age-related macular degeneration\",\"authors\":\"Yang Pan ,&nbsp;Yingbin Fu ,&nbsp;Paul N. Baird ,&nbsp;Robyn H. Guymer ,&nbsp;Taraprasad Das ,&nbsp;Takeshi Iwata\",\"doi\":\"10.1016/j.preteyeres.2022.101159\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span><span>Age-related macular degeneration (AMD) is the leading cause of severe irreversible central vision loss in individuals over 65 years old. Genome-wide association studies (GWASs) have shown that the region at chromosome 10q26, where the age-related </span>maculopathy susceptibility (</span><em>ARMS2/LOC387715</em><span>) and HtrA serine peptidase 1 (</span><em>HTRA1</em>) genes are located, represents one of the strongest associated loci for AMD. However, the underlying biological mechanism of this genetic association has remained elusive. In this article, we extensively review the literature by us and others regarding the <em>ARMS2/HTRA1</em><span><span><span> risk alleles and their functional significance. We also review the literature regarding the presumed function of the ARMS2 protein and the molecular processes<span> of the HTRA1 protein in AMD pathogenesis in vitro and in vivo, including those of transgenic mice overexpressing HtrA1/HTRA1 which developed </span></span>Bruch's membrane (BM) damage, </span>choroidal neovascularization<span> (CNV), and polypoidal choroidal vasculopathy (PCV), similar to human AMD patients. The elucidation of the molecular mechanisms of the </span></span><em>ARMS2</em> and <em>HTRA1</em><span><span> susceptibility loci has begun to untangle the complex biological pathways underlying AMD pathophysiology, pointing to new testable paradigms for </span>treatment.</span></p></div>\",\"PeriodicalId\":21159,\"journal\":{\"name\":\"Progress in Retinal and Eye Research\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":18.6000,\"publicationDate\":\"2023-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Progress in Retinal and Eye Research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1350946222001197\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"OPHTHALMOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Progress in Retinal and Eye Research","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1350946222001197","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"OPHTHALMOLOGY","Score":null,"Total":0}
引用次数: 4

摘要

年龄相关性黄斑变性(AMD)是65岁以上人群严重不可逆中心视力丧失的主要原因。全基因组关联研究(GWASs)表明,年龄相关性黄斑病变易感性(ARMS2/LOC387715)和HtrA丝氨酸肽酶1(HTRA1)基因所在的染色体10q26区域是AMD最强的关联基因座之一。然而,这种基因关联的潜在生物学机制仍然难以捉摸。在这篇文章中,我们广泛回顾了我们和其他人关于ARMS2/HTRA1风险等位基因及其功能意义的文献。我们还回顾了关于ARMS2蛋白的假定功能和HTRA1蛋白在体外和体内AMD发病机制中的分子过程的文献,包括过表达HTRA1/HTRA1的转基因小鼠的文献,这些小鼠与人类AMD患者类似,产生布鲁赫膜(BM)损伤、脉络膜新生血管(CNV)和息肉状脉络膜血管病(PCV)。ARMS2和HTRA1易感基因座的分子机制的阐明已经开始解开AMD病理生理学的复杂生物学途径,为治疗提供了新的可测试的范例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring the contribution of ARMS2 and HTRA1 genetic risk factors in age-related macular degeneration

Age-related macular degeneration (AMD) is the leading cause of severe irreversible central vision loss in individuals over 65 years old. Genome-wide association studies (GWASs) have shown that the region at chromosome 10q26, where the age-related maculopathy susceptibility (ARMS2/LOC387715) and HtrA serine peptidase 1 (HTRA1) genes are located, represents one of the strongest associated loci for AMD. However, the underlying biological mechanism of this genetic association has remained elusive. In this article, we extensively review the literature by us and others regarding the ARMS2/HTRA1 risk alleles and their functional significance. We also review the literature regarding the presumed function of the ARMS2 protein and the molecular processes of the HTRA1 protein in AMD pathogenesis in vitro and in vivo, including those of transgenic mice overexpressing HtrA1/HTRA1 which developed Bruch's membrane (BM) damage, choroidal neovascularization (CNV), and polypoidal choroidal vasculopathy (PCV), similar to human AMD patients. The elucidation of the molecular mechanisms of the ARMS2 and HTRA1 susceptibility loci has begun to untangle the complex biological pathways underlying AMD pathophysiology, pointing to new testable paradigms for treatment.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
34.10
自引率
5.10%
发文量
78
期刊介绍: Progress in Retinal and Eye Research is a Reviews-only journal. By invitation, leading experts write on basic and clinical aspects of the eye in a style appealing to molecular biologists, neuroscientists and physiologists, as well as to vision researchers and ophthalmologists. The journal covers all aspects of eye research, including topics pertaining to the retina and pigment epithelial layer, cornea, tears, lacrimal glands, aqueous humour, iris, ciliary body, trabeculum, lens, vitreous humour and diseases such as dry-eye, inflammation, keratoconus, corneal dystrophy, glaucoma and cataract.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信