Katschke Kenneth J, Truong Tom, Pham Victoria, Xi Hongkang, Tang Wanjian, Gu Xiaowu, Teotia Pooja, Hofmann Jeffrey W, Chaney Shawnta Y, Kirchhofer Daniel, van Lookeren Campagne Menno, Jeanne Marion
Department of Immunology, Genentech Inc., South San Francisco, CA 94080, USA.
Department of Translational Immunology, Genentech Inc., South San Francisco, CA 94080, USA.
Dis Model Mech. 2025 Oct 1;18(10). doi: 10.1242/dmm.052253. Epub 2025 Sep 17.
Polymorphisms in the ARMS2/HTRA1 locus on chromosome 10 enhance the risk of geographic atrophy and macular neovascularization, the advanced forms of age-related macular degeneration (AMD). Although HTRA1 mutations have been associated with microvascular defects in the brain, it remains unclear whether changes in HTRA1 expression contribute to AMD pathophysiology. In this study, we showed that, in AMD donor eyes, HTRA1 protein accumulated around the retinal pigment epithelium (RPE)/photoreceptor lesions. We then demonstrated that overexpression of catalytically active, but not catalytically inactive, HTRA1 in RPE cells in mice induced age-dependent loss of photoreceptors, inflammation and a decline in photoreceptor functional responses. This retinal degeneration was not exacerbated when the mice were exposed to phototoxic stress in the constant light exposure preclinical model. However, mice overexpressing catalytically active HTRA1 had significant exacerbation of laser-induced choroidal neovascularization lesions. Finally, as substrate processing may define the molecular basis for HTRA1-induced retinal degeneration, we initiated a proteomics approach and identified the visual cycle key player RBP3 as a disease-relevant HTRA1 substrate in the retina.
位于10号染色体上的ARMS2/HTRA1基因座的多态性会增加地图样萎缩和黄斑新生血管形成的风险,这两种情况是年龄相关性黄斑变性(AMD)的晚期形式。尽管HTRA1突变与脑部微血管缺陷有关,但HTRA1表达的变化是否导致AMD的病理生理过程仍不清楚。在本研究中,我们发现,在AMD供体眼中,HTRA1蛋白在视网膜色素上皮(RPE)/光感受器病变周围积聚。然后我们证明,在小鼠的RPE细胞中过表达具有催化活性而非无催化活性的HTRA1会导致光感受器出现年龄依赖性丧失、炎症以及光感受器功能反应下降。在持续光照临床前模型中,当小鼠暴露于光毒性应激时,这种视网膜变性并未加剧。然而,过表达具有催化活性HTRA1的小鼠激光诱导的脉络膜新生血管病变显著加重。最后,由于底物加工可能决定HTRA1诱导视网膜变性的分子基础,我们启动了蛋白质组学方法,并确定视觉循环关键因子RBP3是视网膜中与疾病相关的HTRA1底物。