Blasiak Janusz, Salminen Antero, Kaarniranta Kai
Department of Molecular Genetics, University of Lodz, Lodz, Poland.
Front Biosci (Schol Ed). 2013 Jan 1;5(2):412-25. doi: 10.2741/s380.
Age-related macular degeneration (AMD) is an ocular disease and the main reason for sight loss in the elderly in the developed countries. The pathogenesis of the disease is complex and not fully understood, but involves several environmental and genetic risk factors. However, little is known about the role of epigenetics in this disease although it is recognized that epigenetic alterations often precede genetic changes in many pathological conditions and regulate aging and the developmental processes. There is experimental evidence for the involvement of DNA methylation and histone modifications in the pathogenesis of drusen formation, a central hallmark of AMD. However, the main impact of epigenetic modifications, including persistent lysine methylation of the H3 histone, is exerted during retinal embryonic development. This interplay opens an exciting possibility to manipulate the epigenetic pattern and to develop novel AMD therapies by physical, pharmacological or genetic interventions. One of the most intriguing questions is why different individuals develop different AMD phenotypes. Epigenetic regulation might open new perspectives into these changes in AMD pathology.
年龄相关性黄斑变性(AMD)是一种眼部疾病,是发达国家老年人视力丧失的主要原因。该疾病的发病机制复杂,尚未完全明确,但涉及多种环境和遗传风险因素。然而,尽管人们认识到表观遗传学改变在许多病理状况下常常先于基因变化并调节衰老及发育过程,但对于表观遗传学在这种疾病中的作用却知之甚少。有实验证据表明DNA甲基化和组蛋白修饰参与了玻璃膜疣形成的发病机制,玻璃膜疣是AMD的一个核心特征。然而,表观遗传修饰的主要影响,包括H3组蛋白的持续赖氨酸甲基化,是在视网膜胚胎发育过程中发挥作用的。这种相互作用为通过物理、药理学或基因干预来操纵表观遗传模式并开发新型AMD疗法提供了令人兴奋的可能性。最引人入胜的问题之一是为什么不同个体发展出不同的AMD表型。表观遗传调控可能为AMD病理学中的这些变化开辟新的视角。