Heise Erich A, Fort Patrice E
Kellogg Eye Center, Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI USA.
J Ocul Biol Dis Infor. 2011 Jun;4(1-2):62-9. doi: 10.1007/s12177-011-9073-7. Epub 2011 Dec 23.
Diabetes and its related complications represent a major growing health concern and economic burden worldwide. Ocular manifestations of diabetes include cataractogenesis and retinopathy, the latter being the leading cause of blindness in the working-age population. Despite numerous studies and recent progress, the exact pathophysiology of the disease remains to be fully elucidated and development of new and improved therapeutic strategies for this chronic condition are greatly needed. Heat shock proteins (Hsps) are highly conserved families of proteins, which are generally regarded as protective molecules that play a wide variety of roles and can be expressed in response to different types of cellular stresses. In recent years, numerous studies have reported their implication in various ocular diseases including diabetic retinopathy. The present review focuses on the potential implication of Hsps in ocular diabetic complications and discusses their specific mechanisms of regulation with respect to their expression, functions and alteration during diabetes. The review will conclude by examining the potential of Hsps as therapeutic agents or targets for the treatment of diabetic retinopathy.
糖尿病及其相关并发症是全球范围内日益严重的主要健康问题和经济负担。糖尿病的眼部表现包括白内障形成和视网膜病变,后者是劳动年龄人口失明的主要原因。尽管进行了大量研究并取得了近期进展,但该疾病的确切病理生理学仍有待充分阐明,因此迫切需要开发针对这种慢性病的新的和改进的治疗策略。热休克蛋白(Hsps)是高度保守的蛋白质家族,通常被视为具有多种作用的保护分子,可在对不同类型的细胞应激作出反应时表达。近年来,大量研究报告了它们在包括糖尿病性视网膜病变在内的各种眼部疾病中的作用。本综述重点关注热休克蛋白在糖尿病眼部并发症中的潜在作用,并讨论它们在糖尿病期间的表达、功能和改变方面的具体调节机制。综述将通过研究热休克蛋白作为治疗糖尿病性视网膜病变的治疗剂或靶点的潜力来得出结论。