视网膜色素上皮细胞中与年龄和疾病相关的结构变化。
Age and disease-related structural changes in the retinal pigment epithelium.
作者信息
Bonilha Vera L
机构信息
Cole Eye Institute, The Cleveland Clinic, Cleveland, 9500 Euclid Avenue, OH, USA.
出版信息
Clin Ophthalmol. 2008 Jun;2(2):413-24. doi: 10.2147/opth.s2151.
As the retinal pigment epithelium (RPE) ages, a number of structural changes occur, including loss of melanin granules, increase in the density of residual bodies, accumulation of lipofuscin, accumulation of basal deposits on or within Bruch's membrane, formation of drusen (between the basal lamina of the RPE and the inner collagenous layer of Bruch's membrane), thickening of Bruch's membrane, microvilli atrophy and disorganization of the basal infoldings. Although these changes are well known, the basic mechanisms involved in them are frequently poorly understood. These age-related changes progress slowly and vary in severity in different individuals. These changes are also found in age-related macular degeneration (AMD), a late onset disease that severely impacts the RPE, but they are much more pronounced than during normal aging. However, the changes in AMD lead to severe loss of vision. Given the many supporting functions which the RPE serves for the retina, it is important to decipher the age-related changes in this epithelium in order to understand age-related changes in vision.
随着视网膜色素上皮(RPE)老化,会发生许多结构变化,包括黑色素颗粒丢失、残余小体密度增加、脂褐素积累、Bruch膜上或其内部基底沉积物的积累、玻璃膜疣形成(在RPE的基底膜与Bruch膜的内胶原层之间)、Bruch膜增厚、微绒毛萎缩以及基底褶皱紊乱。尽管这些变化广为人知,但其中涉及的基本机制却常常鲜为人知。这些与年龄相关的变化进展缓慢,且在不同个体中的严重程度各异。这些变化在年龄相关性黄斑变性(AMD)中也有发现,AMD是一种严重影响RPE的迟发性疾病,但其变化比正常老化过程中更为明显。然而AMD中的这些变化会导致严重的视力丧失。鉴于RPE为视网膜提供多种支持功能,解读该上皮细胞与年龄相关的变化对于理解与年龄相关的视力变化至关重要。