首页> 美国卫生研究院文献>The British Journal of Ophthalmology >Early stages of age-related macular degeneration: an immunofluorescence and electron microscopy study.
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Early stages of age-related macular degeneration: an immunofluorescence and electron microscopy study.

机译:年龄相关性黄斑变性的早期阶段:免疫荧光和电子显微镜研究。

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摘要

In subretinal neovascularisation capillaries originating from the choriocapillaris must cross Bruch's membrane to reach the subretinal pigment epithelial space. Thus gaps in Bruch's membrane have to be formed before subretinal neovascularisation. Histological examination of eyes with subretinal neovascularisation or disciform scars has shown macrophages adjacent to thin areas and ruptures in Bruch's membrane. This has been interpreted as phagocytosis of Bruch's membrane. The purpose of this study was to investigate whether immune complex depositions can be detected in maculae with early stages of age-related macular degeneration and to explain the macrophage reaction before the disciform reaction. A series of 20 human maculae were examined by direct immunofluorescence light microscopy to detect the presence of immune complexes with antibodies directed against immunoglobulins, fibrinogen, and complement factors. Transmission electron microscopy on several maculae was performed to identify the macrophages. Macrophages were observed in close relation to the readily recognisable long spacing collagen, which suggested that long spacing collagen was selectively internalised by these cells. Definite immune complex depositions were not found in basal laminar deposits or drusen. Linear deposits of fibrinogen and complement were frequently found in the outer collagenous zone of Bruch's membrane. However, because of the absence of immunoglobulins, it seems unlikely that these non-specific deposits might cause chemoattraction of macrophages and play a role in the initial phase of the development of subretinal neovascularisation and disciform macular degeneration.
机译:在视网膜下新生血管形成中,源自脉络膜毛细血管的毛细血管必须穿过Bruch膜才能到达视网膜下色素上皮空间。因此,必须在视网膜下新生血管形成之前在布鲁赫膜上形成间隙。对具有视网膜下新血管形成或盘状疤痕的眼睛进行的组织学检查显示,巨噬细胞邻近薄区域,布鲁赫膜破裂。这已被解释为布鲁赫膜的吞噬作用。这项研究的目的是调查是否可以在年龄相关性黄斑变性的早期阶段在黄斑中检测到免疫复合物沉积,并解释盘状反应之前的巨噬细胞反应。通过直接免疫荧光显微镜检查了一系列20个人类黄斑,以检测针对免疫球蛋白,纤维蛋白原和补体因子的抗体是否存在免疫复合物。在几个黄斑上进行透射电子显微镜以鉴定巨噬细胞。观察到巨噬细胞与易于识别的长间距胶原紧密相关,这表明长间距胶原被这些细胞选择性地内在化。在基底层沉积或玻璃疣中未发现明确的免疫复合物沉积。纤维蛋白原和补体的线性沉积物经常在布鲁赫膜的外胶原区中发现。但是,由于缺乏免疫球蛋白,这些非特异性沉积物似乎不太可能引起巨噬细胞的化学引诱,并在视网膜下新血管形成和盘状黄斑变性的发展的初始阶段发挥作用。

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