Takada Y, Uyama M, Ohkuma H, Ogata N, Matsushima M, Deguchi J, Sugasawa K
Department of Ophthalmology, Kansai Medical University, Osaka-fu, Japan.
Nippon Ganka Gakkai Zasshi. 1994 Oct;98(10):955-61.
Age-related macular degeneration is one of the major causes of severe visual loss is elderly individuals. However, relatively little is known about its etiology. The disease may be associated with senescence. Ultrastructural and immunohistochemical studies on SAM (senescence accelerated mouse) eyes were carried out to learn details of aging changes in the retinal pigment epithelium (RPE) and Bruch's membrane. SAM P 1 mice aged 2, 10, 14 months were examined in this study. The eyes were analysed for type IV collagen and heparan sulfate proteoglycan (HSPG) by the avidin-biotin-peroxidase complexes (ABC) method and post-embeddig immunolocalization with colloidal gold. With the ABC method, the basement membranes of both the RPE and the choriocapillaris showed markedly positive staining when treated with anti-type IV collagen antibody and moderately positive staining when treated with anti-HSPG antibody. In ultrastructural immunolocalization, both basement membranes showed fairly heavy labeling in response to the antibodies to type IV collagen, and moderate labeling in response to the antibodies to HSPG. With aging, the thickness of the basement membrane of the choriocapillaris and gold particle labeling by the antibodies to type IV collagen increased. The gold particle labeling by the antibodies to HSPG increased slightly, but was distributed sparsely. These results showed the advancing process of senescence changes in Bruch's membrane.
年龄相关性黄斑变性是老年人严重视力丧失的主要原因之一。然而,对其病因了解相对较少。该疾病可能与衰老有关。对快速老化小鼠(SAM)的眼睛进行了超微结构和免疫组织化学研究,以了解视网膜色素上皮(RPE)和布鲁赫膜衰老变化的细节。本研究检查了2、10、14个月大的SAM P1小鼠。通过抗生物素蛋白-生物素-过氧化物酶复合物(ABC)法以及用胶体金进行包埋后免疫定位,分析眼睛中的IV型胶原和硫酸乙酰肝素蛋白聚糖(HSPG)。采用ABC法,用抗IV型胶原抗体处理时,RPE和脉络膜毛细血管的基底膜均显示出明显的阳性染色,用抗HSPG抗体处理时显示出中度阳性染色。在超微结构免疫定位中,两种基底膜对IV型胶原抗体均显示出相当强的标记,对HSPG抗体显示出中度标记。随着年龄增长,脉络膜毛细血管基底膜的厚度以及IV型胶原抗体的金颗粒标记增加。HSPG抗体的金颗粒标记略有增加,但分布稀疏。这些结果显示了布鲁赫膜衰老变化的进展过程。