Kuo H, Ingram D K, Walker L C, Tian M, Hengemihle J M, Jucker M
Nathan W. shock Laboratories, National Institute on Aging, NIH, Baltimore, MD 21224, USA.
Neuroscience. 1996 Oct;74(3):733-40. doi: 10.1016/0306-4522(96)00169-8.
With advancing age clusters of abnormal granules positive for periodic acid-Schiff appear in the hippocampus of C57BL/6 (B6) mice and the senescence-accelerated mouse (SAM) P8. The granules can also be visualized with a polyclonal antibody to a 110,000 mol. wt laminin-binding protein and stain specifically with a monoclonal antibody to heparan sulfate proteoglycan. The present study used light and electron-microscopic analysis to compare the staining and morphological properties of these granules in SAM P8 hippocampus with those in B6 hippocampus at different ages. The results of the light-microscopic analysis revealed that granules in SAM P8 and B6 had similar morphology, staining characteristics and distribution patterns, and appeared to have a close association with astrocytic process. The onset of granules in SAM P8 mice (at two to three months of age) was earlier than that observed in B6 mice (at four to six months of age), but the maximum incidence was similar in both strains. Electron-microscopic analysis revealed that the granules in SAM P8 and B6 mice also had a very similar ultrastructure. Granules in both strains were surrounded by a discontinuous membrane and contained mostly crystalline-like, degenerated material. The successive ultrastructural changes from the exterior to interior of the granules suggest that the degenerative process was initiated outside the granules and that degenerative structures migrate inward. Astrocytes and heparan sulfate proteoglycan are closely associated with beta-amyloid deposits in Alzheimer's disease. The presence of astrocyte-associated heparan sulfate proteoglycan-positive material in aged SAM P8 and B6 mice might model age-related alterations in glia function possibly involved in human cerebral amyloidogenesis.
随着年龄的增长,在C57BL/6(B6)小鼠和衰老加速小鼠(SAM)P8的海马体中出现了对高碘酸 - 希夫反应呈阳性的异常颗粒簇。这些颗粒也可用针对110,000摩尔分子量层粘连蛋白结合蛋白的多克隆抗体进行可视化,并能用针对硫酸乙酰肝素蛋白聚糖的单克隆抗体进行特异性染色。本研究采用光镜和电镜分析,比较了不同年龄的SAM P8海马体和B6海马体中这些颗粒的染色和形态学特性。光镜分析结果显示,SAM P8和B6中的颗粒具有相似的形态、染色特征和分布模式,并且似乎与星形胶质细胞突起密切相关。SAM P8小鼠(2至3个月龄)中颗粒的出现早于B6小鼠(4至6个月龄),但两种品系的最大发生率相似。电镜分析显示,SAM P8和B6小鼠中的颗粒也具有非常相似的超微结构。两种品系中的颗粒都被不连续的膜包围,并且主要包含类晶体状的退化物质。颗粒从外部到内部的连续超微结构变化表明,退化过程在颗粒外部开始,并且退化结构向内迁移。在阿尔茨海默病中,星形胶质细胞和硫酸乙酰肝素蛋白聚糖与β-淀粉样蛋白沉积密切相关。老年SAM P8和B6小鼠中存在与星形胶质细胞相关的硫酸乙酰肝素蛋白聚糖阳性物质,可能模拟了可能参与人类脑淀粉样蛋白生成的神经胶质细胞功能的年龄相关变化。