Allsop D, Haga S I, Haga C, Ikeda S I, Mann D M, Ishii T
Psychiatric Research Institute of Tokyo, Department of Molecular Biology, Japan.
Neuropathol Appl Neurobiol. 1989 Nov-Dec;15(6):531-42. doi: 10.1111/j.1365-2990.1989.tb01252.x.
A sensitive methenamine silver/Nissl stain was used to study the morphology and relationship of pre-plaques (presumed early senile plaques) in Down's syndrome brains to glial nuclei, capillaries and neuronal perikarya. The larger pre-plaques (greater than 50 microns) usually encompassed all of these tissue elements. However, the smaller pre-plaques (less than or equal to 50 microns) were almost always found immediately adjacent to, or around the cell bodies of neurons (often with associated satellite cells), and they failed to show any consistent, close spatial relationship to the other tissue components. Thus we consider an early stage of pre-plaque formation to be the deposition of amyloid adjacent to the cell body of a morphologically normal neuron. Based on the study of transitional forms, we suggest that the amyloid progressively accumulates around the cell body until the enclosed neuron degenerates. How these pre-plaque lesions might eventually develop into the typical plaque structure is uncertain. Our observations support the theory of a neuronal origin for plaque amyloid.
采用一种灵敏的六胺银/尼氏染色法,研究唐氏综合征患者大脑中前斑块(推测为早期老年斑)与神经胶质细胞核、毛细血管和神经元胞体的形态及关系。较大的前斑块(大于50微米)通常包含所有这些组织成分。然而,较小的前斑块(小于或等于50微米)几乎总是紧邻神经元胞体或位于其周围(常伴有卫星细胞),且它们与其他组织成分未显示出任何一致、紧密的空间关系。因此,我们认为前斑块形成的早期阶段是淀粉样蛋白在形态正常的神经元胞体附近沉积。基于对过渡形式的研究,我们认为淀粉样蛋白逐渐在胞体周围积聚,直至被包裹的神经元退化。这些前斑块病变最终如何发展为典型的斑块结构尚不确定。我们的观察结果支持斑块淀粉样蛋白起源于神经元的理论。