Leveugle B, Fillit H
Department of Geriatrics and Adult Development, Mount Sinai Medical Center, New York, NY 10029.
Mol Neurobiol. 1994 Aug-Dec;9(1-3):25-32. doi: 10.1007/BF02816102.
Alzheimer's disease is a dementing disorder affecting increasingly large numbers of individuals in the aging population. The characteristic neuropathologic changes of Alzheimer's disease are the deposition of extracellular amyloid plaques, neurons containing neurofibrillary tangles, and neuronal cell loss. The A4 amyloid peptide is the major constituent of senile plaques. In addition to the A4 peptide, senile plaques contain a variety of molecular species, including proteoglycans and inflammatory components. The presence of proteoglycans in the amyloid deposits of Alzheimer's disease and of systemic amyloidoses suggests that these molecules play an active role in the pathogenesis of amyloidosis. However, the molecular mechanisms that lead to the codeposition of amyloid peptide with proteoglycans is still unknown. Recent evidence suggests that the metabolism of proteoglycans is altered in Alzheimer's disease patients. The acute-phase response observed in the brain of patients affected by Alzheimer's disease may be responsible for this effect. In this article, we discuss the role of proteoglycans in Alzheimer's disease, and the possible interactions between factors involved in brain inflammatory mechanisms and proteoglycans in the pathogenesis of Alzheimer's disease.
阿尔茨海默病是一种痴呆症,影响着老年人口中越来越多的个体。阿尔茨海默病的典型神经病理变化是细胞外淀粉样斑块的沉积、含有神经原纤维缠结的神经元以及神经元细胞丢失。A4淀粉样肽是老年斑的主要成分。除了A4肽,老年斑还含有多种分子成分,包括蛋白聚糖和炎症成分。蛋白聚糖在阿尔茨海默病和系统性淀粉样变性的淀粉样沉积物中的存在表明这些分子在淀粉样变性的发病机制中起积极作用。然而,导致淀粉样肽与蛋白聚糖共沉积的分子机制仍然未知。最近的证据表明,阿尔茨海默病患者体内蛋白聚糖的代谢发生了改变。在受阿尔茨海默病影响的患者大脑中观察到的急性期反应可能是造成这种影响的原因。在本文中,我们讨论了蛋白聚糖在阿尔茨海默病中的作用,以及参与脑部炎症机制的因素与蛋白聚糖在阿尔茨海默病发病机制中可能存在的相互作用。