Rebeck G W, Harr S D, Strickland D K, Hyman B T
Department of Neurology, Masschusetts General Hospital, Boston 02114.
Ann Neurol. 1995 Feb;37(2):211-7. doi: 10.1002/ana.410370212.
Both apolipoprotein E and its receptor, the low-density-lipoprotein receptor-related protein (LRP), are associated with senile plaques in Alzheimer's disease. We examined the relationship of other LRP-related molecules to senile plaques. LRP is a multifunctional receptor that binds and rapidly internalizes at least seven ligands: apolipoprotein E, activated alpha 2-macroglobulin, tissue and urokinase-type plasminogen activators, plasminogen activator inhibitor-1, lipoprotein lipase, and lactoferrin. Using immunohistochemistry, we showed that all of these ligands, representing a diverse group of otherwise apparently unrelated proteins, accumulate on senile plaques. We also studied expression of the receptor-associated protein, a physiological inhibitor of LRP, in the hippocampal formation from normal subjects and Alzheimer's disease patients. Receptor-associated protein colocalizes with LRP on neuronal soma, but not on neuronal processes or reactive astrocytes. It is not present on senile plaques. These results suggest that senile plaque-associated LRP can bind its ligands, but clearance of these compounds may be impaired in the vicinity of senile plaques.
载脂蛋白E及其受体——低密度脂蛋白受体相关蛋白(LRP)均与阿尔茨海默病中的老年斑有关。我们研究了其他与LRP相关的分子与老年斑的关系。LRP是一种多功能受体,它能结合并快速内化至少七种配体:载脂蛋白E、活化的α2-巨球蛋白、组织型和尿激酶型纤溶酶原激活剂、纤溶酶原激活剂抑制剂-1、脂蛋白脂肪酶和乳铁蛋白。通过免疫组织化学方法,我们发现所有这些配体,它们代表了一组原本看似不相关的不同蛋白质,都在老年斑上积聚。我们还研究了受体相关蛋白(LRP的一种生理抑制剂)在正常受试者和阿尔茨海默病患者海马结构中的表达。受体相关蛋白与LRP在神经元胞体上共定位,但不在神经突或反应性星形胶质细胞上。它不存在于老年斑上。这些结果表明,与老年斑相关的LRP能够结合其配体,但在老年斑附近这些化合物的清除可能受损。