Mufson E J, Kordower J H
Department of Neurological Sciences, Rush Presbyterian/St. Luke's Medical Center, Chicago, IL 60612.
Proc Natl Acad Sci U S A. 1992 Jan 15;89(2):569-73. doi: 10.1073/pnas.89.2.569.
Using a monoclonal antibody directed against the primate nerve growth factor (NGF) receptor, we examined the expression of NGF receptors within neuronal perikarya of normal adult human cerebral cortex (27-98 years old) and individuals with Alzheimer disease (AD). This expression of cortical NGF receptors was compared with that seen in other neurological diseases and normal human development as well as in young and aged nonhuman primates. NGF receptor-containing cortical neurons were not observed in young adults (less than 50 years old) and were observed only infrequently in non-demented elderly individuals (50-80 years old). In contrast, numerous NGF receptor-containing cortical neurons were seen in AD patients of all ages and in one 98-year-old nondemented patient. In advanced age and AD, numerous NGF receptor-positive neurons were located within laminae II-VI of temporal association cortices whereas only a few were seen in the subicular complex, entorhinal cortex, parahippocampal gyrus, and amygdaloid complex. These perikarya appeared healthy, with bipolar, fusiform, or multipolar morphologies and extended varicose dendritic arbors. These neurons failed to express neurofibrillary tangle-bearing material. In contrast to AD, NGF receptor-containing cortical neurons were not observed in Parkinson disease, Pick disease, or Shy-Drager syndrome. The NGF receptor-containing cortical neurons seen in advanced age and AD were similar in morphology to those observed in human fetal cortex. No NGF receptor-containing cortical neurons were observed in young or aged nonhuman primates. These findings suggest that neurons within the human cerebral cortex exhibit plasticity in their expression of NGF receptors in AD and extreme advanced aging.
我们使用一种针对灵长类神经生长因子(NGF)受体的单克隆抗体,检测了正常成人大脑皮质(27 - 98岁)以及阿尔茨海默病(AD)患者神经元胞体中NGF受体的表达情况。将皮质NGF受体的这种表达与其他神经系统疾病、正常人类发育以及年轻和老年非人灵长类动物中的情况进行了比较。在年轻成年人(小于50岁)中未观察到含有NGF受体的皮质神经元,在非痴呆老年人(50 - 80岁)中也仅偶尔观察到。相比之下,在各年龄段的AD患者以及一名98岁的非痴呆患者中均可见大量含有NGF受体的皮质神经元。在高龄和AD患者中,大量NGF受体阳性神经元位于颞叶联合皮质的II - VI层,而在海马下复合体、内嗅皮质、海马旁回和杏仁复合体中仅见少数。这些胞体看起来健康,具有双极、梭形或多极形态,并延伸出曲张的树突分支。这些神经元未表达含有神经原纤维缠结的物质。与AD不同,在帕金森病、皮克病或夏伊 - 德雷格综合征中未观察到含有NGF受体的皮质神经元。在高龄和AD患者中看到的含有NGF受体的皮质神经元在形态上与人类胎儿皮质中观察到的相似。在年轻或老年非人灵长类动物中未观察到含有NGF受体的皮质神经元。这些发现表明,人类大脑皮质中的神经元在AD和极端高龄时其NGF受体表达具有可塑性。