Fukumoto H, Asami-Odaka A, Suzuki N, Iwatsubo T
Department of Neuropathology and Neuroscience, Faculty of Pharmaceutical Sciences, University of Tokyo, Japan.
Neurodegeneration. 1996 Mar;5(1):13-7. doi: 10.1006/neur.1996.0002.
To gain insight into the role of microglia in the formation of senile plaques (SP), especially in the generation of the two major molecular species of amyloid beta protein (A beta) with different carboxyl (C)-termini, A beta 40 and A beta 42(43), we conducted double immunolabelling studies on tissue sections from the brains of Alzheimer's disease (AD) and non-demented aged individuals using antibodies to the C-termini of A beta and ferritin, a marker for microglia. All SP were A beta 42(43)-positive in AD as well as in non-demented individuals, only a proportion of which were A beta 40-positive. Both in AD and in non-demented individuals, approximately 2/3 of the A beta 40-positive SP were typical SP with amyloid cores, these being almost invariably associated with microglia. A beta 40-positive, uncored SP were also frequently associated with microglia (mean, 74%), whereas only 24% of A beta 40-negative, uncored SP contained microglia. These results suggest that microglia may play a role in the maturation of SP, especially in the generation of A beta 40.
为深入了解小胶质细胞在老年斑(SP)形成中的作用,尤其是在具有不同羧基(C)末端的两种主要淀粉样β蛋白(Aβ)分子种类Aβ40和Aβ42(43)的生成中的作用,我们使用针对Aβ C末端的抗体和作为小胶质细胞标志物的铁蛋白,对阿尔茨海默病(AD)患者和非痴呆老年人脑切片进行了双重免疫标记研究。在AD患者和非痴呆个体中,所有SP均为Aβ42(43)阳性,其中只有一部分为Aβ40阳性。在AD患者和非痴呆个体中,约2/3的Aβ40阳性SP是具有淀粉样核心的典型SP,这些几乎总是与小胶质细胞相关。Aβ40阳性、无核心的SP也经常与小胶质细胞相关(平均为74%),而只有24%的Aβ40阴性、无核心的SP含有小胶质细胞。这些结果表明,小胶质细胞可能在SP的成熟中起作用,尤其是在Aβ40的生成中。