Yamada T, Horisberger M A, Kawaguchi N, Moroo I, Toyoda T
Department of Neurology, School of Medicine, Chiba University, Japan.
Neurosci Lett. 1994 Nov 7;181(1-2):61-4. doi: 10.1016/0304-3940(94)90560-6.
The localization of alpha-interferon (alpha-IFN) and its induced protein, MxA, was examined in human brain tissues from neurologically normal, Alzheimer's disease (AD) and Parkinson's disease (PD) cases. In all cases, a few neurons in the superficial cortical layers and microglial cells in the white matter were stained with the antibody to alpha-IFN. In AD brains, white matter microglia were intensely labeled for alpha-IFN and reactive microglia, such as those on senile plaques, were strongly positive for MxA protein. In PD, Lewy bodies in the substantia nigra were positive for MxA, but there was no staining for alpha-IFN in that region. These results suggest that increased expression of alpha-IFN in the white matter microglia and appearance of MxA protein in reactive microglia contribute to Alzheimer pathology. The staining of some Lewy bodies for MxA may be indicative of a viral infection or other unknown factor.
在神经功能正常、患有阿尔茨海默病(AD)和帕金森病(PD)的人类脑组织中,检测了α-干扰素(α-IFN)及其诱导蛋白MxA的定位。在所有病例中,浅层皮质层的一些神经元和白质中的小胶质细胞被α-IFN抗体染色。在AD脑中,白质小胶质细胞被α-IFN强烈标记,而反应性小胶质细胞,如老年斑上的那些细胞,MxA蛋白呈强阳性。在PD中,黑质中的路易小体MxA呈阳性,但该区域没有α-IFN染色。这些结果表明,白质小胶质细胞中α-IFN表达增加以及反应性小胶质细胞中出现MxA蛋白与阿尔茨海默病病理学有关。一些路易小体对MxA的染色可能表明存在病毒感染或其他未知因素。