Yamada T, Yamanaka I
Department of Neurology, Chiba University, Japan.
Neurosci Lett. 1995 Apr 14;189(2):73-6. doi: 10.1016/0304-3940(95)11452-3.
The localization of the alpha-interferon receptor (alpha-IFNR) was examined in human brain tissues from neurologically normal, Alzheimer's disease (AD) and cerebral infarction cases, using one antibody (IFNaR3) which preferentially recognizes alpha 2-IFN receptor and a second antibody (anti-p40) which recognizes the soluble alpha-IFN alpha/beta receptor. In all cases, microglial cells were stained with the antibodies. In infarct brains, macrophages were intensely labeled for alpha-IFNR. The anti-p40 antibody also showed capillary staining which might be due to residual blood plasma. On Western blots, IFNaR3 recognized only a 210 kDa alpha-IFN/receptor complex, indicating its localization in microglial cells. The anti-p40 antibody recognized this complex as well as four other major materials of lower molecular weight. These results suggest that alpha-IFNR protein is constitutively expressed in microglial cells.
利用一种优先识别α2 - 干扰素受体的抗体(IFNaR3)和另一种识别可溶性α - 干扰素α/β受体的抗体(抗p40),对神经功能正常、患有阿尔茨海默病(AD)和脑梗死病例的人脑组织中的α - 干扰素受体(α - IFNR)进行定位研究。在所有病例中,小胶质细胞均被抗体染色。在梗死脑中,巨噬细胞被α - IFNR强烈标记。抗p40抗体也显示出毛细血管染色,这可能是由于残留血浆所致。在蛋白质免疫印迹分析中,IFNaR3仅识别一种210 kDa的α - 干扰素/受体复合物,表明其定位于小胶质细胞中。抗p40抗体识别该复合物以及其他四种较低分子量的主要物质。这些结果表明,α - IFNR蛋白在小胶质细胞中组成性表达。