Golden P L, Pardridge W M
UCLA School of Medicine, Department of Medicine, Los Angeles, CA 90095, USA.
Brain Res. 1999 Feb 20;819(1-2):143-6. doi: 10.1016/s0006-8993(98)01305-5.
Sites of immunoreactive P-glycoprotein associated with human brain microvasculature were identified by labeling of unfixed isolated human brain capillaries, allowing visualization of the three-dimensional capillary structure by confocal microscopy. Capillaries isolated from human autopsy brain were dual-labeled with the MRK16 mouse monoclonal antibody (against human P-glycoprotein) and rabbit polyclonal antisera against the human brain microvascular glucose transporter (GLUT1), or glial fibrillary acidic protein (GFAP) on astrocyte foot processes. MRK16 and GLUT1 dual-labeling showed no signal overlap, identical to the staining pattern observed for dual-labeling with anti-GFAP and anti-GLUT1 antibodies: both GFAP and MRK16 labeling were discrete, discontinuous, and not co-localized with continuous GLUT1 labeling of capillary endothelium. In contrast, complete overlap of MRK16 and GFAP labeling demonstrated P-glycoprotein localization on astrocyte foot process remnants at the abluminal face of the brain microvasculature.
通过对未固定的分离人脑毛细血管进行标记,确定了与人脑微血管相关的免疫反应性P-糖蛋白的位点,从而可以通过共聚焦显微镜观察三维毛细血管结构。从人类尸检大脑中分离出的毛细血管用MRK16小鼠单克隆抗体(抗人P-糖蛋白)和抗人脑微血管葡萄糖转运蛋白(GLUT1)或星形胶质细胞足突上的胶质纤维酸性蛋白(GFAP)的兔多克隆抗血清进行双重标记。MRK16和GLUT1双重标记未显示信号重叠,这与用抗GFAP和抗GLUT1抗体进行双重标记所观察到的染色模式相同:GFAP和MRK16标记都是离散的、不连续的,并且不与毛细血管内皮的连续GLUT1标记共定位。相比之下,MRK16和GFAP标记的完全重叠表明P-糖蛋白定位于脑微血管腔外表面的星形胶质细胞足突残余物上。