Kimchi E Y, Kajdasz S, Bacskai B J, Hyman B T
Department of Neurology, Massachusetts General Hospital, Charlestown 02129, USA.
J Neuropathol Exp Neurol. 2001 Mar;60(3):274-9. doi: 10.1093/jnen/60.3.274.
Transgenic mice overexpressing the human amyloid precursor protein (APPV717F) develop cerebral amyloid angiopathy (CAA) as they age. We have examined the effect of CAA on blood vessels in vivo using multiphoton laser scanning microscopy. We are able to simultaneously detect, in an alive but anesthetized animal, fluorescent angiography of microvessels as well as the presence of amyloid angiopathy in 3-dimensional volumes near the surface of the brain. Analysis revealed dilation of the portions of vessels that were associated with amyloid deposition, even when that amyloid deposition was quite mild. In addition, analysis of the 3-dimensional reconstruction of the relationship between the vasculature and CAA suggest that CAA is initiated close to branch points of vessels. Taken together, these data suggest that CAA has a substantial effect on the physiology of the microvasculature in vivo.
随着年龄增长,过度表达人类淀粉样前体蛋白(APPV717F)的转基因小鼠会出现脑淀粉样血管病(CAA)。我们使用多光子激光扫描显微镜检查了CAA在体内对血管的影响。我们能够在一只活着但已麻醉的动物体内同时检测微血管的荧光血管造影以及脑表面附近三维体积内淀粉样血管病的存在。分析显示,即使淀粉样沉积相当轻微,与淀粉样沉积相关的血管部分也会扩张。此外,对脉管系统与CAA之间关系的三维重建分析表明,CAA在血管分支点附近开始形成。综上所述,这些数据表明CAA对体内微血管的生理功能有重大影响。