Department of Neuroscience, Pharmacogly, University of Uppsala, The Biomedical Center Husargatan 3, Box 593, 751 23, Uppsala, Sweden.
Department of Medical Cell Biology, University of Uppsala, The Biomedical Center Husargatan 3, Box 571, 751 23, Uppsala, Sweden.
Acta Neuropathol Commun. 2021 May 10;9(1):84. doi: 10.1186/s40478-021-01182-x.
Defective amyloid-β (Aβ) clearance from the brain is a major contributing factor to the pathophysiology of Alzheimer's disease (AD). Aβ clearance is mediated by macrophages, enzymatic degradation, perivascular drainage along the vascular basement membrane (VBM) and transcytosis across the blood-brain barrier (BBB). AD pathology is typically associated with cerebral amyloid angiopathy due to perivascular accumulation of Aβ. Heparan sulfate (HS) is an important component of the VBM, thought to fulfill multiple roles in AD pathology. We previously showed that macrophage-mediated clearance of intracortically injected Aβ was impaired in the brains of transgenic mice overexpressing heparanase (Hpa-tg). This study revealed that perivascular drainage was impeded in the Hpa-tg brain, evidenced by perivascular accumulation of the injected Aβ in the thalamus of Hpa-tg mice. Furthermore, endogenous Aβ accumulated at the perivasculature of Hpa-tg thalamus, but not in control thalamus. This perivascular clearance defect was confirmed following intracortical injection of dextran that was largely retained in the perivasculature of Hpa-tg brains, compared to control brains. Hpa-tg brains presented with thicker VBMs and swollen perivascular astrocyte endfeet, as well as elevated expression of the BBB-associated water-pump protein aquaporin 4 (AQP4). Elevated levels of both heparanase and AQP4 were also detected in human AD brain. These findings indicate that elevated heparanase levels alter the organization and composition of the BBB, likely through increased fragmentation of BBB-associated HS, resulting in defective perivascular drainage. This defect contributes to perivascular accumulation of Aβ in the Hpa-tg brain, highlighting a potential role for heparanase in the pathogenesis of AD.
脑内淀粉样蛋白-β(Aβ)清除功能缺陷是阿尔茨海默病(AD)病理生理学的主要致病因素。Aβ的清除由巨噬细胞介导,通过酶降解、沿血管基底膜(VBM)的血管周围引流和血脑屏障(BBB)的跨细胞转运来实现。AD 病理通常与血管周围 Aβ积累相关的脑淀粉样血管病有关。硫酸乙酰肝素(HS)是 VBM 的重要组成部分,被认为在 AD 病理中具有多种作用。我们之前的研究表明,过表达乙酰肝素酶(Hpa-tg)的转基因小鼠脑内注射的 Aβ的巨噬细胞介导清除受到损害。这项研究表明,Hpa-tg 脑内的血管周围引流受到阻碍,证据是 Hpa-tg 小鼠丘脑内注射的 Aβ在血管周围积累。此外,内源性 Aβ在 Hpa-tg 丘脑的血管周围堆积,但在对照丘脑没有。在 Hpa-tg 脑内,与对照脑相比,经皮质内注射的葡聚糖大部分保留在血管周围,证实了这种血管周围清除缺陷。Hpa-tg 脑表现出较厚的 VBM 和肿胀的血管周围星形细胞足突,以及血脑屏障相关水泵蛋白 aquaporin 4(AQP4)的表达升高。人类 AD 脑中也检测到乙酰肝素酶和 AQP4 的水平升高。这些发现表明,升高的乙酰肝素酶水平改变了 BBB 的组织和组成,可能是通过增加 BBB 相关 HS 的片段化,导致血管周围引流功能缺陷。这种缺陷导致 Hpa-tg 脑内 Aβ在血管周围的积累,突出了乙酰肝素酶在 AD 发病机制中的潜在作用。