周细胞
神经退行性变
小动脉
脑淀粉样血管病
认知功能衰退
收缩
阿尔茨海默病
神经科学
生物
人脑
微循环
细胞生物学
疾病
病理
化学
医学
内分泌学
内科学
体外
生物化学
内皮干细胞
痴呆
作者
Ross Nortley,Nils Korte,Pablo Izquierdo,Chanawee Hirunpattarasilp,Anusha Mishra,Zane Jaunmuktane,Vasiliki Kyrargyri,Thomas Pfeiffer,Lila Khennouf,Christian Madry,Hui Gong,Angela Richard-Loendt,Wenhui Huang,Takashi Saito,Takaomi C. Saido,Sebastian Brandner,Huma Sethi,David Attwell
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2019-06-20
卷期号:365 (6450)
被引量:676
标识
DOI:10.1126/science.aav9518
摘要
Cerebral blood flow is reduced early in the onset of Alzheimer's disease (AD). Because most of the vascular resistance within the brain is in capillaries, this could reflect dysfunction of contractile pericytes on capillary walls. We used live and rapidly fixed biopsied human tissue to establish disease relevance, and rodent experiments to define mechanism. We found that in humans with cognitive decline, amyloid β (Aβ) constricts brain capillaries at pericyte locations. This was caused by Aβ generating reactive oxygen species, which evoked the release of endothelin-1 (ET) that activated pericyte ETA receptors. Capillary, but not arteriole, constriction also occurred in vivo in a mouse model of AD. Thus, inhibiting the capillary constriction caused by Aβ could potentially reduce energy lack and neurodegeneration in AD.
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