The interaction between dysfunction of vasculature and tauopathy in Alzheimer's disease and related dementias

被引:1
作者
Huang, Chuyao [1 ]
Wei, Zhenwen [1 ]
Zheng, Ningxiang [1 ]
Yan, Jingsi [1 ]
Zhang, Jiayu [1 ]
Ye, Xinyi [1 ]
Zhao, Wei [1 ]
机构
[1] Guangzhou Univ Chinese Med, Sci & Technol Innovat Ctr, 12 Airport Rd, Guangzhou 510405, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease and related dementias; tauopathy; vasculature; BLOOD-BRAIN-BARRIER; AMYLOID-BETA-PEPTIDE; TAU PHOSPHORYLATION; COGNITIVE IMPAIRMENT; APOLIPOPROTEIN-E; HUMAN PLATELETS; RHO-KINASE; INTERSTITIAL FLUID; PERIPHERAL MARKER; TRANSGENIC MICE;
D O I
10.1002/alz.14618
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Tauopathy is one of the pathological features of Alzheimer's disease and related dementias (ADRD). At present, there have been many studies on the formation, deposition, and intercellular transmission of tau in neurons and immune cells. The vasculature is an important component of the central nervous system. This review discusses the interaction between vasculature and tau in detail from three aspects. (1) The vascular risk factors (VRFs) discussed in this review include diabetes mellitus (DM), abnormal blood pressure (BP), and hypercholesterolemia. (2) In ADRD pathology, the hyperphosphorylation and deposition of tau interact with disrupted vasculature, such as different cells (endothelial cells, smooth muscular cells, and pericytes), the blood-brain barrier (BBB), and the cerebral lymphatic system. (3) The functions of vasculature are regulated by various signaling transductions. Endothelial nitric oxide synthase/nitric oxide, calcium signaling, Rho/Rho-associated coiled-coil containing Kinase, and receptors for advanced glycation end products are discussed in this review. Our findings indicate that the prevention and treatment of vascular health may be a potential target for ADRD combination therapy.
引用
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页数:21
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