课题基金 / 基金详情

Brain pericyte contractility, cerebral blood flow and blood-brain barrier integrity are impaired by normal aging and Alzheimer's disease amyloid-beta and are dependent on p75NTR

Brain pericyte contractility, cerebral blood flow and blood-brain barrier integrity are impaired by normal aging and Alzheimer's disease amyloid-beta and are dependent on p75NTR
大脑周细胞收缩力、脑血流量和血脑屏障完整性受到正常衰老和阿尔茨海默病β淀粉样蛋白的损害,并且依赖于 p75NTR
批准号:
10459419
负责人:
Amy R Nelson
金额:
$21.82万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-07-15 至 2023-12-31

项目摘要

项目成果

Amy R Nelson的其他基金

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中文摘要
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英文摘要
PROJECT SUMMARY/ ABSTRACT Neurovascular dysfunction has been linked to Alzheimer’s disease (AD) evolution in experimental, imaging, pathological, and epidemiological studies. These key findings have led to an emerging ‘neurovascular hypothesis’ of AD, which holds that cerebrovascular dysfunction contributes to the onset and progression of cognitive decline. There is growing appreciation and strong evidence that neurovascular uncoupling, cerebral blood flow (CBF) reductions and dysregulation, and breakdown of the blood-brain barrier (BBB), including the loss of pericytes, are early events in the AD pathophysiological cascade. Pericytes are mural cells on capillaries that are critical for the maintenance of the BBB, and have recently been implicated in the regulation of CBF. Importantly, pericytes deteriorate and the BBB degrades in AD. Based on our preliminary findings we hypothesize that pericytes are contractile cells that regulate capillary diameter and thereby CBF, and BBB integrity, and that this pericyte regulation is impaired in normal aging and in the presence of Aβ40 and Aβ42 via p75NTR pathway. To test this hypothesis, I will use cutting-edge approaches including in vivo two- photon/confocal brain vascular imaging to assess pericyte contractility, capillary diameter, CBF changes and BBB integrity. Brain tissue analysis will also be performed. I will determine if brain pericytes retain contractility, properly regulate CBF, and maintain BBB integrity in normal aging and in the presence of Aβ40 and Aβ42 (AIM 1/ K99). Also, I will determine if normal aging and Aβ40 and Aβ42 impair brain BBB integrity via p75NTR (AIM 2/ R00). Understanding how pericytes regulate CBF and BBB integrity in normal aging and AD and the involvement and potential of p75NTR as a therapeutic target for AD is timely and important. This K99/R00 grant is essential for my success in becoming an impactful tenure-track assistant professor because it provides me training in an essential technique to investigate neurovascular dynamics for future studies, and also will provide professional training in improving oral presentation and grant writing skills.
期刊论文(3)
专著(0)
科研奖励(0)
会议论文
DOI: 10.3389/fnagi.2022.980561
发表时间: 2022
期刊: Frontiers in aging neuroscience
影响因子: 4.8
作者: []
通讯作者:
DOI: 10.3389/fnagi.2022.858429
发表时间: 2022
期刊: Frontiers in aging neuroscience
影响因子: 4.8
作者: []
通讯作者:
Vascular cognitive impairment and dementia: An early career researcher perspective.
血管认知障碍和痴呆:早期职业研究员的观点。
DOI: 10.1002/dad2.12310
发表时间: 2022
期刊: ALZHEIMER'S & DEMENTIA: DIAGNOSIS, ASSESSMENT & DISEASE MONITORING
影响因子: 5.3
作者: [Silva, Narlon C Boa Sorte, Bracko, Oliver, Nelson, Amy R, de Oliveira, Fabricio Ferreira, Robison, Lisa S, Shaaban, C Elizabeth, Hainsworth, Atticus H, Price, Brittani R]
通讯作者: Price, Brittani R