Vascular mTOR-dependent mechanisms linking the control of aging to Alzheimer's disease

被引:28
|
作者
Galvan, Veronica [1 ,2 ]
Hart, Matthew J. [3 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Dept Physiol, 15355 Lambda Dr, San Antonio, TX 78245 USA
[2] Univ Texas Hlth Sci Ctr San Antonio, Barshop Inst Longev & Aging Studies, 15355 Lambda Dr, San Antonio, TX 78245 USA
[3] Univ Texas Hlth Sci Ctr San Antonio, Dept Biochem, 15355 Lambda Dr, San Antonio, TX 78245 USA
关键词
Alzheimer's; Neurovascular aging; Target of rapamycin; MTOR; Aging; Geroscience; BLOOD-BRAIN-BARRIER; AMYLOID-BETA-PEPTIDE; SMOOTH-MUSCLE-CELLS; NITRIC-OXIDE SYNTHASE; RECEPTOR-RELATED PROTEIN; NICOTINIC ACETYLCHOLINE-RECEPTORS; CEREBRAL-ISCHEMIA-REPERFUSION; SIROLIMUS-ELUTING STENTS; AGE-RELATED-CHANGES; EXTENDS LIFE-SPAN;
D O I
10.1016/j.bbadis.2015.11.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aging is the strongest known risk factor for Alzheimer's disease (AD). With the discovery of the mechanistic target of rapamycin (mTOR) as a critical pathway controlling the rate of aging in mice, molecules at the interface between the regulation of aging and the mechanisms of specific age-associated diseases can be identified. We will review emerging evidence that mTOR-dependent brain vascular dysfunction, a universal feature of aging, may be one of the mechanisms linking the regulation of the rate of aging to the pathogenesis of Alzheimer's disease. This article is part of a Special Issue entitled: Vascular Contributions to Cognitive Impairment and Dementia edited by M. Paul Murphy, Roderick A. Corriveau and Donna M. Wilcock. Published by Elsevier B.V.
引用
收藏
页码:992 / 1007
页数:16
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