神经病理学
缺氧(环境)
PI3K/AKT/mTOR通路
神经科学
新皮层
痴呆
蛋白激酶B
转录组
衰老
生物
心理学
内科学
医学
疾病
信号转导
基因
细胞生物学
基因表达
化学
遗传学
有机化学
氧气
作者
Pavel Katsel,Peter Fam,Weilun Tan,Sonia Khan,Miguel A. Gama-Sosa,Rita De Gasperi,Panos Roussos,Ari Robinson,Itzik Cooper,Michal Schnaider‐Beeri,Vahram Haroutunian
摘要
Abstract Introduction Molecular responses in the brains of persons with mild cognitive impairment (MCI), the earliest transitional state between normal aging and early Alzheimer's disease (AD), are poorly understood. Methods We examined AD‐related neuropathology and transcriptome changes in the neocortex of individuals with MCI relative to controls and temporal responses to the mild hypoxia in mouse brains. Results Subsets of vascular early response to hypoxia genes were upregulated in MCI prior to the buildup of AD neuropathology. Early activation of pro‐angiogenic hypoxia‐inducible factor signaling in response to mild hypoxia was detected in mouse brains similar to those that were altered in MCI. Protracted responses to hypoxia were characterized by activation of phosphoinositide 3‐kinase (PI3K)‐protein kinase B (Akt)‐the mammalian target of rapamycin (mTOR) pathways in brain microvessel isolates. Discussion These findings suggest that cerebrovascular remodeling is an important antecedent to the development of dementia and a component of the homeostatic response to reduced oxygen tension in aging prior to the onset of AD.
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