The Emergence of Model Systems to Investigate the Link Between Traumatic Brain Injury and Alzheimer's Disease

被引:6
作者
Srinivasan, Gayathri [1 ]
Brafman, David A. [1 ]
机构
[1] Arizona State Univ, Sch Biol & Hlth Syst Engn, Tempe, AZ 85281 USA
基金
美国国家卫生研究院;
关键词
traumatic brain injury; Alzheimer's disease; in vivo models; in vitro models; pluripotent stem cells; genome engineering; AMYLOID PRECURSOR PROTEIN; IN-VITRO MODEL; IMPROVES FUNCTIONAL RECOVERY; GLYCOGEN-SYNTHASE KINASE-3; APP/PS1 MOUSE MODEL; CLOSED-HEAD INJURY; APOLIPOPROTEIN-E; TAU-PROTEIN; TRANSGENIC MICE; AXONAL INJURY;
D O I
10.3389/fnagi.2021.813544
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Numerous epidemiological studies have demonstrated that individuals who have sustained a traumatic brain injury (TBI) have an elevated risk for developing Alzheimer's disease and Alzheimer's-related dementias (AD/ADRD). Despite these connections, the underlying mechanisms by which TBI induces AD-related pathology, neuronal dysfunction, and cognitive decline have yet to be elucidated. In this review, we will discuss the various in vivo and in vitro models that are being employed to provide more definite mechanistic relationships between TBI-induced mechanical injury and AD-related phenotypes. In particular, we will highlight the strengths and weaknesses of each of these model systems as it relates to advancing the understanding of the mechanisms that lead to TBI-induced AD onset and progression as well as providing platforms to evaluate potential therapies. Finally, we will discuss how emerging methods including the use of human induced pluripotent stem cell (hiPSC)-derived cultures and genome engineering technologies can be employed to generate better models of TBI-induced AD.
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页数:16
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