Habib Ahsan, Sawmiller Darrell, Tan Jun
Rashid Laboratory for Developmental Neurobiology, Silver Child Development Center, Department of Psychiatry and Behavioral Neurosciences, Morsani College of Medicine, University of South Florida, Tampa, Florida, USA.
J Neurosci Res. 2017 Apr;95(4):973-991. doi: 10.1002/jnr.23823. Epub 2016 Aug 17.
Soluble amyloid precursor protein α (sAPPα), a secreted proteolytic fragment of nonamyloidogenic amyloid precursor protein (APP) processing, is known for numerous neuroprotective functions. These functions include but are not limited to proliferation, neuroprotection, synaptic plasticity, memory formation, neurogenesis, and neuritogenesis in cell culture and animal models. In addition, sAPPα influences amyloid-β (Aβ) production by direct modulation of APP β-secretase proteolysis as well as Aβ-related or unrelated tau pathology, hallmark pathologies of Alzheimer's disease (AD). Thus, the restoration of sAPPα levels and functions in the brain by increasing nonamyloidogenic APP processing and/or manipulation of its signaling could reduce AD pathology and cognitive impairment. It is likely that identification and characterization of sAPPα receptors in the brain, downstream effectors, and signaling pathways will pave the way for an attractive therapeutic target for AD prevention or intervention. © 2016 Wiley Periodicals, Inc.
可溶性淀粉样前体蛋白α(sAPPα)是淀粉样前体蛋白(APP)非淀粉样生成性加工过程中分泌的蛋白水解片段,因其众多神经保护功能而闻名。这些功能包括但不限于细胞培养和动物模型中的增殖、神经保护、突触可塑性、记忆形成、神经发生和神经突形成。此外,sAPPα通过直接调节APPβ-分泌酶蛋白水解以及阿尔茨海默病(AD)的标志性病理——与淀粉样β(Aβ)相关或不相关的tau病理,来影响Aβ的产生。因此,通过增加非淀粉样生成性APP加工和/或操纵其信号传导来恢复大脑中sAPPα的水平和功能,可能会减少AD病理和认知障碍。大脑中sAPPα受体、下游效应器和信号通路的鉴定与表征,很可能为AD预防或干预提供一个有吸引力的治疗靶点。©2016威利期刊公司。