Czeczor J K, McGee S L
Metabolic Research Unit, Metabolic Reprogramming Laboratory, School of Medicine and Centre for Molecular and Medical Research, Deakin University, Geelong, VIC, Australia.
Institute for Clinical Diabetology, German Diabetes Center, Leibniz Center for Diabetes Research, Heinrich-Heine University, Düsseldorf, Germany.
J Neuroendocrinol. 2017 May;29(5). doi: 10.1111/jne.12470.
The amyloid precursor protein (APP) is a transmembrane protein that can be cleaved by proteases through two different pathways to yield a number of small peptides, each with distinct physiological properties and functions. It has been extensively studied in the context of Alzheimer's disease, with the APP-derived amyloid β (Aβ) peptide being a major constituent of the amyloid plaques observed in this disease. It has been known for some time that APP can regulate neuronal metabolism; however, the present review examines the evidence indicating that APP and its peptides can also regulate key metabolic processes such as insulin action, lipid synthesis and storage and mitochondrial function in peripheral tissues. This review presents the hypothesis that amyloidogenic processing of APP in peripheral tissues plays a key role in the response to nutrient excess and that this could contribute to the pathogenesis of metabolic diseases such as obesity and type 2 diabetes (T2D).
淀粉样前体蛋白(APP)是一种跨膜蛋白,可被蛋白酶通过两种不同途径切割,产生多种小肽,每种小肽都具有独特的生理特性和功能。在阿尔茨海默病的背景下,它已得到广泛研究,APP衍生的淀粉样β(Aβ)肽是该疾病中观察到的淀粉样斑块的主要成分。人们早就知道APP可以调节神经元代谢;然而,本综述探讨了相关证据,这些证据表明APP及其肽还可以调节外周组织中的关键代谢过程,如胰岛素作用、脂质合成与储存以及线粒体功能。本综述提出了一个假说,即外周组织中APP的淀粉样生成过程在对营养过剩的反应中起关键作用,这可能有助于肥胖和2型糖尿病(T2D)等代谢性疾病的发病机制。