Amadoruge Pavithra C, Barnham Kevin J
Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, 30 Flemington Road, Parkville, VIC 3010, Australia.
Int J Alzheimers Dis. 2011 Mar 2;2011:542043. doi: 10.4061/2011/542043.
Alzheimer's disease (AD) is a debilitating form of dementia. The hallmark protein associated with the disease is the amyloid beta (Aβ) peptide. Aggregation of Aβ has been shown to depend on interactions with metals. The recent studies now demonstrate that metals also play additional important roles in the disease process. Consequently, there may be benefit from modulating metal homeostasis. However, the role and subcellular location of metals within neurons is not well understood. There is growing evidence to suggest that metals can act at the site of cellular membrane receptors and affect cellular signaling by modulating the signal transduction of those receptors. The glutamatergic and cholinergic receptor systems, both well-known neurotransmitter systems affected in AD, have well-documented metal interactions, as do the tropomyosin-receptor kinase (Trk) family of receptors and the epidermal growth factor (EGF) receptor. In this paper, the metal interactions with these membrane receptor systems will be explored and thus the potential for membrane receptors as an intervention point in AD will be assessed.
阿尔茨海默病(AD)是一种使人衰弱的痴呆症形式。与该疾病相关的标志性蛋白是β-淀粉样蛋白(Aβ)肽。已表明Aβ的聚集依赖于与金属的相互作用。最近的研究现在证明,金属在疾病过程中还发挥着其他重要作用。因此,调节金属稳态可能有益。然而,金属在神经元内的作用和亚细胞定位尚不清楚。越来越多的证据表明,金属可作用于细胞膜受体部位,并通过调节这些受体的信号转导来影响细胞信号传导。谷氨酸能和胆碱能受体系统是AD中受影响的两个著名神经递质系统,它们与金属的相互作用已得到充分记录,原肌球蛋白受体激酶(Trk)家族受体和表皮生长因子(EGF)受体也是如此。在本文中,将探讨金属与这些膜受体系统的相互作用,从而评估膜受体作为AD干预靶点的潜力。