Laboratory of Cellular Neurobiology, Department of Physiology, School of Medicine, La Laguna University Tenerife, Spain.
Front Physiol. 2011 Jun 3;2:23. doi: 10.3389/fphys.2011.00023. eCollection 2011.
Emerging data suggest that compartmentalization of signaling molecules into particular membrane compartments, or lipid rafts, may be at the basis of numerous activities related to neuronal preservation against different pathologies. These signaling platforms (signalosomes) are formed by complex lipid and protein that may interact to develop a plethora of different physiological responses upon activation by different extracellular stimuli, thereby contributing to neuroprotection. One of the first studied signalosomes involved in neuroprotection against Alzheimer's disease (AD) is constituted by estrogen receptor (ER), in association with scaffolding caveolin-1 and a voltage-dependent anion channel (VDAC). In this complex, ER plays a neuroprotective role partially through the modulation of VDAC activation, a porin involved in amyloid-beta-induced toxicity. Interestingly, ER and VDAC interactions appear to be altered in lipid rafts of AD brains, a phenomenon that may contribute to neuronal impairment. Alterations in lipid components of these subdomains may contribute to destabilization of this macrocomplex. These recent advances in the relevance of signaling platforms related to brain preservation, in particular against AD, are discussed in this work.
新出现的数据表明,信号分子在特定膜隔室(或脂质筏)中的分隔可能是许多与神经元保护免受不同病理相关的活动的基础。这些信号平台(信号体)由复杂的脂质和蛋白质组成,它们可能相互作用,在受到不同细胞外刺激激活后,产生大量不同的生理反应,从而有助于神经保护。最早研究的与阿尔茨海默病(AD)神经保护相关的信号体之一是由雌激素受体(ER)组成,与支架蛋白 caveolin-1 和电压依赖性阴离子通道(VDAC)相关联。在这个复合物中,ER 通过调节 VDAC 的激活发挥神经保护作用,VDAC 是一种参与淀粉样β诱导毒性的孔蛋白。有趣的是,ER 和 VDAC 的相互作用似乎在 AD 大脑的脂质筏中发生了改变,这种现象可能导致神经元损伤。这些亚域的脂质成分的改变可能导致这个大分子复合物的不稳定。本文讨论了与大脑保护相关的信号平台(特别是针对 AD)的这些新进展的相关性。