Department of Pharmacology and Toxicology, University of Kansas, Lawrence, KS 66045, USA.
Neurobiol Aging. 2010 Dec;31(12):2146-59. doi: 10.1016/j.neurobiolaging.2008.11.005. Epub 2008 Dec 31.
Brain aging is associated with a progressive decline in cognitive function though the molecular mechanisms remain unknown. Functional changes in brain neurons could be due to age-related alterations in levels of specific proteins critical for information processing. Specialized membrane microdomains known as 'lipid rafts' contain protein complexes involved in many signal transduction processes. This study was undertaken to determine if two-dimensional fluorescence difference gel electrophoresis (2D DIGE) analysis of proteins in synaptic membrane lipid rafts revealed age-dependent alterations in levels of raft proteins. Five pairs of young and aged rat synaptic membrane rafts were subjected to DIGE separation, followed by image analysis and identification of significantly altered proteins. Of 1046 matched spots on DIGE gels, 94 showed statistically significant differences in levels between old and young rafts, and 87 of these were decreased in aged rafts. The 41 most significantly altered (p<0.03) proteins included several synaptic proteins involved in energy metabolism, redox homeostasis, and cytoskeletal structure. This may indicate a disruption in bioenergetic balance and redox homeostasis in synaptic rafts with brain aging. Differential levels of representative identified proteins were confirmed by immunoblot analysis. Our findings provide novel pathways in investigations of mechanisms that may contribute to altered neuronal function in aging brain.
脑老化与认知功能的逐渐下降有关,但分子机制尚不清楚。脑神经元的功能变化可能是由于与年龄相关的特定蛋白质水平的改变,这些蛋白质对信息处理至关重要。专门的膜微区称为“脂筏”,其中包含参与许多信号转导过程的蛋白质复合物。本研究旨在确定突触膜脂筏中的蛋白质的二维荧光差异凝胶电泳(2D DIGE)分析是否揭示了与年龄相关的筏蛋白水平的改变。将五对年轻和老年大鼠突触膜筏进行 DIGE 分离,然后进行图像分析和鉴定明显改变的蛋白质。在 DIGE 凝胶上的 1046 个匹配斑点中,有 94 个显示在老年和年轻筏之间的水平存在统计学上的显著差异,其中 87 个在老年筏中减少。最显著改变的 41 种蛋白质(p<0.03)包括几种参与能量代谢、氧化还原平衡和细胞骨架结构的突触蛋白。这可能表明在突触筏中生物能量平衡和氧化还原平衡的破坏与大脑老化有关。通过免疫印迹分析证实了代表性鉴定蛋白质的差异水平。我们的发现为研究可能导致衰老大脑中神经元功能改变的机制提供了新的途径。