Center of Excellence for Aging and Brain Repair, Departments of Neurosurgery and Brain Repair, and Molecular Pharmacology and Physiology, USF Morsani College of Medicine, 12901 Bruce B. Downs Blvd, MDC 78, Tampa, FL 33612, USA.
Research Service, James A Haley VA Hospital, Tampa, FL 33620, USA.
Int J Mol Sci. 2021 Jun 14;22(12):6373. doi: 10.3390/ijms22126373.
Microglial activity in the aging neuroimmune system is a central player in aging-related dysfunction. Aging alters microglial function via shifts in protein signaling cascades. These shifts can propagate neurodegenerative pathology. Therapeutics require a multifaceted approach to understand and address the stochastic nature of this process. Polyphenols offer one such means of rectifying age-related decline. Our group used mass spectrometry (MS) analysis to explicate the complex nature of these aging microglial pathways. In our first experiment, we compared primary microglia isolated from young and aged rats and identified 197 significantly differentially expressed proteins between these groups. Then, we performed bioinformatic analysis to explore differences in canonical signaling cascades related to microglial homeostasis and function with age. In a second experiment, we investigated changes to these pathways in aged animals after 30-day dietary supplementation with NT-020, which is a blend of polyphenols. We identified 144 differentially expressed proteins between the NT-020 group and the control diet group via MS analysis. Bioinformatic analysis predicted an NT-020 driven reversal in the upregulation of age-related canonical pathways that control inflammation, cellular metabolism, and proteostasis. Our results highlight salient aspects of microglial aging at the level of protein interactions and demonstrate a potential role of polyphenols as therapeutics for age-associated dysfunction.
衰老神经免疫系统中的小胶质细胞活性是与衰老相关功能障碍的核心因素。衰老通过蛋白质信号级联的转变改变小胶质细胞功能。这些转变会导致神经退行性病理。治疗需要采用多方面的方法来理解和解决这个过程的随机性。多酚提供了一种纠正与年龄相关下降的方法。我们的小组使用质谱 (MS) 分析来阐明这些衰老小胶质细胞途径的复杂性质。在我们的第一个实验中,我们比较了从小鼠和老年大鼠中分离出的原代小胶质细胞,并在这些组之间鉴定了 197 种明显差异表达的蛋白质。然后,我们进行了生物信息学分析,以探索与小胶质细胞动态平衡和功能相关的经典信号通路随年龄的变化。在第二个实验中,我们研究了在 NT-020 饮食补充 30 天后,这些通路在老年动物中的变化,NT-020 是一种多酚混合物。我们通过 MS 分析在 NT-020 组和对照饮食组之间鉴定了 144 种差异表达的蛋白质。生物信息学分析预测,NT-020 驱动与炎症、细胞代谢和蛋白质稳态相关的与年龄相关的经典途径的上调逆转。我们的结果突出了小胶质细胞衰老在蛋白质相互作用水平上的显著方面,并表明多酚作为治疗与年龄相关的功能障碍的潜在作用。