Biochemical Proteomics Group, Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany.
Department of Biochemistry and Immunochemistry, Wroclaw Medical University, 50-368 Wrocław, Poland.
Int J Mol Sci. 2021 Jun 8;22(12):6188. doi: 10.3390/ijms22126188.
Aging is associated with a general decline of cognitive functions, and it is widely accepted that this decline results from changes in the expression of proteins involved in regulation of synaptic plasticity. However, several lines of evidence have accumulated that suggest that the impaired function of the aged brain may be related to significant alterations in the energy metabolism. In the current study, we employed the label-free "Total protein approach" (TPA) method to focus on the similarities and differences in energy metabolism proteomes of young (1-month-old) and aged (22-month-old) murine brains. We quantified over 7000 proteins in each of the following three analyzed brain structures: the hippocampus, the cerebral cortex and the cerebellum. To the best of our knowledge, this is the most extensive quantitative proteomic description of energy metabolism pathways during the physiological aging of mice. The analysis demonstrates that aging does not significantly affect the abundance of total proteins in the studied brain structures, however, the levels of proteins constituting energy metabolism pathways differ significantly between young and aged mice.
衰老是认知功能普遍下降的一个标志,人们普遍认为这种下降是由于参与调节突触可塑性的蛋白质表达发生变化所致。然而,有几条证据线表明,衰老大脑的功能受损可能与能量代谢的显著改变有关。在目前的研究中,我们采用了无标记的“全蛋白质方法”(TPA),重点研究了年轻(1 个月大)和年老(22 个月大)鼠脑的能量代谢蛋白质组之间的相似性和差异。我们对以下三个分析的脑结构中的每个结构进行了超过 7000 种蛋白质的定量:海马体、大脑皮层和小脑。据我们所知,这是对小鼠生理衰老过程中能量代谢途径进行的最广泛的定量蛋白质组描述。分析表明,衰老不会显著影响研究中脑结构内总蛋白质的丰度,然而,构成能量代谢途径的蛋白质水平在年轻和年老的小鼠之间存在显著差异。