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定量蛋白质组学分析与大鼠肝组织衰老和热量限制相关的变化。

Quantitative Proteomic Analysis of Changes Related to Age and Calorie Restriction in Rat Liver Tissue.

机构信息

BK21 Plus KNU Multi-Omics Based Creative Drug Research Team, College of Pharmacy, Research Institute of Pharmaceutical Sciences, Kyungpook National University, Daegu, Republic of Korea.

Center for Plant Aging Research, Institute for Basic Science, Daegu, Republic of Korea.

出版信息

Proteomics. 2018 Mar;18(5-6):e1700240. doi: 10.1002/pmic.201700240.

DOI:10.1002/pmic.201700240
PMID:29280565
Abstract

Calorie restriction (CR) is the most frequently studied mechanism for increasing longevity, protecting against stress, and delaying age-associated diseases. Most studies have initiated CR in young animals to determine the protective effects against aging. Although aging phenomena are well-documented, the molecular mechanisms of aging and CR remain unclear. In this study, we observe changes in hepatic proteins upon age-related and diet-restricted changes in the rat liver using quantitative proteomics. Quantitative proteomes are measured using tandem mass tag labeling followed by LC-MS/MS. We compare protein levels in livers from young (6 months old) and old (25 months old) rats with 40% calorie-restricted (YCR and OCR, respectively) or ad libitum diets. In total, 44 279 peptides and 3134 proteins are identified and 260 differentially expressed proteins are found. Functional enrichment analysis show that these proteins are mainly involved in glucose and fatty acid metabolism-related processes, consistent with the theory that energy metabolism regulation is dependent on age-related and calorie-restricted changes in liver tissue. In addition, proteins mediating inflammation and gluconeogenesis are increased in OCR livers, but not YCR livers. These results show that CR in old rats might not have antiaging benefits because liver inflammation is increased.

摘要

热量限制(CR)是研究最多的延长寿命、抵抗压力和延缓与年龄相关疾病的机制。大多数研究都是在年轻动物中启动 CR,以确定对衰老的保护作用。尽管衰老现象已有充分的记录,但衰老和 CR 的分子机制仍不清楚。在这项研究中,我们使用定量蛋白质组学观察到与年龄相关和饮食限制的大鼠肝脏中肝蛋白的变化。使用串联质量标签标记和 LC-MS/MS 测量定量蛋白质组。我们比较了年轻(6 个月大)和年老(25 个月大)大鼠肝脏中 40%热量限制(YCR 和 OCR)或自由饮食的蛋白质水平。总共鉴定出 44279 个肽和 3134 个蛋白质,发现 260 个差异表达的蛋白质。功能富集分析表明,这些蛋白质主要参与葡萄糖和脂肪酸代谢相关过程,这与能量代谢调节依赖于肝组织与年龄相关和热量限制的变化的理论一致。此外,在 OCR 肝脏中,介导炎症和糖异生的蛋白质增加,但在 YCR 肝脏中没有增加。这些结果表明,老年大鼠的 CR 可能没有抗衰老益处,因为肝脏炎症增加。

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