Department of Hepatobiliary Surgery, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
Key Laboratory of Immune Response and Immunotherapy, University of Science and Technology of China, Hefei, Anhui, China.
Front Immunol. 2024 Sep 20;15:1448535. doi: 10.3389/fimmu.2024.1448535. eCollection 2024.
Maintaining metabolic homeostasis is crucial for cellular and organismal health throughout their lifespans. The intricate link between metabolism and inflammation through immunometabolism is pivotal in maintaining overall health and disease progression. The multifactorial nature of metabolic and inflammatory processes makes study of the relationship between them challenging. Homologs of silent information regulator 2 protein, known as Sirtuins (SIRTs), have been demonstrated to promote longevity in various organisms. As nicotinamide adenine dinucleotide-dependent deacetylases, members of the Sirtuin family (SIRT1-7) regulate energy metabolism and inflammation. In this review, we provide an extensive analysis of SIRTs involved in regulating key metabolic pathways, including glucose, lipid, and amino acid metabolism. Furthermore, we systematically describe how the SIRTs influence inflammatory responses by modulating metabolic pathways, as well as inflammatory cells, mediators, and pathways. Current research findings on the preferential roles of different SIRTs in metabolic disorders and inflammation underscore the potential of SIRTs as viable pharmacological and therapeutic targets. Future research should focus on the development of promising compounds that target SIRTs, with the aim of enhancing their anti-inflammatory activity by influencing metabolic pathways within inflammatory cells.
维持代谢稳态对于细胞和生物体在整个生命周期中的健康至关重要。通过免疫代谢,代谢和炎症之间的复杂联系对于维持整体健康和疾病进展至关重要。代谢和炎症过程的多因素性质使得研究它们之间的关系具有挑战性。沉默信息调节因子 2 蛋白的同源物,称为沉默调节蛋白(Sirtuins,SIRTs),已被证明可在各种生物体中促进长寿。作为烟酰胺腺嘌呤二核苷酸依赖性去乙酰化酶,Sirtuin 家族(SIRT1-7)成员调节能量代谢和炎症。在这篇综述中,我们广泛分析了参与调节关键代谢途径的 SIRTs,包括葡萄糖、脂质和氨基酸代谢。此外,我们系统地描述了 SIRTs 如何通过调节代谢途径以及炎症细胞、介质和途径来影响炎症反应。目前关于不同 SIRTs 在代谢紊乱和炎症中优先作用的研究结果强调了 SIRTs 作为可行的药理学和治疗学靶点的潜力。未来的研究应侧重于开发针对 SIRTs 的有前途的化合物,旨在通过影响炎症细胞内的代谢途径来增强其抗炎活性。