SIRT1在衰老和免疫衰老中的调节作用。
Regulatory Roles for SIRT1 in Aging and Immunosenescence.
作者信息
Brissett-Lasalle Devonique, Syed Zoya, Yarubandi Yashitha, Leips Jeff, Green Erin
机构信息
Department of Biological Sciences, University of Maryland Baltimore County, Baltimore, MD, USA.
Marlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland School of Medicine, Baltimore, MD, USA.
出版信息
Results Probl Cell Differ. 2025;75:291-308. doi: 10.1007/978-3-031-91459-1_10.
Silent information regulator 1 (SIRT1), a conserved lysine deacetylase, is an important contributor to the function of macrophages, which are the scavengers of the innate immune system. Macrophages are part of the first line of defense against infection and key players in immunity due to their ability to survey tissue for infections or damage, release inflammatory cytokines, and clear pathogens. Macrophage function deteriorates with age and is a common indicator of immunosenescence. SIRT1 is known to influence multiple aspects of macrophage physiology, particularly proliferation, self-renewal, migration, the regulation of macrophage polarization, and the ability of macrophages to clear pathogens via phagocytosis and inflammasome signaling. Furthermore, mammalian SIRT1 and orthologous Sir2 in other organisms have well-defined roles in aging. Therefore, in this chapter, we discuss evidence that links SIRT1 to macrophage behavior and function, explore its role in inflammatory pathways linked to aging, and highlight key research questions in immunosenescence and the implications for epigenetic and non-epigenetic roles of SIRT1.
沉默信息调节因子1(SIRT1)是一种保守的赖氨酸脱乙酰酶,是巨噬细胞功能的重要贡献者,巨噬细胞是固有免疫系统的清道夫。巨噬细胞是抵御感染的第一道防线的一部分,由于它们能够监测组织是否受到感染或损伤、释放炎性细胞因子并清除病原体,因此是免疫的关键参与者。巨噬细胞功能会随着年龄增长而衰退,是免疫衰老的常见指标。已知SIRT1会影响巨噬细胞生理学的多个方面,特别是增殖、自我更新、迁移、巨噬细胞极化的调节,以及巨噬细胞通过吞噬作用和炎性小体信号清除病原体的能力。此外,哺乳动物的SIRT1和其他生物体中的直系同源Sir2在衰老过程中具有明确的作用。因此,在本章中,我们将讨论将SIRT1与巨噬细胞行为和功能联系起来的证据,探讨其在与衰老相关的炎症途径中的作用,并突出免疫衰老中的关键研究问题以及SIRT1的表观遗传和非表观遗传作用的影响。