Connecting aging biology and inflammation in the omics era

被引:104
作者
Walker, Keenan A. [1 ]
Basisty, Nathan [1 ]
Wilson, David M., III [2 ]
Ferrucci, Luigi [1 ]
机构
[1] NIA, Intramural Res Program, NIH, Baltimore, MD 21224 USA
[2] Hasselt Univ, Biomed Res Inst, Fac Med & Life Sci, Diepenbeek, Belgium
基金
美国国家卫生研究院;
关键词
NF-KAPPA-B; BLOOD-BRAIN-BARRIER; HUMAN IMMUNE-SYSTEM; CELLULAR SENESCENCE; RISK-FACTORS; DNA-DAMAGE; ACTIVATION; CELLS; DISEASE; MICROGLIA;
D O I
10.1172/JCI158448
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Aging is characterized by the accumulation of damage to macromolecules and cell architecture that triggers a proinflammatory state in blood and solid tissues, termed inflammaging. Inflammaging has been implicated in the pathogenesis of many age-associated chronic diseases as well as loss of physical and cognitive function. The search for mechanisms that underlie inflammaging focused initially on the hallmarks of aging, but it is rapidly expanding in multiple directions. Here, we discuss the threads connecting cellular senescence and mitochondrial dysfunction to impaired mitophagy and DNA damage, which may act as a hub for inflammaging. We explore the emerging multi-omics efforts that aspire to define the complexity of inflammaging ??? and identify molecular signatures and novel targets for interventions aimed at counteracting excessive inflammation and its deleterious consequences while preserving the physiological immune response. Finally, we review the emerging evidence that inflammation is involved in brain aging and neurodegenerative diseases. Our goal is to broaden the research agenda for inflammaging with an eye on new therapeutic opportunities.
引用
收藏
页数:13
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