Department of Clinical and Molecular Sciences, DISCLIMO, Università Politecnica delle Marche, Ancona, Italy; Center of Clinical Pathology and Innovative Therapy, IRCCS INRCA, Ancona, Italy.
IRCCS MultiMedica, Milano, Italy.
Ageing Res Rev. 2021 Sep;70:101374. doi: 10.1016/j.arr.2021.101374. Epub 2021 May 31.
The first paper on "inflammaging" published in 2001 paved the way for a unifying theory on how and why aging turns out to be the main risk factor for the development of the most common age-related diseases (ARDs). The most exciting challenge on this topic was explaining how systemic inflammation steeps up with age and why it shows different rates among individuals of the same chronological age. The "epigenetic revolution" in the past twenty years conveyed that the assessment of the individual genetic make-up is not enough to depict the trajectories of age-related inflammation. Accordingly, others and we have been focusing on the role of non-coding RNA, i.e. microRNAs (miRNAs), in inflammaging. The results obtained in the latest 10 years underpinned the key role of a miRNA subset that we have called inflammamiRs, owing to their ability to master (NF-κB)-driven inflammatory pathways. In this review, we will focus on two inflammamiRs, i.e. miR-21-5p and miR-146a-5p, which target a variety of molecules belonging to the NF-κB/NLRP3 pathways. The interplay between miR-146a-5p and IL-6 in the context of aging and ARDs will also be highlighted. We will also provide the most relevant evidence suggesting that circulating inflammamiRs, along with IL-6, can measure the degree of inflammaging.
2001 年发表的第一篇关于“炎症衰老”的论文为如何以及为何衰老成为大多数与年龄相关的疾病 (ARDs) 发展的主要风险因素提供了一个统一的理论。在这个主题上最令人兴奋的挑战是解释全身炎症如何随着年龄的增长而加剧,以及为什么它在相同年龄的个体中有不同的速度。在过去的二十年里,“表观遗传学革命”表明,评估个体的遗传构成不足以描述与年龄相关的炎症的轨迹。因此,其他人,包括我们,一直专注于非编码 RNA(即 microRNAs (miRNAs))在炎症衰老中的作用。在过去 10 年中获得的结果支持了我们称之为“炎症 miRNA”的 miRNA 子集的关键作用,因为它们能够控制(NF-κB)驱动的炎症途径。在这篇综述中,我们将重点介绍两种炎症 miRNA,即 miR-21-5p 和 miR-146a-5p,它们靶向属于 NF-κB/NLRP3 途径的多种分子。我们还将强调 miR-146a-5p 和 IL-6 之间在衰老和 ARD 背景下的相互作用。我们还将提供最相关的证据表明,循环炎症 miRNA 与 IL-6 一起可以衡量炎症衰老的程度。