小RNA
背景(考古学)
表观遗传学
全身炎症
多样性(控制论)
生物
炎症
免疫学
基因
遗传学
计算机科学
古生物学
人工智能
作者
Olivieri Fabiola,Francesco Prattichizzo,Angelica Giuliani,Giulia Matacchione,Maria Rita Rippo,Jacopo Sabbatinelli,Massimiliano Bonafè
标识
DOI:10.1016/j.arr.2021.101374
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI