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微小 RNA-570 是细胞衰老和炎症老化的新型调节因子。

MicroRNA-570 is a novel regulator of cellular senescence and inflammaging.

机构信息

Airway Disease Section, National Heart and Lung Institute, Imperial College London, London, United Kingdom.

出版信息

FASEB J. 2019 Feb;33(2):1605-1616. doi: 10.1096/fj.201800965R. Epub 2018 Aug 29.

DOI:10.1096/fj.201800965R
PMID:30156909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6338629/
Abstract

Diseases of accelerated aging often occur together (multimorbidity), and their prevalence is increasing, with high societal and health care costs. Chronic obstructive pulmonary disease (COPD) is one such condition, in which one half of patients exhibit ≥4 age-related diseases. Diseases of accelerated aging share common molecular pathways, which lead to the detrimental accumulation of senescent cells. These senescent cells no longer divide but release multiple inflammatory proteins, known as the senescence-associated secretory phenotype, which may perpetuate and speed disease. Here, we show that inhibiting miR-570-3p, which is increased in COPD cells, reverses cellular senescence by restoring the antiaging molecule sirtuin-1. MiR-570-3p is induced by oxidative stress in airway epithelial cells through p38 MAP kinase-c-Jun signaling and drives senescence by inhibiting sirtuin-1. Inhibition of elevated miR-570-3p in COPD small airway epithelial cells, using an antagomir, restores sirtuin-1 and suppresses markers of cellular senescence (p16, p21, and p27), thereby restoring cellular growth by allowing progression through the cell cycle. MiR-570-3p inhibition also suppresses the senescence-associated secretory phenotype (matrix metalloproteinases-2/9, C-X-C motif chemokine ligand 8, IL-1β, and IL-6). Collectively, these data suggest that inhibiting miR-570-3p rejuvenates cells via restoration of sirtuin-1, reducing many of the abnormalities associated with cellular senescence.-Baker, J. R., Vuppusetty, C., Colley, T., Hassibi, S., Fenwick, P. S., Donnelly, L. E., Ito, K., Barnes, P. J. MicroRNA-570 is a novel regulator of cellular senescence and inflammaging.

摘要

加速衰老相关疾病常同时发生(共病),其患病率在增加,给社会和医疗保健带来了沉重负担。慢性阻塞性肺疾病(COPD)就是这样一种疾病,其中一半患者表现出≥4 种与年龄相关的疾病。加速衰老相关疾病具有共同的分子途径,导致衰老细胞的有害积累。这些衰老细胞不再分裂,但会释放多种炎症蛋白,称为衰老相关分泌表型,这可能会促使和加速疾病的发生。在这里,我们表明,抑制 COPD 细胞中上调的 miR-570-3p 可以通过恢复抗衰老分子 Sirtuin-1 来逆转细胞衰老。miR-570-3p 是由气道上皮细胞中的氧化应激通过 p38 MAP 激酶-c-Jun 信号通路诱导的,通过抑制 Sirtuin-1 来驱动衰老。用反义核苷酸抑制 COPD 小气道上皮细胞中升高的 miR-570-3p,可恢复 Sirtuin-1 并抑制细胞衰老的标志物(p16、p21 和 p27),从而通过允许细胞周期进展来恢复细胞生长。miR-570-3p 抑制还抑制了衰老相关分泌表型(基质金属蛋白酶-2/9、C-X-C 基序趋化因子配体 8、IL-1β 和 IL-6)。总的来说,这些数据表明,抑制 miR-570-3p 通过恢复 Sirtuin-1 使细胞恢复活力,减少了许多与细胞衰老相关的异常。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25b/6338629/16c8dd0d08d4/fj.201800965Rf7.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25b/6338629/16c8dd0d08d4/fj.201800965Rf7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25b/6338629/6868ae1944b5/fj.201800965Rf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25b/6338629/0a57ff90b2c2/fj.201800965Rf2.jpg
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