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微小RNA-21:浆细胞样树突状细胞产生I型和III型干扰素的最佳正调控因子

MicroRNA-21: A Positive Regulator for Optimal Production of Type I and Type III Interferon by Plasmacytoid Dendritic Cells.

作者信息

Liu Fang, Liu Chunxi, Hu Xiaoyu, Shang Yingli, Wu Li

机构信息

Institute for Immunology and School of Medicine, Tsinghua University, Beijing, China.

College of Veterinary Medicine, Shandong Agricultural University, Taian, China.

出版信息

Front Immunol. 2017 Aug 21;8:947. doi: 10.3389/fimmu.2017.00947. eCollection 2017.

DOI:10.3389/fimmu.2017.00947
PMID:28871250
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5567078/
Abstract

Plasmacytoid dendritic cells (pDCs) are the major producers of type I and type III interferons (IFNs) that play essential roles in host antiviral immunity. MicroRNAs (miRs) are small, noncoding RNAs that can modulate many immune processes. Although molecular regulation of type I IFN production by pDCs has been studied extensively, the regulation of type III IFN production has not been studied thoroughly, particularly at posttranscriptional level. We show here that miR-21 is an essential positive regulator for the production of both IFN-α and IFN-λ by pDCs and for promoting host defense against viral infection. miR-21 was markedly upregulated in toll-like receptor (TLR)-activated pDCs and was crucial for TLR7/9 ligand- or herpesvirus-induced production of IFN-α and IFN-λ by pDCs. miR-21-deficient pDCs produced significantly lower levels of IFN-α and IFN-λ on activation than those by wild-type pDCs. Impaired antiviral immune responses were also observed in miR-21-deficient mice. Mechanistically, we identified phosphatase and tensin homolog (PTEN) as the major target of miR-21 in pDCs, and miR-21 deficiency resulted in increased expression of PTEN that suppressed TLR-mediated activation of PI3K-Akt-mTOR signaling in pDCs. Hence, our findings provide evidence that miR-21 positively regulates both IFN-α and IFN-λ production and identify an important role for miR-21 in regulating the function of pDCs and in host antiviral immunity.

摘要

浆细胞样树突状细胞(pDCs)是I型和III型干扰素(IFNs)的主要生产者,在宿主抗病毒免疫中发挥着重要作用。微小RNA(miRs)是小的非编码RNA,可调节许多免疫过程。尽管对pDCs产生I型干扰素的分子调控已进行了广泛研究,但对III型干扰素产生的调控尚未得到充分研究,特别是在转录后水平。我们在此表明,miR-21是pDCs产生IFN-α和IFN-λ以及促进宿主抵抗病毒感染的必需正调节因子。miR-21在 toll样受体(TLR)激活的pDCs中显著上调,并且对于TLR7/9配体或疱疹病毒诱导的pDCs产生IFN-α和IFN-λ至关重要。与野生型pDCs相比,miR-21缺陷型pDCs在激活时产生的IFN-α和IFN-λ水平显著降低。在miR-21缺陷型小鼠中也观察到抗病毒免疫反应受损。从机制上讲,我们确定磷酸酶和张力蛋白同源物(PTEN)是pDCs中miR-21的主要靶标,miR-21缺陷导致PTEN表达增加,从而抑制pDCs中TLR介导的PI3K-Akt-mTOR信号通路的激活。因此,我们的研究结果提供了证据,表明miR-21正向调节IFN-α和IFN-λ的产生,并确定了miR-21在调节pDCs功能和宿主抗病毒免疫中的重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7965/5567078/59c48f2af710/fimmu-08-00947-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7965/5567078/3fd121459564/fimmu-08-00947-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7965/5567078/77b64e031e4c/fimmu-08-00947-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7965/5567078/314fd3622115/fimmu-08-00947-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7965/5567078/fcc3c91a442d/fimmu-08-00947-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7965/5567078/59c48f2af710/fimmu-08-00947-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7965/5567078/3fd121459564/fimmu-08-00947-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7965/5567078/77b64e031e4c/fimmu-08-00947-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7965/5567078/314fd3622115/fimmu-08-00947-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7965/5567078/fcc3c91a442d/fimmu-08-00947-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7965/5567078/59c48f2af710/fimmu-08-00947-g005.jpg

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