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An unconventional role for miRNA: let-7 activates Toll-like receptor 7 and causes neurodegeneration.miRNA 的非常规作用:let-7 激活 Toll 样受体 7 并导致神经退行性变。
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Protective and pathogenic functions of macrophage subsets.巨噬细胞亚群的保护和致病功能。
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Characterization of extracellular circulating microRNA.细胞外循环 microRNA 的特征。
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Targeting the ANG2/TIE2 axis inhibits tumor growth and metastasis by impairing angiogenesis and disabling rebounds of proangiogenic myeloid cells.靶向 ANG2/TIE2 轴通过抑制血管生成和使促血管生成的髓样细胞的反弹失活来抑制肿瘤生长和转移。
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Secreted monocytic miR-150 enhances targeted endothelial cell migration.分泌型单核细胞 miR-150 增强靶向性内皮细胞迁移。
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Increased miR-21 expression during human monocyte differentiation into DCs.人单核细胞分化为树突状细胞过程中miR-21表达增加。
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外泌体来源的微小RNA和细胞微小RNA激活先天免疫。

Exosome-derived miRNAs and cellular miRNAs activate innate immunity.

作者信息

Mobergslien Anne, Sioud Mouldy

机构信息

Institute for Cancer Research, Department of Immunology, Oslo University Hospital Radiumhospitalet, Oslo, Norway.

出版信息

J Innate Immun. 2014;6(1):105-10. doi: 10.1159/000351460. Epub 2013 Jun 14.

DOI:10.1159/000351460
PMID:23774807
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6741584/
Abstract

Circulating exosome-containing small RNAs have been demonstrated in vitro to be taken up by recipient cells and to alter gene expression through RNA interference. Here, we show that exosomes purified from various cancer cell lines as well as gel-purified exosomal and cellular miRNAs can induce pro-inflammatory cytokine expression in human peripheral blood mononuclear cells. Thus, circulating miRNAs may trigger innate immunity via pathogen recognition receptors, a new miRNA-activated pathway that merits some consideration.

摘要

体外实验已证实,循环中含外泌体的小RNA可被受体细胞摄取,并通过RNA干扰改变基因表达。在此,我们发现,从各种癌细胞系中纯化得到的外泌体以及凝胶纯化的外泌体和细胞miRNA,均可诱导人外周血单核细胞表达促炎细胞因子。因此,循环miRNA可能通过病原体识别受体触发先天免疫,这是一条值得关注的新的miRNA激活途径。