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MicroRNAs-系统性红斑狼疮发病机制的新型调节因子。

MicroRNAs--novel regulators of systemic lupus erythematosus pathogenesis.

机构信息

Joint Molecular Rheumatology Laboratory of the Institute of Health Sciences and Shanghai Renji Hospital, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai Jiaotong University School of Medicine, 145 Shan Dong Middle Road, Shanghai 200001, China.

出版信息

Nat Rev Rheumatol. 2012 Dec;8(12):701-9. doi: 10.1038/nrrheum.2012.142. Epub 2012 Oct 16.

DOI:10.1038/nrrheum.2012.142
PMID:23070646
Abstract

Dysregulation of gene expression can cause complex disease phenotypes. MicroRNAs (miRNAs) are well known to fine-tune cellular gene expression to control immune cell development and regulate adaptive and innate immune responses. Discoveries over the past decade have indicated that aberrant expression of miRNAs is associated with the pathogenesis of multiple immunological diseases, including systemic lupus erythematosus (SLE). Indeed, profiling miRNA expression in blood cells, body fluid and target tissues taken from patients with SLE has revealed unique miRNA signatures when compared with healthy individuals or those with other diseases. Moreover, dysregulation of these miRNAs has also been found to be associated with disease activity and major organ involvement. In our opinion, therefore, miRNAs have the potential to act as biomarkers for the diagnosis and assessment of patients with SLE. This Review provides an overview of the novel cellular and molecular mechanisms that seem to underlie the roles of miRNAs in SLE disease processes, as well as the future therapeutic potential of targeting miRNAs in the management of patients with SLE.

摘要

基因表达失调可导致复杂的疾病表型。众所周知,微小 RNA(miRNA)可精细调节细胞基因表达,以控制免疫细胞的发育,并调节适应性和固有免疫反应。过去十年的研究发现,miRNA 的异常表达与多种免疫性疾病的发病机制有关,包括系统性红斑狼疮(systemic lupus erythematosus,SLE)。事实上,与健康个体或其他疾病患者相比,对来自 SLE 患者的血细胞、体液和靶组织中的 miRNA 表达进行分析后,揭示了独特的 miRNA 特征。此外,这些 miRNA 的失调也与疾病活动度和主要器官受累有关。因此,我们认为 miRNA 有可能作为 SLE 患者的诊断和评估的生物标志物。本文综述了 miRNA 在 SLE 疾病过程中发挥作用的新的细胞和分子机制,以及针对 miRNA 进行靶向治疗 SLE 患者的未来治疗潜力。

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本文引用的文献

1
Genetic susceptibility to lupus: the biological basis of genetic risk found in B cell signaling pathways.狼疮的遗传易感性:B 细胞信号通路中发现的遗传风险的生物学基础。
J Leukoc Biol. 2012 Sep;92(3):577-91. doi: 10.1189/jlb.0212095. Epub 2012 Jun 29.
2
Identification of microRNA-31 as a novel regulator contributing to impaired interleukin-2 production in T cells from patients with systemic lupus erythematosus.鉴定微小RNA-31作为一种新型调节因子,其导致系统性红斑狼疮患者T细胞中白细胞介素-2产生受损。
Arthritis Rheum. 2012 Nov;64(11):3715-25. doi: 10.1002/art.34596.
3
The microRNA miR-23b suppresses IL-17-associated autoimmune inflammation by targeting TAB2, TAB3 and IKK-α.
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Arq Bras Cardiol. 2023 Aug 4;120(7):e20230303. doi: 10.36660/abc.20230303.
4
Deletion of microRNA-183-96-182 Cluster in Lymphocytes Suppresses Anti-DsDNA Autoantibody Production and IgG Deposition in the Kidneys in C57BL/6-Fas Mice.淋巴细胞中微小RNA - 183 - 96 - 182簇的缺失抑制C57BL/6 - Fas小鼠抗双链DNA自身抗体的产生及肾脏中IgG的沉积。
Front Genet. 2022 Jul 7;13:840060. doi: 10.3389/fgene.2022.840060. eCollection 2022.
5
MiR-30a-centered molecular crosstalk regulates Th17 differentiation.以miR-30a为中心的分子串扰调节辅助性T细胞17分化。
Cell Mol Immunol. 2022 Aug;19(8):960-961. doi: 10.1038/s41423-022-00888-9. Epub 2022 Jun 23.
6
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