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微小RNA在多发性硬化症中的表达、调控及功能

Expression, regulation and function of microRNAs in multiple sclerosis.

作者信息

Ma Xinting, Zhou Juhua, Zhong Yin, Jiang Linlin, Mu Ping, Li Yanmin, Singh Narendra, Nagarkatti Mitzi, Nagarkatti Prakash

机构信息

1. Institute for Tumor Immunology, Ludong University College of Life Sciences, 186 Hongqi Middle Road, Yantai, Shandong 264025, China.

2. Department of Pathology, Microbiology and Immunology, School of Medicine, University of South Carolina, 6439 Garners Ferry Road, Columbia, SC 29209, USA.

出版信息

Int J Med Sci. 2014 Jun 2;11(8):810-8. doi: 10.7150/ijms.8647. eCollection 2014.

Abstract

MicroRNAs (miRNAs) are single-stranded 19-25 nucleotide-long RNAs and have an important role in post-transcriptional gene silencing. It has been demonstrated that miRNAs are dysregulated in patients with multiple sclerosis (MS). For instance, miR-21, miR-142-3p, miR-146a, miR-146b, miR-155 and miR-326 were up-regulated in both peripheral blood mononuclear cells (PBMCs) and brain white matter lesions from MS patients and mouse model as well. These up-regulated miRNAs may be used as a signature for MS and play critical roles in MS pathogenesis. Moreover, miR-15a, miR-19a, miR-22, miR-210 and miR-223 were up-regulated in both regulatory T cells (Tregs) and other samples such as plasma, blood cells, PBMCs and brain white matter tissues from MS patients, suggesting that these up-regulated miRNAs and Tregs may also play a role in MS pathogenesis. Contrarily, other miRNAs such as miR-15a, miR-15b, miR-181c and miR-328 were down-regulated in MS. Drugs such as interferon-β and glatiramer acetate for MS treatment may regulate miRNA expression and thus have benefits for MS patients. The dysregulated miRNAs such as miR-155 and miR-326 may be used as diagnostic markers and therapeutic targets for MS.

摘要

微小RNA(miRNA)是长度为19 - 25个核苷酸的单链RNA,在转录后基因沉默中发挥重要作用。已有研究表明,微小RNA在多发性硬化症(MS)患者中表达失调。例如,miR - 21、miR - 142 - 3p、miR - 146a、miR - 146b、miR - 155和miR - 326在MS患者和小鼠模型的外周血单个核细胞(PBMC)以及脑白质病变中均上调。这些上调的微小RNA可能作为MS的一种特征,并在MS发病机制中起关键作用。此外,miR - 15a、miR - 19a、miR - 22、miR - 210和miR - 223在MS患者的调节性T细胞(Tregs)以及血浆、血细胞、PBMC和脑白质组织等其他样本中均上调,表明这些上调的微小RNA和Tregs可能也在MS发病机制中发挥作用。相反,其他微小RNA如miR - 15a、miR - 15b、miR - 181c和miR - 328在MS中下调。用于MS治疗的药物如干扰素-β和醋酸格拉替雷可能调节微小RNA的表达,从而对MS患者有益。失调的微小RNA如miR - 155和miR - 326可作为MS的诊断标志物和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eac6/4057480/74412f75cbd7/ijmsv11p0810g001.jpg

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