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HOTAIR 而非 ANRIL 长非编码 RNA 有助于多发性硬化症的发病机制。

HOTAIR but not ANRIL long non-coding RNA contributes to the pathogenesis of multiple sclerosis.

机构信息

Faculty of Biological Sciences, Department of Genetics, Tarbiat Modares University, Tehran, Iran.

Faculty of Medicine, Department of Medical Biotechnology & Molecular Sciences, North Khorasan University of Medical Sciences, Bojnurd, Iran.

出版信息

Immunology. 2018 Apr;153(4):479-487. doi: 10.1111/imm.12850. Epub 2017 Nov 16.

Abstract

Studies have revealed that dysregulation in gene expression is one of the main aspects of multiple sclerosis (MS) pathogenesis. Although the molecular pathways underlying the immunomodulatory role of vitamin D (VD) in MS is not completely elucidated, VD has more recently become a topic of interest in immune regulation and is widely administered to patients with MS as an immunomodulatory supplement. Long non-coding RNAs (lncRNAs) are known to play important roles in regulation of gene expression via different mechanisms. Given that VD-related genes are regulated by epigenetic mechanisms, here we aimed to evaluate the role of VD in combination with HOTAIR and ANRIL lncRNAs using in vivo, in vitro and in silico experiments in MS pathogenesis. Our data revealed that HOTAIR but not ANRIL lncRNA is probably involved in the pathogenesis of MS and experimental autoimmune encephalomyelitis through an unclear mechanism and it seems that by affecting the expression, inflammation and VD can influence HOTAIR-related mechanisms, which require further study.

摘要

研究表明,基因表达失调是多发性硬化症(MS)发病机制的主要方面之一。尽管维生素 D(VD)在 MS 中的免疫调节作用的分子途径尚未完全阐明,但 VD 最近已成为免疫调节的研究热点,并广泛应用于 MS 患者作为免疫调节剂。长链非编码 RNA(lncRNA)通过不同的机制已知在基因表达调控中发挥重要作用。鉴于 VD 相关基因受表观遗传机制调控,因此我们旨在使用体内、体外和计算机实验来评估 VD 在 MS 发病机制中与 HOTAIR 和 ANRIL lncRNA 的联合作用。我们的数据表明,HOTAIR 而非 ANRIL lncRNA 可能通过一种不明机制参与 MS 和实验性自身免疫性脑脊髓炎的发病机制,似乎通过影响表达、炎症和 VD 可以影响 HOTAIR 相关机制,这需要进一步研究。

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