[骨关节炎与衰老相互关系的表观遗传学机制]

Q4 Medicine
R N Mustafin
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引用次数: 0

摘要

根据这一假设,衰老过程中逆转录酶的激活会引起人体的免疫反应,从而诱发骨关节炎。诱发因素是与骨关节炎有关的多态性,这些多态性位于转座元件所在的内含子区和基因间区。在发炎的关节中,许多基因的表达都会发生变化,这可能是由于逆转录子的病理激活影响了基因组的表观遗传失调。为了证实这一假设,本文提供的数据显示,骨关节炎患者的血细胞中检测到激活的逆转录酶LINE1、ERV3、HERV-K18,关节组织中检测到内源性逆转录酶HERV-E2和HERV-WE1的表达产物以及组蛋白去乙酰化酶Sirt6活性的降低。通过对 MDTE 数据库和科学文献的分析,发现了 12 个源自 LINE 的 microRNA、5 个源自 SINE 的 microRNA 和 2 个源自 HERV 的 microRNA,它们会影响骨关节炎的发病机制并参与衰老机制,这可能会支持所提出的假说。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Epigenetic mechanisms of the interrelations of osteoarthritis with aging.]

A hypothesis is presented according to which the activation of retroelements during aging, causing immune reactions in the human body, is a trigger for the development of osteoarthritis. Predisposition factors for this are polymorphisms associated with osteoarthritis, located in intronic and intergenic regions where transposable elements are localized. In inflamed joints, changes in the expression of many genes are determined, which may be due to pathological activation of retroelements that influence epigenetic dysregulation of the genome. To confirm the hypothesis, data are presented that in patients with osteoarthritis, activated retroelements LINE1, ERV3, HERV-K18 are detected in blood cells, expression products of endogenous retroviruses HERV-E2 and HERV-WE1 and a decrease in the activity of histone deacetylase Sirt6 are detected in joint tissues. Analysis of the MDTE database and scientific literature revealed 12 microRNAs derived from LINE, 5 derived from SINE, 2 derived from HERV, affecting the pathogenesis of osteoarthritis and involved in the mechanisms of aging, which may indicate in favor of the presented hypothesis.

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CiteScore
0.50
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发文量
131
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