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多发性硬化症患者APOE和ACKR3基因的DNA甲基化变化及其与血液重金属水平的关系。

Changes in DNA methylation in APOE and ACKR3 genes in multiple sclerosis patients and the relationship with their heavy metal blood levels.

作者信息

Hasani Nourian Yazdan, Beh-Pajooh Abbas, Aliomrani Mehdi, Amini Mohsen, Sahraian Mohammad A, Hosseini Rohollah, Mohammadi Saeid, Ghahremani Mohammad H

机构信息

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Neurotoxicology. 2021 Dec;87:182-187. doi: 10.1016/j.neuro.2021.09.008. Epub 2021 Oct 6.

Abstract

Multiple sclerosis (MS) is a chronic inflammatory disease with demyelinated lesions in the central nervous system caused by genetic and environmental factors. DNA methylation as an epigenetic change influenced by environmental factors, including heavy metals has been implemented in MS disease. We investigated the correlation of DNA methylation changes in APOE and ACKR3 genes in MS patients and the possible association with blood concentration of arsenic (As), cadmium (Cd) and lead (Pb) as major heavy metal pollutants. This study included 69 relapsing-remitting multiple sclerosis (RR-MS) patients and 69 age/gender-matched healthy subjects. The HRM real-time PCR method was used to investigate the changes in DNA methylation and heavy metal concentrations were measured by electrothermal atomic absorption spectrometry. Our results showed that the methylation pattern in the ACKR3 gene of the patient group was more hypomethylated, while in the case of the APOE gene, this pattern was more towards hypermethylation compared to healthy subjects. Moreover, the blood levels of As and Cd metals, but not Pb, were significantly higher in the patient group compare to the control group (p ≤ 0.05). The data indicate that the increase in expression of ACKR3 gene by hypomethylation and the decrease in expression of APOE gene via hypermethylation are possibly involved in the onset and progression of inflammatory processes in MS patients. The level of As can also lead to hypomethylation by disrupting the methylation patterns of the ACKR3 gene, resulting in increased expression in MS patients. Finally, we have shown that epigenetic changes can be an important factor in increasing and decreasing the expression of genes involved in the onset and/or progression of inflammatory processes in MS. Furthermore, exposure to heavy metals, especially As, by changing the natural patterns of DNA methylation can be effective in this disease.

摘要

多发性硬化症(MS)是一种慢性炎症性疾病,由遗传和环境因素导致中枢神经系统出现脱髓鞘病变。DNA甲基化作为一种受环境因素(包括重金属)影响的表观遗传变化,已在MS疾病中得到研究。我们调查了MS患者中APOE和ACKR3基因DNA甲基化变化的相关性,以及与主要重金属污染物砷(As)、镉(Cd)和铅(Pb)血浓度的可能关联。本研究纳入了69例复发缓解型多发性硬化症(RR-MS)患者和69例年龄/性别匹配的健康受试者。采用高分辨率熔解曲线实时荧光定量PCR法研究DNA甲基化变化,并用电热原子吸收光谱法测量重金属浓度。我们的结果显示,与健康受试者相比,患者组ACKR3基因的甲基化模式更多为低甲基化,而APOE基因则更多趋于高甲基化。此外,与对照组相比,患者组血液中As和Cd金属水平显著更高,但Pb水平无显著差异(p≤0.05)。数据表明,ACKR3基因通过低甲基化导致表达增加,APOE基因通过高甲基化导致表达降低,可能参与了MS患者炎症过程的发生和发展。As水平也可能通过破坏ACKR3基因的甲基化模式导致低甲基化,从而使MS患者的表达增加。最后,我们表明表观遗传变化可能是增加和减少参与MS炎症过程发生和/或发展的基因表达的重要因素。此外,接触重金属,尤其是As,通过改变DNA甲基化的自然模式,可能在这种疾病中发挥作用。

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