微RNA 135-5P和p62之间的潜在关联及其对多发性硬化症NRF2通路的影响
Azza Abusree Ahmed1, Salwa Fayez Hasan1, Laila Ahmed Rashed1
1Medical Biochemistry and Molecular Biology Department, Unit of Biochemistry and Molecular Biology, Faculty of Medicine, Cairo University, Cairo, Egypt.
Reports of biochemistry & molecular biology
|August 1, 2024
概括
这项研究在多发性硬化症 (MS) 患者中发现了较低水平的核因子红色素2相关因子2 (NRF2) 和p62. 微RNA135-5p,NF-κB和p53的升高表明它们通过NRF2通路参与MS的发病.
科学领域:
- 神经免疫学 神经免疫学
- 分子生物学分子生物学
- 生物化学 生物化学
背景情况:
- 多发性硬化症 (MS) 是一种具有复杂病源性的致残性神经疾病.
- 核因子红色素2相关因子2 (NRF2) 调节抗氧化和抗炎反应.
- p62作为影响NRF2活性和自的支架蛋白.
研究的目的:
- 研究MS中微RNA 135-5p和p62之间的关联.
- 探索它们通过MS的NRF2通路对炎症和氧化应激的影响.
主要方法:
- 分析了来自60名多发性硬化患者和30名健康对照者的血清样本.
- 实时PCR被用于量化Nrf2,p62,miRNA135-5P和NF-κB.
- 使用ELISA测量p53的水平.
主要成果:
- 在MS患者中,Nrf2和p62表达显著下调.
- 在MS患者中,miRNA135-5P,NF-κB表达和p53水平显著升高.
- 确定了miRNA 135-5p和p62在MS病变发生过程中的潜在联系.
结论:
- miRNA 135-5p和p62可能在多发性硬化症的发病过程中发挥作用.
- 这些分子可能会通过NRF2通路影响炎症和氧化应激.
- 在MS中,NF-κB和p53可能会调解miRNA 135-5p和p62的影响.
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