衰老和全身激素状态影响循环miR-21、miR-146a和FasL水平

R. Kangas, E. Pöllänen, V. Kovanen
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引用次数: 0

摘要

microrna是一种小分子,存在于所有细胞类型和体液中,最常见的是通过翻译抑制对基因表达产生负面影响。它们在各种生理状况和疾病中的作用在过去二十年中得到了强调。在我们最近对绝经后的同卵双胞胎姐妹(n=11)的研究中,我们研究了不同的全身激素状态如何影响与炎症和凋亡相关的特定循环microrna和其他分子的水平,这两个过程都与衰老有关。我们的研究结果表明,绝经后使用雌激素激素替代(HRT)的妇女体内的miR-21、miR-146a和Fas配体水平低于未使用同卵双胞胎的妇女(p=0.018、p=0.039、p=0.021)。为了加强衰老效应,我们还测量了具有自然激素状态的绝经前对照女性(n=8)的相同标志物,发现年轻女性的炎症谱更健康,血清miR-21谱与HRT使用者比非使用者更相似,miR-146和FasL谱与非HRT使用者更相似。这些发现表明HRT对循环炎症相关调节分子有影响。我们是否可以明确地说这些影响是积极的还是消极的,需要进一步的调查和对监管体系的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aging and systemic hormonal status affects the circulating miR-21, miR-146a and FasL levels
MicroRNAs are small  molecules, found in all cell types and body fluids, which most commonly affect negatively to gene expressions by translational repression. Their role in various physiological conditions and diseases has been emphasized during the last twenty years. In our recent studies with postmenopausal monozygotic twin sisters (n=11), we have investigated how different systemic hormonal status affects the levels of specific circulating microRNAs and other molecules related to inflammation and apoptosis, both processes associated with aging. Our results have shown that the systemic levels of miR-21, miR-146a and Fas ligand are lower within the postmenopausal women who are using estrogen-based hormonal replacement (HRT), compared to their non-using co-twins (p=0.018, p=0.039, p=0.021, respectively). To strengthen the aging effect, we also measured the same markers from the premenopausal control women (n=8), with natural hormonal status, and found out that the inflammatory profile was healthier among the young women and that the serum miR-21 profile was more similar with the HRT users than non-users, and miR-146 and FasL profile more similar to non-users. These findings demonstrate that HRT has effects on the circulating inflammation related regulatory molecules. Whether we can state that the effects are clearly positive or negative, needs further investigations and understanding of the regulatory system.
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