血清外泌体miR-128-2-5p对COL6A2表达和绝经后骨质疏松的调节作用。

IF 3.1 2区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Liangjie Lu, Lijun Wang, Huihan Wang, Minjie Yang
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引用次数: 0

摘要

本研究探讨了血清源性外泌体(Exos)中miR-128-2-5p对COL6A2表达的影响及其在绝经后骨质疏松症(POMP)中的意义。利用生物信息学分析,我们确定了1317个差异表达基因(DEGs),主要富集于局灶粘附途径(成骨细胞粘附的关键调节因子)。一个重要的基因COL6A2在POMP中出现显著下调,具有作为诊断标记的潜力。预测分析将上游miRNA miR-128-2-5p与COL6A2的调控联系起来,miR-128-2-5p在Exos中高度富集。实验中,POMP患者的Exos显示miR-128-2-5p水平升高,这在体外抑制COL6A2的表达,减少成骨细胞粘附并加剧骨质疏松症。这些发现强调了外泌体miR-128-2-5p在骨代谢中的关键作用,提示了POMP的一种新的分子机制和潜在的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulatory role of miR-128-2-5p in serum exosomes on COL6A2 expression and postmenopausal osteoporosis.

This study investigates the influence of miR-128-2-5p within serum-derived exosomes (Exos) on COL6A2 expression and its implications in postmenopausal osteoporosis (POMP). Utilizing bioinformatics analysis, we identified 1317 differentially expressed genes (DEGs), primarily enriched in the focal adhesion pathway-a critical regulator of osteoblast adhesion. A significant gene, COL6A2, emerged as notably downregulated in POMP, possessing potential as a diagnostic marker. Predictive analysis linked the upstream miRNA miR-128-2-5p, highly enriched in Exos, with the regulation of COL6A2. Experimentally, Exos from POMP patients demonstrated elevated miR-128-2-5p levels, which inhibited COL6A2 expression in vitro, reducing osteoblast adhesion and exacerbating osteoporotic conditions. These findings highlight the pivotal role of exosomal miR-128-2-5p in bone metabolism, suggesting a novel molecular mechanism and a potential therapeutic target in POMP.

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来源期刊
Human molecular genetics
Human molecular genetics 生物-生化与分子生物学
CiteScore
6.90
自引率
2.90%
发文量
294
审稿时长
2-4 weeks
期刊介绍: Human Molecular Genetics concentrates on full-length research papers covering a wide range of topics in all aspects of human molecular genetics. These include: the molecular basis of human genetic disease developmental genetics cancer genetics neurogenetics chromosome and genome structure and function therapy of genetic disease stem cells in human genetic disease and therapy, including the application of iPS cells genome-wide association studies mouse and other models of human diseases functional genomics computational genomics In addition, the journal also publishes research on other model systems for the analysis of genes, especially when there is an obvious relevance to human genetics.
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