Linoleic acid promotes osteogenic differentiation of bone marrow mesenchymal stem cells and ameliorates ovariectomy (OVX)-induced osteoporosis in mice through the PI3K/AKT pathway

IF 2.8 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Hao Liao , Xiangping Luo , Liqin Jiang
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引用次数: 0

Abstract

Bone mineral density (BMD) reduction is heavily involved in osteoporosis. Bone marrow mesenchymal stem cells (BMSCs) are promising candidates in the implantation treatment of bone loss-related diseases. Traditional Chinese herbs and their active components are effective in osteoporosis therapy. The effects of linoleic acid on osteogenesis and osteoporosis have been investigated in this study, revealing multifaceted findings through several analyses and experiments. A total of 41 overlapping disease-drug target genes were obtained between differentially expressed genes in osteoporosis and linoleic acid potential targets. Linoleic acid was shown to enhance BMSC osteogenic differentiation and mineralization in in vitro assays. Additionally, linoleic acid significantly countered bone loss and improved bone microstructure in a mouse model of osteoporosis induced by ovarian varixectomy (OVX) operation. Molecular docking was used to predict the interaction between linoleic acid and the top ten Hub genes. The predicted binding energy of Retinoid X Receptor Alpha (RXRA) is the lowest. Moreover, linoleic acid stimulation increased the expression of RXRA in BMSCs. Functional enrichment and pathway analysis of the overlapping potential targets highlighted their involvement in crucial biological processes and signaling pathways, including the PI3K-AKT signaling. Linoleic acid promoted the phosphorylation of PI3K and AKT. Lastly, the siRNA for RXRA knockdown and PI3K/AKT inhibitor LY294002 exerted opposite effects on BMSCs to linoleic acid, and significantly attenuated the effects of linoleic acid on BMSC osteogenic differentiation and the PI3K/AKT signaling activation, suggesting that the functions of linoleic acid might be mediated by the PI3K/AKT signaling. Moreover, linoleic acid also inhibited osteoclastogenetic differentiation. Conclusively, linoleic acid, the main active compound of Rehmanniae Radix Praeparata (RR), could promote BMSC osteogenic differentiation by enhancing the PI3K/AKT signaling activation.
亚油酸通过PI3K/AKT通路促进骨髓间充质干细胞成骨分化并改善卵巢切除术(OVX)诱导的小鼠骨质疏松症。
骨密度(BMD)降低与骨质疏松症密切相关。骨髓间充质干细胞(BMSCs)在骨丢失相关疾病的植入治疗中具有广阔的应用前景。中药及其有效成分是治疗骨质疏松症的有效药物。本研究探讨了亚油酸对成骨和骨质疏松症的影响,通过多项分析和实验揭示了多方面的发现。在骨质疏松症差异表达基因和亚油酸潜在靶点之间共获得41个重叠的疾病药物靶基因。在体外实验中,亚油酸被证明能促进骨髓间充质干细胞成骨分化和矿化。此外,在卵巢静脉曲张切除术(OVX)引起的骨质疏松小鼠模型中,亚油酸可显著对抗骨质流失并改善骨微观结构。利用分子对接预测亚油酸与前10个Hub基因的相互作用。类视黄醇X受体α (RXRA)的预测结合能最低。此外,亚油酸刺激可增加骨髓间充质干细胞中RXRA的表达。重叠潜在靶点的功能富集和通路分析强调了它们参与关键的生物过程和信号通路,包括PI3K-AKT信号通路。亚油酸促进PI3K和AKT的磷酸化。最后,RXRA敲低siRNA和PI3K/AKT抑制剂LY294002对骨髓间充质干细胞的作用与亚油酸相反,显著减弱亚油酸对骨髓间充质干细胞成骨分化和PI3K/AKT信号激活的作用,提示亚油酸的功能可能是由PI3K/AKT信号介导的。此外,亚油酸还能抑制破骨细胞的分化。综上所述,生地黄(RR)的主要活性化合物亚油酸可能通过增强PI3K/AKT信号的激活来促进BMSC成骨分化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.10
自引率
0.00%
发文量
124
审稿时长
19 days
期刊介绍: IJBCB publishes original research articles, invited reviews and in-focus articles in all areas of cell and molecular biology and biomedical research. Topics of interest include, but are not limited to: -Mechanistic studies of cells, cell organelles, sub-cellular molecular pathways and metabolism -Novel insights into disease pathogenesis -Nanotechnology with implication to biological and medical processes -Genomics and bioinformatics
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