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Comparison between curcumin and all-trans retinoic acid in the osteogenic differentiation of mouse bone marrow mesenchymal stem cells

机译:姜黄素与全反式维甲酸在小鼠骨髓间充质干细胞成骨分化中的比较

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摘要

The use of bone marrow mesenchymal stem cells (BMSCs) has great potential in cell therapy, particularly in the orthopedic field. BMSCs represent a valuable renewable cell source that have been successfully utilized to treat damaged skeletal tissue and bone defects. BMSCs can be induced to differentiate into osteogenic lineages via the addition of inducers to the growth medium. The present study examined the effects of all-trans retinoic acid (ATRA) and curcumin on the osteogenic differentiation of mouse BMSCs. Morphological changes, the expression levels of the bone-associated gene markers bone morphogenetic protein 2, runt-related transcription factor and osterix during differentiation, an in vitro mineralization assay, and changes in osteocalcin expression revealed that curcumin supplementation promoted the osteogenic differentiation of BMSCs. By contrast, the application of ATRA increased osteogenic differentiation during the early stages, but during the later stages, it decreased the mineralization of differentiated cells. In addition, to the best of our knowledge, the present study is the first to examine the effect of curcumin on the osteogenic potency of mouse embryonic fibroblasts (MEFs) after reprogramming with human lim mineralization protein (hLMP-3), which is a positive osteogenic regulator. The results revealed that curcumin-supplemented culture medium increased hLMP-3 osteogenic potency compared with that of MEFs cultured in the non-supplemented medium. The present results demonstrate that enrichment of the osteogenic culture medium with curcumin, a natural osteogenic inducer, increased the osteogenic differentiation capacity of BMSCs as well as that of MEFs reprogrammed with hLMP-3.
机译:骨髓间充质干细胞(BMSCs)的使用在细胞治疗中具有巨大潜力,尤其是在整形外科领域。 BMSCs是一种有价值的可再生细胞来源,已成功地用于治疗受损的骨骼组织和骨缺损。通过向生长培养基中添加诱导剂,可以诱导BMSC分化为成骨细胞系。本研究检查了全反式维甲酸(ATRA)和姜黄素对小鼠骨髓间充质干细胞成骨分化的影响。形态变化,骨相关基因标志物骨形态发生蛋白2,矮子相关转录因子和osterix在分化过程中的表达水平,体外矿化测定以及骨钙素表达的变化表明姜黄素的添加促进了BMSCs的成骨分化。相比之下,ATRA的应用在早期增加了成骨分化,但在后期却减少了分化细胞的矿化作用。另外,据我们所知,本研究是第一个研究姜黄素对人胚矿化蛋白(hLMP-3)重编程后对小鼠胚胎成纤维细胞(MEF)成骨能力的影响的研究成骨调节剂。结果表明,与在非补充培养基中培养的MEF相比,补充姜黄素的培养基增加了hLMP-3的成骨能力。目前的结果表明,用天然的成骨诱导剂姜黄素富集成骨培养基可以增加BMSCs和用hLMP-3重新编程的MEF的成骨分化能力。

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