首页> 外文期刊>In Vitro Cellular and Developmental Biology. Animal: Journal of the Tissues Culture Association >Effects of FGF2 and FGF9 on osteogenic differentiation of bone marrow-derived progenitors
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Effects of FGF2 and FGF9 on osteogenic differentiation of bone marrow-derived progenitors

机译:FGF2和FGF9对骨髓祖细胞成骨分化的影响

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Bone repair is a major concern in reconstructive surgery. Transplants containing osteogenically committed mesenchymal stem cells (MSCs) provide an alternative source to the currently used autologous bone transplants which have limited supply and require additional surgery to the patient. A major drawback, however is the lack of a critical mass of cells needed for successful transplantation. The purpose of the present study was to test the effects of FGF2 and FGF9 on expansion and differentiation of MSCs in order to establish an optimal culture protocol resulting in sufficient committed osteogenic cells required for successful in vivo transplantation. Bone marrow-derived MSCs cultured in alpha MEM medium supplemented with osteogenic supplements for up to three passages (control medium), were additionally treated with FGF2 and FGF9 in various combinations. Cultures were evaluated for viability, calcium deposition and in vivo osteogenic capacity by testing subcutaneous transplants in nude mice. FGF2 had a positive effect on the proliferative capacity of cultured MSCs compared to FGF9 and control medium treated cultures. Cultures treated with FGF2 followed by FGF9 showed an increased amount of extracted Alizarin red indicating greater osteogenic differentiation. Moreover, the osteogenic capacity of cultured cells transplanted in immunodeficient mice revealed that cells that were subjected to treatment with FGF2 in the first two passages and subsequently to FGF9 in the last passage only, were more successful in forming new bone. It is concluded that the protocol using FGF2 prior to FGF9 is beneficial to cell expansion and commitment, resulting in higher in vivo bone formation for successful bone tissue engineering.
机译:骨修复是重建手术中的主要问题。包含骨源性间充质干细胞(MSC)的移植物为目前使用的自体骨移植物提供了替代来源,后者的供应量有限并且需要对患者进行额外的手术。然而,主要缺点是缺乏成功移植所需的临界细胞量。本研究的目的是测试FGF2和FGF9对MSC扩增和分化的影响,以建立最佳培养方案,从而产生成功进行体内移植所需的足够定型成骨细胞。在补充了成骨性补充剂的alpha MEM培养基中培养的骨髓来源的MSC最多可传三代(对照培养基),还以各种组合用FGF2和FGF9处理。通过在裸鼠中测试皮下移植物,评估培养物的生存力,钙沉积和体内成骨能力。与FGF9和对照培养基处理的培养物相比,FGF2对培养的MSC的增殖能力具有积极作用。用FGF2和FGF9处理的培养物显示出更高的提取茜素红数量,表明其成骨能力更高。此外,在免疫缺陷小鼠中移植的培养细胞的成骨能力表明,在前两代中仅接受FGF2处理,仅在最后一代中仅接受FGF9处理的细胞,在形成新骨方面更为成功。结论是,在FGF9之前使用FGF2的方案有益于细胞扩增和定型,从而导致更高的体内骨形成,从而成功进行骨组织工程设计。

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