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与生物活性玻璃接触培养的中度分化成骨细胞样细胞的行为

Behaviour of moderately differentiated osteoblast-like cells cultured in contact with bioactive glasses.

作者信息

Hattar S, Berdal A, Asselin A, Loty S, Greenspan D C, Sautier J-M

机构信息

Laboratoire de Biologie Orofaciale et Pathologie, INSERM EMI-U 0110, Institut Biomédical des Cordeliers, Esc. E-2è étage, 15-21 rue de l'Ecole de Médecine, F-75270 Paris Cedex 06, France.

出版信息

Eur Cell Mater. 2002 Dec 31;4:61-9. doi: 10.22203/ecm.v004a05.

Abstract

Bioactive glasses have been shown to stimulate osteogenesis both in vivo and in vitro. However, the molecular mechanisms underlying this process are still poorly understood. In this study, we have investigated the behaviour of osteoblast-like cells (MG63), cultured in the presence of bioglass particles. Three types of granules were used: 45S5 bioactive glass, 45S5 granules preincubated in tris buffer and 60S non-reactive glass, used as control. Phase contrast microscopy permitted step-by-step visualization of cell cultures in contact with the particles. Ultrastructural observations of undecalcified sections revealed direct contacts of the cells and an electron-dense layer located at the periphery of the material. Protein synthesis was evaluated biochemically and showed a gradual increase throughout the culture time in the three types of cultures. Alkaline phosphatase was detected in situ, in clusters of packed cells either in contact with the material or in the background cell layer. Semi-quantitative RT-PCR analysis of the main osteoblastic markers showed that gene expression was maintained in all three cultures. The fact that osteocalcin was not detected, supports the fact that the MG63 cell line is composed of less differentiated osteogenic cells rather than mature osteoblasts. We also demonstrated for the first time in this cell line, the expression of Msx-2, Dlx-3 and Dlx-7 homeogenes, known to regulate in vivo foetal skeletogenesis as well as adult skeletal regeneration. However, no significant differences could be recognised in the expression pattern of bone markers between the three types of cultures. Yet these preliminary results indicate that bioactive glasses provided a suitable environment for the growth and proliferation of osteoblasts in vitro, since no drastic changes in phenotype expression of pre-osteoblasts was noted.

摘要

生物活性玻璃已被证明在体内和体外均能刺激骨生成。然而,这一过程背后的分子机制仍知之甚少。在本研究中,我们研究了在生物玻璃颗粒存在下培养的成骨样细胞(MG63)的行为。使用了三种类型的颗粒:45S5生物活性玻璃、在三羟甲基氨基甲烷缓冲液中预孵育的45S5颗粒以及用作对照的60S非活性玻璃。相差显微镜允许逐步观察与颗粒接触的细胞培养物。未脱钙切片的超微结构观察揭示了细胞与位于材料周边的电子致密层的直接接触。通过生化方法评估蛋白质合成,结果显示在三种类型的培养物中,整个培养期间蛋白质合成逐渐增加。在与材料接触的密集细胞簇或背景细胞层中,原位检测到碱性磷酸酶。对主要成骨细胞标志物的半定量逆转录-聚合酶链反应分析表明,所有三种培养物中的基因表达均得以维持。未检测到骨钙素这一事实支持了MG63细胞系由分化程度较低的成骨细胞而非成熟成骨细胞组成这一观点。我们还首次在该细胞系中证明了Msx-2、Dlx-3和Dlx-7同源基因的表达,已知这些基因在体内调节胎儿骨骼生成以及成人骨骼再生。然而,在三种类型的培养物之间,骨标志物的表达模式未发现显著差异。不过,这些初步结果表明,生物活性玻璃为成骨细胞在体外的生长和增殖提供了适宜的环境,因为未观察到前成骨细胞表型表达的剧烈变化。

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