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首页> 外文期刊>Clinical and experimental pharmacology & physiology >DETAILED EXAMINATION OF CARTILAGE FORMATION and ENDOCHONDRAL OSSIFICATION USING HUMAN MESENCHYMAL STEM CELLS.
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DETAILED EXAMINATION OF CARTILAGE FORMATION and ENDOCHONDRAL OSSIFICATION USING HUMAN MESENCHYMAL STEM CELLS.

机译:使用人间充质干细胞详细检查软骨形成和软骨内骨化。

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摘要

1. Cartilage formation is one of the most complex processes in biology. The aim of the present study was to produce a simplified in vitro system to resolve its complexities. 2. Human mesenchymal stem cells (hMSC) were maintained in alginate beads with a chondrogenesis-induction medium containing 10 ng/mL transforming growth factor (TGF)-beta3. 3. At days 0, 2, 4, 8, 12, 16 and 19 of culture, we examined the cells using a light microscope and a transmission electron microscope. We also evaluated the cells using immunocryo-ultramicrotomy. 4. The present study demonstrated that hMSC produced numerous extracellular matrices containing abnormal collagen fibres following their exposure to a chondrogenesis-induction medium in alginate beads. At this time, calcification was detected by alizarin red staining and electron-dense particles, composed of hydroxyapatite, appeared in both the cytoplasm and the extracellular spaces. 5. In addition immunocryo-ultramicrotomy revealed that collagen type II, type X and proteoglycan were prominent and that osteocalcin was detectable at day 2. During 8-16 days of culture, collagen type X maintained its strong expression and the expression of osteocalcin increased markedly. In contrast, the expression of collagen type II and proteoglycan decreased with time. 6. These findings demonstrate that hMSC rapidly differentiate into chondrocytes expressing collagen type II and proteoglycan. 7. The expression of collagen type II and proteoglycan then dropped and the activity of collagen type X was the same as before (4-8 days). As a result, the cells developed into the next cell type, so-called hypertrophic chondrocytes. Finally, both osteocalcin activity and the calcification of cell bodies and extracellular matrices became evident, indicating endochondral ossification. Thus, we conclude that hMSC rapidly differentiate into chondrocytes, followed by the development of hypertrophic chondrocytes. Endochondral ossification is the final form in this culture. 8. The findings of the present study indicate that our three-dimensional culture is a convenient in vitro model for the investigation of the regulatory mechanisms of cartilage formation and endochondral ossification.
机译:1.软骨形成是生物学中最复杂的过程之一。本研究的目的是生产简化的体外系统以解决其复杂性。 2.用包含10 ng / mL转化生长因子(TGF)-beta3的软骨形成诱导培养基将人间充质干细胞(hMSC)维持在藻酸盐珠中。 3.在培养的第0、2、4、8、12、16和19天,我们使用光学显微镜和透射电子显微镜检查了细胞。我们还使用免疫低温显微术评估了细胞。 4.本研究表明,hMSC暴露于藻酸盐珠粒中的软骨形成诱导培养基后,会产生许多含有异常胶原纤维的细胞外基质。此时,通过茜素红染色检测到钙化,并且在细胞质和细胞外空间均出现由羟基磷灰石组成的电子致密颗粒。 5.另外,免疫冷冻超显微术还显示II型胶原蛋白,X型胶原蛋白和蛋白聚糖显着,并且在第2天可检测到骨钙蛋白。在培养的8-16天中,X型胶原蛋白保持其强表达,而骨钙蛋白的表达显着增加。 。相反,II型胶原蛋白和蛋白聚糖的表达随时间降低。 6.这些发现表明,hMSC迅速分化成表达II型胶原和蛋白聚糖的软骨细胞。 7.然后,II型胶原蛋白和蛋白聚糖的表达下降,X型胶原蛋白的活性与之前相同(4-8天)。结果,细胞发展为下一种细胞类型,即所谓的肥大性软骨细胞。最后,骨钙素活性以及细胞体和细胞外基质的钙化都变得明显,表明软骨内骨化。因此,我们得出的结论是,hMSC迅速分化为软骨细胞,随后发育为肥大性软骨细胞。软骨内骨化是这种文化的最终形式。 8.本研究的结果表明,我们的三维培养是一种方便的体外模型,可用于研究软骨形成和软骨内骨化的调节机制。

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