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Serum Free Cultured Bone Marrow Mesenchymal Stem Cells as a Platform to Characterize the Effects of Specific Molecules

机译:无血清培养的骨髓间充质干细胞作为表征特定分子作用的平台

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摘要

Human mesenchymal stem cells (hMSC) are easily isolated from the bone marrow by adherence to plastic surfaces. These cells show self-renewal capacity and multipotency. A unique feature of hMSC is their capacity to survive without serum. Under this condition hMSC neither proliferate nor differentiate but maintain their biological properties unaffected. Therefore, this should be a perfect platform to study the biological effects of defined molecules on these human stem cells. We show that hMSC treated for five days with retinoic acid (RA) in the absence of serum undergo several transcriptional changes causing an inhibition of ERK related pathways. We found that RA induces the loss of hMSC properties such as differentiation potential to either osteoblasts or adipocytes. We also found that RA inhibits cell cycle progression in the presence of proliferating signals such as epidermal growth factor (EGF) combined with basic fibroblast growth factor (bFGF). In the same manner, RA showed to cause a reduction in cell adhesion and cell migration. In contrast to these results, the addition of EGF+bFGF to serum free cultures was enough to upregulate ERK activity and induce hMSC proliferation and cell migration. Furthermore, the addition of these factors to differentiation specific media instead of serum was enough to induce either osteogenesis or adipogenesis. Altogether, our results show that hMSC's ability to survive without serum enables the identification of signaling factors and pathways that are involved in their stem cell biological characteristics without possible serum interferences.
机译:人间充质干细胞(hMSC)通过粘附在塑料表面上很容易从骨髓中分离出来。这些细胞显示出自我更新的能力和专长。 hMSC的独特功能是无血清生存能力。在这种情况下,hMSC既不增殖也不分化,但保持其生物学特性不受影响。因此,这应该是研究定义的分子对这些人类干细胞的生物学效应的理想平台。我们显示,在没有血清的情况下,用视黄酸(RA)治疗了五天的hMSC经历了几次转录变化,导致对ERK相关途径的抑制。我们发现RA诱导了hMSC特性的丧失,例如向成骨细胞或脂肪细胞分化的潜能。我们还发现,在增殖信号(例如表皮生长因子(EGF)与碱性成纤维细胞生长因子(bFGF)结合)的存在下,RA抑制细胞周期进程。同样,RA显示出导致细胞粘附和细胞迁移减少的原因。与这些结果相反,向无血清培养物中添加EGF + bFGF足以上调ERK活性并诱导hMSC增殖和细胞迁移。此外,将这些因素添加到分化特异性培养基而不是血清中足以诱导成骨或脂肪形成。总之,我们的结果表明,hMSC在没有血清的情况下生存的能力使得能够鉴定涉及其干细胞生物学特性的信号转导因子和途径,而不会产生血清干扰。

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