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Comparative Study on In Vitro Culture of Mouse Bone Marrow Mesenchymal Stem Cells

机译:小鼠骨髓间充质干细胞体外培养的比较研究

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In vitro culture of mesenchymal stem cells (MSCs) from mouse bone marrow (BM) has been hampered because of the low yield of MSCs during isolation and the contamination of hematopoietic cells during expansion. The lack of specific mouse BM-MSC markers increases the difficulty. Several techniques have been reported to improve the purity and in vitro growth of mouse BM-MSCs. However, systematic report on comparison of characteristics in primary BM-MSCs between different culture conditions is rare. Here, we studied the effects of oxygen concentrations and initial medium replacement intervals, along with cell passages, on mouse BM-MSCs isolated with differential adhesion method. BM-MSCs exhibited elevated proliferative and clonogenic abilities in 5% oxygen compared with 10% and 21% oxygen, as well as a better expression of the MSC marker Sca-1. Adipogenic and osteogenetic differentiation of BM-MSCs can be observed in both 21% and 5% oxygen. Adipogenic differentiation appeared stronger under normoxia conditions. BM-MSCs showed increased proliferative capacity and adipogenic/osteogenetic differentiation potential when initial medium replacement interval was 4 days compared with 1 day. As passage number increased, cells were more MSC-like in morphology and in expression of surface markers (positive for CD29, CD44, and Sca-1 and negative for CD11b, CD19, and CD45). These data provide new insight into optimizing the culture method and understanding the biological characteristics of mouse BM-MSCs during in vitro expansion.
机译:由于分离过程中MSC的产量低以及扩增过程中造血细胞的污染,小鼠骨髓(BM)的间充质干细胞(MSC)的体外培养受到阻碍。缺乏特异性小鼠BM-MSC标记物增加了难度。据报道,有几种技术可以改善小鼠BM-MSC的纯度和体外生长。然而,关于不同培养条件之间原代BM-MSCs特征比较的系统报道很少。在这里,我们研究了氧浓度和初始培养基更换间隔以及细胞传代对差异粘附法分离的小鼠BM-MSC的影响。与10%和21%的氧气相比,BM-MSC在5%的氧气中表现出较高的增殖和克隆能力,并且MSC标记Sca-1的表达更好。在21%和5%的氧气中均可观察到BM-MSC的成脂和成骨分化。在常氧条件下,成脂分化似乎更强。当初始培养基更换间隔为4天而不是1天时,BM-MSC的增殖能力和成脂/成骨分化潜能增加。随着传代次数的增加,细胞在形态和表面标志物的表达上更像类MSC(CD29,CD44和Sca-1阳性,而CD11b,CD19和CD45阴性)。这些数据为优化培养方法和了解小鼠BM-MSC在体外扩增过程中的生物学特性提供了新的见识。

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