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首页> 外文期刊>BMC Musculoskeletal Disorders >Different culture media affect growth characteristics, surface marker distribution and chondrogenic differentiation of human bone marrow-derived mesenchymal stromal cells
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Different culture media affect growth characteristics, surface marker distribution and chondrogenic differentiation of human bone marrow-derived mesenchymal stromal cells

机译:不同的培养基会影响人骨髓间充质基质细胞的生长特性,表面标志物分布和软骨分化

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Background Bone marrow-derived mesenchymal stromal cells (BM-MSCs) play an important role in modern tissue engineering, while distinct variations of culture media compositions and supplements have been reported. Because MSCs are heterogeneous regarding their regenerative potential and their surface markers, these parameters were compared in four widely used culture media compositions. Methods MSCs were isolated from bone marrow and expanded in four established cell culture media. MSC yield/1000 MNCs, passage time and growth index were observed. In P4, typical MSC surface markers were analysed by fluorescence cytometry. Additionally, chondrogenic, adipogenic and osteogenic differentiation potential were evaluated. Results Growth index and P0 cell yield varied importantly between the media. The different expansion media had a significant influence on the expression of CD10, CD90, CD105, CD140b CD146 and STRO-1. While no significant differences were observed regarding osteogenic and adipogenic differentiation, chondrogenic differentiation was superior in medium A as reflected by GAG/DNA content. Conclusions The choice of expansion medium can have a significant influence on growth, differentiation potential and surface marker expression of mesenchymal stromal cells, which is of fundamental importance for tissue engineering procedures.
机译:背景技术骨髓来源的间充质基质细胞(BM-MSC)在现代组织工程中起着重要的作用,而培养基成分和补品的不同变化也已有报道。由于MSC的再生潜力和表面标记是异质的,因此在四种广泛使用的培养基成分中比较了这些参数。方法从骨髓中分离MSC,并在四种已建立的细胞培养基中扩增。观察到MSC产量/ 1000个MNC,通过时间和生长指数。在P4中,通过荧光细胞计数法分析了典型的MSC表面标记。另外,评估了软骨形成,脂肪形成和成骨分化的潜力。结果在不同培养基之间,生长指数和P0细胞产量差异很大。不同的膨胀培养基对CD10,CD90,CD105,CD140b,CD146和STRO-1的表达有重要影响。尽管在成骨和脂肪形成分化方面未观察到显着差异,但GAG / DNA含量反映出软骨形成在A培养基中的分化更好。结论扩增培养基的选择对间充质基质细胞的生长,分化潜能和表面标志物的表达有重要影响,这对组织工程程序至关重要。

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