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Analysis of the Intrinsic Self-Organising Properties of Mesenchymal Stromal Cells in Three-Dimensional Co-Culture Models with Endothelial Cells

机译:三维共培养模型与内皮细胞间充质基质细胞内在自组织特性的分析

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Mesenchymal stem/stromal cells (MSCs) are typically characterised by their ability to differentiate into skeletal (osteogenic, chondrogenic and adipogenic) lineages. MSCs also appear to have additional non-stem cell functions in coordinating tissue morphogenesis and organising vascular networks through interactions with endothelial cells (ECs). However, suitable experimental models to examine these apparently unique MSC properties are lacking. Following previous work, we have developed our 3D in vitro co-culture models to enable us to track cellular self-organisation events in heterotypic cell spheroids combining ECs, MSCs and their differentiated progeny. In these systems, MSCs, but not related fibroblastic cell types, promote the assembly of ECs into interconnected networks through intrinsic mechanisms, dependent on the relative abundance of MSC and EC numbers. Perturbation of endogenous platelet-derived growth factor (PDGF) signalling significantly increased EC network length, width and branching. When MSCs were pre-differentiated towards an osteogenic or chondrogenic lineage and co-cultured as mixed 3D spheroids, they segregated into polarised osseous and chondral regions. In the presence of ECs, the pre-differentiated MSCs redistributed to form a central mixed cell core with an outer osseous layer. Our findings demonstrate the intrinsic self-organising properties of MSCs, which may broaden their use in regenerative medicine and advance current approaches.
机译:间充质干/基质细胞(MSC)通常以分化为骨骼(成骨,成软骨和成脂)谱系的能力为特征。 MSC在通过与内皮细胞(EC)的相互作用来协调组织形态发生和组织血管网络方面似乎还具有其他非干细胞功能。但是,缺乏合适的实验模型来检查这些表面上独特的MSC特性。在先前的工作之后,我们已经开发了3D体外共培养模型,以使我们能够跟踪结合EC,MSC及其分化后代的异型细胞球体中的细胞自组织事件。在这些系统中,MSC(而不是相关的成纤维细胞类型)通过内在机制促进EC组装成相互连接的网络,这取决于MSC和EC数量的相对丰度。内源性血小板衍生生长因子(PDGF)信号的摄动显着增加EC网络的长度,宽度和分支。当MSC向成骨或成软骨谱系预分化并以混合3D球体的形式共培养时,它们分离成极化的骨和软骨区域。在存在EC的情况下,预分化的MSC会重新分布,以形成具有外骨层的中央混合细胞核。我们的发现证明了MSC固有的自组织特性,这可能会拓宽其在再生医学中的应用并发展当前的方法。

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