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Differences in the intrinsic chondrogenic potential of equine umbilical cord matrix and cord blood mesenchymal stromal/stem cells for cartilage regeneration

机译:马脐带基质和脐血间充质基质/干细胞在软骨再生中内在软骨生成潜能的差异

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摘要

Umbilical cord blood mesenchymal stromal/stem cells (UCB-MSCs) and umbilical cord matrix MSCs (UCM-MSCs) have chondrogenic potential and are alternative sources to standard surgically derived bone marrow or adipose tissue collection for cartilage engineering. However, the majority of comparative studies explore neonatal MSCs potential only on ISCT benchmark assays accounting for some bias in the reproducibility between in vitro and in clinical studies. Therefore, we characterized equine UCB-MSCs and UCM-MSCs and investigated with particular attention their chondrogenesis potential in 3D culture with BMP-2 + TGF-ß1 in normoxia or hypoxia. We carried out an exhaustive characterization of the extracellular matrix generated by both these two types of MSCs after the induction of chondrogenesis through evaluation of hyaline cartilage, hypertrophic and osteogenic markers (mRNA, protein and histology levels). Some differences in hypoxia sensitivity and chondrogenesis were observed. UCB-MSCs differentiated into chondrocytes express an abundant, dense and a hyaline-like cartilage matrix. By contrast, despite their expression of cartilage markers, UCM-MSCs failed to express a relevant cartilage matrix after chondrogenic induction. Both MSCs types also displayed intrinsic differences at their undifferentiated basal status, UCB-MSCs expressing higher levels of chondrogenic markers whereas UCM-MSCs synthesizing higher amounts of osteogenic markers. Our results suggest that UCB-MSCs should be preferred for ex-vivo horse cartilage engineering. How those results should be translated to in vivo direct cartilage regeneration remains to be determined through dedicated study.
机译:脐带血间充质基质/干细胞(UCB-MSC)和脐带基质MSC(UCM-MSC)具有软骨形成的潜力,并且是用于软骨工程的标准手术来源骨髓或脂肪组织收集的替代来源。但是,大多数比较研究仅在ISCT基准分析中探讨了新生儿MSC的潜力,这说明了体外和临床研究之间的可重复性存在一定偏差。因此,我们对马UCB-MSC和UCM-MSC进行了表征,并特别注意在常氧或低氧条件下用BMP-2 +TGF-ß1进行3D培养的软骨形成潜力。我们通过评价透明软骨,肥大性和成骨性标志物(mRNA,蛋白质和组织学水平),在诱导软骨形成后,对这两种类型的MSC生成的细胞外基质进行了详尽的表征。观察到缺氧敏感性和软骨形成方面的一些差异。分化为软骨细胞的UCB-MSC表达丰富,密集和透明的软骨样基质。相比之下,UCM-MSC尽管表达了软骨标志物,但在软骨诱导后未能表达相关的软骨基质。两种类型的MSC在未分化的基础状态上也都表现出内在差异,UCB-MSC表达更高水平的成软骨标记,而UCM-MSC合成了大量成骨标记。我们的结果表明,UCB-MSCs应优先用于体外软骨工程。如何将这些结果转化为体内直接软骨再生仍需通过专门研究确定。

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