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首页> 外文期刊>Scientific reports. >Chondrogenic commitment of human umbilical cord blood-derived mesenchymal stem cells in collagen matrices for cartilage engineering
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Chondrogenic commitment of human umbilical cord blood-derived mesenchymal stem cells in collagen matrices for cartilage engineering

机译:软骨基质中人脐带血间充质干细胞在胶原蛋白基质中的软骨生成承诺

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摘要

Umbilical cord blood (UCB) is a promising alternative source of mesenchymal stem cells (MSCs), because UCB-MSCs are abundant and harvesting them is a painless non-invasive procedure. Potential clinical applications of UCB-MSCs have been identified, but their ability for chondrogenic differentiation has not yet been fully evaluated. The aim of our work was to characterize and determine the chondrogenic differentiation potential of human UCB-MSCs (hUCB-MSCs) for cartilage tissue engineering using an approach combining 3D culture in type I/III collagen sponges and chondrogenic factors. Our results showed that UCB-MSCs have a high proliferative capacity. These cells differentiated easily into an osteoblast lineage but not into an adipocyte lineage. Furthermore, BMP-2 and TGF-β1 potentiated chondrogenic differentiation, as revealed by a strong increase in mature chondrocyte-specific mRNA (COL2A1, COL2B, ACAN) and protein (type II collagen) markers. Although growth factors increased the transcription of hypertrophic chondrocyte markers such as COL10A1 and MMP13, the cells present in the neo-tissue maintained their phenotype and did not progress to terminal differentiation and mineralization of the extracellular matrix after subcutaneous implantation in nude mice. Our study demonstrates that our culture model has efficient chondrogenic differentiation, and that hUCB-MSCs can be a reliable source for cartilage tissue engineering.
机译:脐带血(UCB)是间充质干细胞(MSC)的一种有前途的替代来源,因为UCB-MSC丰富且收获无痛,无创。已经确定了UCB-MSC的潜在临床应用,但尚未充分评估其软骨分化的能力。我们工作的目的是使用结合I / III型胶原海绵中的3D培养和软骨形成因子的方法,表征和确定人UCB-MSC(hUCB-MSC)在软骨组织工程中的软骨分化潜能。我们的结果表明,UCB-MSC具有很高的增殖能力。这些细胞容易分化为成骨细胞谱系,而不分化为脂肪细胞谱系。此外,BMP-2和TGF-β1增强了软骨形成的分化,如成熟的软骨细胞特异性mRNA(COL2A1,COL2B,ACAN)和蛋白质(II型胶原)标志物的强烈增加所揭示的。尽管生长因子增加了肥大性软骨细胞标志物(例如COL10A1和MMP13)的转录,但是在裸鼠皮下植入后,新组织中存在的细胞保持了其表型,并没有进展到细胞外基质的终末分化和矿化。我们的研究表明我们的培养模型具有有效的软骨分化能力,并且hUCB-MSCs可以作为软骨组织工程的可靠来源。

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