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Evaluation of in vitro chondrocytic differentiation: A stem cell research initiative at the King Abdulaziz University Kingdom of Saudi Arabia

机译:体外软骨细胞分化的评估:沙特阿拉伯王国阿卜杜勒阿齐兹国王大学的干细胞研究计划

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摘要

Mesenchymal stem cells (MSCs) from various sources have been used in cartilage differentiation with variable success. Therefore, it is of interest to evaluate the in vitro differentiation potential of the hWJSCs derived from the human umbilical cords into chondrocytes at the stem cell research facility at the King Abdulaziz University. hWJSCs are an attractive choice for tissue engineering and regenerative medical applications including cartilage regeneration. We evaluated the hWJSCs using classical histological and cartilage related gene expression studies. Some of the known parameters were re-examined for consistency at the current laboratory conditions. Early passages (P1-P4) showed short fibroblastic morphology and high expression of MSC related surface markers namely CD29 (99.9%), CD44 (97.8%), CD73 (99.6%), CD90 (95.1%) and CD105 (98.9%). MTT assay showed time dependent increase in hWJSCs proliferation by 61.06% and 206.31% at 48h and 72h respectively. Toluidine blue histology showed that hWJSCs were successfully differentiated into chondrocytes in chondrocytic differentiation medium for 21 days. Differentiated hWJSCs also showed significantly increased expression of collagen type II, aggrecan and SOX9 compared to the undifferentiated control. It should be noted that the determination of the average cell yield, the population doubling time and histological staining wtih alcian blue and/or safronin O is required in future studies for improved evaluation of differentiation. Painless derivation, abundance of stem cells that are hypo-immunogenic and safety issues makes this method advantages to MSCs derived from other sources.
机译:来自各种来源的间充质干细胞(MSCs)已成功用于软骨分化。因此,在阿卜杜勒阿齐兹国王大学的干细胞研究机构评估源自人脐带的hWJSCs体外分化为软骨细胞的潜力是令人感兴趣的。 hWJSC是组织工程和包括软骨再生在内的再生医学应用的理想选择。我们使用经典的组织学和软骨相关基因表达研究评估了hWJSC。在当前的实验室条件下,重新检查了一些已知参数的一致性。早期传代(P1-P4)显示出短的成纤维细胞形态和高表达的MSC相关表面标记,即CD29(99.9%),CD44(97.8%),CD73(99.6%),CD90(95.1%)和CD105(98.9%)。 MTT分析显示,在48h和72h,hWJSCs增殖的时间依赖性增加分别为61.06%和206.31%。甲苯胺蓝组织学表明,在软骨细胞分化培养基中,hWJSCs成功分化为软骨细胞21天。与未分化的对照相比,分化的hWJSCs还显示II型胶原蛋白,聚集蛋白聚糖和SOX9的表达显着增加。应当注意的是,在未来的研究中需要确定平均细胞产量,群体倍增时间以及用阿尔辛蓝和/或番红花O进行组织学染色以改善分化评估。无痛衍生,低免疫原性和安全性问题的干细胞丰富使该方法相对于其他来源的MSC具有优势。

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