...
首页> 外文期刊>Stem cells international >Genetic Markers Can Predict Chondrogenic Differentiation Potential in Bone Marrow-Derived Mesenchymal Stromal Cells
【24h】

Genetic Markers Can Predict Chondrogenic Differentiation Potential in Bone Marrow-Derived Mesenchymal Stromal Cells

机译:遗传标记可以预测骨髓源间充质基质细胞的软骨分化潜能。

获取原文
           

摘要

The precise predictions of the differentiation direction and potential of mesenchymal stromal cells (MSCs) are an important key to the success of regenerative medicine. The expression levels of fate-determining genes may provide tools for predicting differentiation potential. The expression levels of 95 candidate marker genes and glycosaminoglycan (GAG) contents after chondrogenic induction in 10 undifferentiated ilium and 5 jaw MSC cultures were determined, and their correlations were analyzed. The expression levels of eight genes before the induction of chondrogenic MSC differentiation were significantly correlated with the GAG levels after induction. Based on correlation patterns, the eight genes were classified into two groups group 1 genes (AURKB, E2F1, CDKN2D, LIF, and ACLY), related to cell cycle regulation, and group 2 genes (CD74, EFEMP1, and TGM2), involved in chondrogenesis. The expression levels of the group 2 genes were significantly correlated with the ages of the cell donors. The expression levels of CDKN2D, CD74, and TGM2 were >10-fold higher in highly potent MSCs (ilium MSCs) than in MSCs with limited potential (jaw MSCs). Three-dimensional (3D) scatter plot analyses of the expression levels of these genes showed reduced variability between donors and confirmed predictive potential. These data suggest that group 2 genes are involved in age-dependent decreases in the chondrogenic differentiation potential of MSCs, and combined 3D analyses of the expression profiles of three genes, including two group 2 genes, were predictive of MSC differentiation potential.
机译:间充质基质细胞(MSCs)分化方向和潜能的精确预测是再生医学成功的重要关键。命运决定基因的表达水平可能提供预测分化潜能的工具。测定了95种候选标记基因的表达水平和成软骨诱导后在10种未分化的lium骨和5种颌骨MSC培养物中的糖胺聚糖含量,并分析了它们之间的相关性。诱导软骨形成MSC分化之前的八个基因的表达水平与诱导后GAG水平显着相关。根据相关性模式,将这八个基因分为与细胞周期调控有关的第1组基因(AURKB,E2F1,CDKN2D,LIF和ACLY)和第2组基因(CD74,EFEMP1和TGM2)。软骨形成。第2组基因的表达水平与细胞供体的年龄显着相关。在高效MSC(ilium MSC)中,CDKN2D,CD74和TGM2的表达水平比潜力有限的MSC(下颚MSC)高10倍以上。这些基因的表达水平的三维(3D)散点图分析显示供体之间的变异性降低,并证实了预测潜力。这些数据表明,第2组基因参与了MSCs软骨分化潜能的年龄依赖性降低,并且对3个基因(包括2个第2组基因)的表达谱进行了3D分析,共同预测了MSC的分化潜能。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号