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Cyclin-dependent kinase 4 signaling acts as a molecular switch between syngenic differentiation and neural transdifferentiation in human mesenchymal stem cells

机译:细胞周期蛋白依赖性激酶4信号作为人类间充质干细胞同基因分化和神经转分化之间的分子开关

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摘要

Multipotent mesenchymal stem/stromal cells (MSCs) are capable of differentiating into a variety of cell types from different germ layers. However, the molecular and biochemical mechanisms underlying the transdifferentiation of MSCs into specific cell types still need to be elucidated. In this study, we unexpectedly found that treatment of human adipose- and bone marrow-derived MSCs with cyclin-dependent kinase (CDK) inhibitor, in particular CDK4 inhibitor, selectively led to transdifferentiation into neural cells with a high frequency. Specifically, targeted inhibition of CDK4 expression using recombinant adenovial shRNA induced the neural transdifferentiation of human MSCs. However, the inhibition of CDK4 activity attenuated the syngenic differentiation of human adipose-derived MSCs. Importantly, the forced regulation of CDK4 activity showed reciprocal reversibility between neural differentiation and dedifferentiation of human MSCs. Together, these results provide novel molecular evidence underlying the neural transdifferentiation of human MSCs; in addition, CDK4 signaling appears to act as a molecular switch from syngenic differentiation to neural transdifferentiation of human MSCs.
机译:多能间充质干/基质细胞(MSC)能够从不同的细菌层分化为多种细胞类型。但是,仍然需要阐明将MSCs转分化为特定细胞类型的分子和生化机制。在这项研究中,我们出乎意料地发现,用细胞周期蛋白依赖性激酶(CDK)抑制剂,特别是CDK4抑制剂治疗人脂肪和骨髓来源的MSCs,有选择地导致转分化为高频神经细胞。具体而言,使用重组腺病毒shRNA靶向抑制CDK4表达可诱导人MSC的神经转分化。但是,对CDK4活性的抑制减弱了人脂肪来源的MSC的同基因分化。重要的是,CDK4活性的强制调节显示了人类MSC的神经分化和去分化之间的相互可逆性。在一起,这些结果提供了人类MSCs神经转分化基础的新颖分子证据。此外,CDK4信号似乎起着人类MSC从同基因分化到神经转分化的分子转换。

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