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An Insight into Reprogramming Barriers to iPSC Generation

机译:对IPSC生成重新编程障碍的洞察

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Derivation of induced Pluripotent Stem Cells (iPSCs) by reprogramming somatic cells to a pluripotent state has revolutionized stem cell research. Ensuing this, various groups have used genetic and non-genetic approaches to generate iPSCs from numerous cell types. However, achieving a pluripotent state in most of the reprogramming studies is marred by serious limitations such as low reprogramming efficiency and slow kinetics. These limitations are mainly due to the presence of potent barriers that exist during reprogramming when a mature cell is coaxed to achieve a pluripotent state. Several studies have revealed that intrinsic factors such as non-optimal stoichiometry of reprogramming factors, specific signaling pathways, cellular senescence, pluripotency-inhibiting transcription factors and microRNAs act as a roadblock. In addition, the epigenetic state of somatic cells and specific epigenetic modifications that occur during reprogramming also remarkably impede the generation of iPSCs. In this review, we present a comprehensive overview of the barriers that inhibit reprogramming and the understanding of which will pave the way to develop safe strategies for efficient reprogramming.
机译:通过重新编程体细胞对多能状态进行诱导多能干细胞(IPSC)的衍生已彻底改变干细胞研究。随之而来,各种组使用遗传和非遗传方法来产生来自许多细胞类型的IPSC。然而,在大多数重新编程研究中实现多能状态是受到严重限制的影响,例如低重编程效率和缓慢动力学。这些限制主要是由于在鞍时重新编程期间存在的有效屏障,以实现多能状态。几项研究表明,诸如非最佳化学计量的重编程因子,特定信号途径,细胞衰老,多能抑制转录因子和微大罗斯作为障碍的内在因素。此外,在重编程期间发生体细胞和特异性表观遗传修饰的表观遗传状态也显着地阻碍了IPSC的产生。在这篇综述中,我们全面概述了抑制重编程的障碍和对其的理解,将为发展安全策略提供高效的重新编程。

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