A mini-review to delineate the different roles of stem cells and Wnt signalling pathways in governing transdifferentiation towards neuronal lineage.

Alakesh Das, Aainaaz Iffath, Keerthi Nethaji, A. Dey, Praveen Rawlo, S. Pathak, A. Banerjee
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Abstract

Mesenchymal stem cells are found to have the potential to differentiate into many lineages, thus regulating diverse signalling cascades. This unique property of stem cells, called trans differentiation/linear reprogramming, aided in regenerative medicine and tissue repair. The mechanism of such regeneration is still unclear and requires further analysis. Due to the use of external or oncogenic factors, one of the approaches for mending cardiac, renal, and neurological disorders after an injury by induced pluripotent stem cells in the form of reprogramming does not show much benefit in the clinical setting. Consequently, cellular reprogramming may enable the application of clinical research to cell therapy, disease modelling, drug screening, and the fabrication of artificial organs. Studies related to this distinctive phenomenon of stem cells, where the cells could reprogramme themselves into completely different cell lineages, showed a promising future in therapeutic applications.  However, unrelenting development in cellular reprogramming has prepared the ways for novel strategies in which signalling pathway manipulation may decide cellular destiny. This cellular reprogramming has got bright prospects in the field of regenerative medicine. Therefore, understanding the relationship between stochasticity and defining cell fate can help decipher molecular regulatory mechanisms of cellular reprogramming.
概述干细胞和Wnt信号通路在调控向神经元谱系转分化中的不同作用。
间充质干细胞被发现有可能分化成许多谱系,从而调节不同的信号级联反应。干细胞的这种独特特性被称为反式分化/线性重编程,有助于再生医学和组织修复。这种再生的机制尚不清楚,需要进一步分析。由于使用外部或致癌因素,一种通过诱导多能干细胞以重编程的形式修复损伤后的心脏、肾脏和神经系统疾病的方法在临床环境中没有显示出太多的益处。因此,细胞重编程可以使临床研究应用于细胞治疗、疾病建模、药物筛选和人造器官的制造。干细胞的这种独特现象,细胞可以重新编程成完全不同的细胞系,与此相关的研究表明,在治疗应用方面有很好的前景。然而,细胞重编程的不断发展为信号通路操纵可能决定细胞命运的新策略铺平了道路。这种细胞重编程技术在再生医学领域有着广阔的应用前景。因此,理解随机性和定义细胞命运之间的关系有助于破译细胞重编程的分子调控机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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