Paulo Victor Visintin, Bruna Lancia Zampieri, Karina Griesi-Oliveira
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引用次数: 0
Abstract
Introduction: Transdifferentiation is the conversion of a specific somatic cell into another cell type, bypassing a transient pluripotent state. This implies a faster method to generate cells of interest with the additional benefit of reduced tumorigenic risk for clinical use.
Objective: We describe protocols that use small molecules as direct conversion inducers, without the need for exogenous factors, to evaluate the potential of cell transdifferentiation for pharmacological and clinical applications.
Methods: In this systematic review, using PRISMA guidelines, we conducted a personalized search strategy in four databases (PubMed, Scopus, Embase, and Web Of Science), looking for experimental works that used exclusively small molecules for transdifferentiation of non-neural cell types into neural lineage cells.
Results: We explored the main biological mechanisms involved in direct cell conversion induced by different small molecules used in 33 experimental in vitro and in vitro transdifferentiation protocols. We also summarize the main characteristics of these protocols, such as the chemical cocktails used, time for transdifferentiation, and conversion efficiency.
Conclusion: Small molecules-based protocols for neuronal transdifferentiation are reasonably safe, economical, accessible, and are a promising alternative for future use in regenerative medicine and pharmacology.
转分化是一个特定的体细胞转化为另一种细胞类型,绕过一个短暂的多能状态。这意味着一种更快的方法来产生感兴趣的细胞,并具有降低致瘤风险的额外好处,可用于临床。目的:我们描述了使用小分子作为直接转化诱导剂的方案,而不需要外源因素,以评估细胞转分化的药理学和临床应用潜力。方法:在这篇系统综述中,我们使用PRISMA指南,在四个数据库(PubMed, Scopus, Embase和Web Of Science)中进行了个性化搜索策略,寻找专门使用小分子将非神经细胞类型转分化为神经谱系细胞的实验作品。结果:我们探索了33种体外和体外转分化实验方案中不同小分子诱导直接细胞转化的主要生物学机制。我们还总结了这些方案的主要特点,如使用的化学鸡尾酒,转分化时间和转化效率。结论:基于小分子的神经转分化方案是相当安全、经济、可获得的,是未来再生医学和药理学的一个有希望的替代方案。