Delivery Systems in Neuronal Direct Cell Reprogramming.

IF 1.2 4区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Giulia Redi, Filomena Del Piano, Sara Cappellini, Martina Paladino, Anne den Breejen, Marcel H A M Fens, Massimiliano Caiazzo
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引用次数: 0

Abstract

Neuronal direct cell reprogramming approach allows direct conversion of somatic cells into neurons via forced expression of neuronal cell-lineage transcription factors (TFs). These so-called induced neuronal cells have significant potential as research tools and for therapeutic applications, such as in cell replacement therapy. However, the optimization of TF delivery strategies is crucial to reach clinical practice. In this review, we outlined the currently explored delivery technologies in neuronal direct cell reprogramming and their limitations and advantages. The first employed delivery strategies were mainly integrating viral systems, such as lentiviruses that exert consistently high transgene expression in most cell types. On the other hand, viral systems cause major safety concerns, including the risk for insertional mutagenesis and inflammation. More recently, several safer nonviral delivery systems have been investigated as well; however, these systems generally exert inferior reprogramming efficiency compared with viral systems. Emerging delivery technologies could provide new opportunities in the achievement of safe and effective delivery for neuronal direct cell reprogramming.

神经元直接细胞重编程中的传递系统。
神经元直接细胞重编程方法允许通过强迫表达神经元细胞系转录因子(tf)将体细胞直接转化为神经元。这些所谓的诱导神经元细胞在研究工具和治疗应用方面具有巨大的潜力,例如在细胞替代疗法中。然而,优化TF给药策略是达到临床实践的关键。在这篇综述中,我们概述了目前探索的神经元直接细胞重编程的传递技术及其局限性和优势。最初采用的递送策略主要是整合病毒系统,例如在大多数细胞类型中持续高转基因表达的慢病毒。另一方面,病毒系统引起主要的安全问题,包括插入突变和炎症的风险。最近,人们还研究了几种更安全的非病毒输送系统;然而,与病毒系统相比,这些系统通常表现出较差的重编程效率。新兴的递送技术为实现神经元直接细胞重编程的安全有效递送提供了新的机会。
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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来源期刊
Cellular reprogramming
Cellular reprogramming CELL & TISSUE ENGINEERING-BIOTECHNOLOGY & APPLIED MICROBIOLOGY
CiteScore
2.50
自引率
6.20%
发文量
37
审稿时长
3 months
期刊介绍: Cellular Reprogramming is the premier journal dedicated to providing new insights on the etiology, development, and potential treatment of various diseases through reprogramming cellular mechanisms. The Journal delivers information on cutting-edge techniques and the latest high-quality research and discoveries that are transforming biomedical research. Cellular Reprogramming coverage includes: Somatic cell nuclear transfer and reprogramming in early embryos Embryonic stem cells Nuclear transfer stem cells (stem cells derived from nuclear transfer embryos) Generation of induced pluripotent stem (iPS) cells and/or potential for cell-based therapies Epigenetics Adult stem cells and pluripotency.
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