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利用改良的前药转化硝基还原酶进行选择性细胞消融。

Selective Cell Ablation Using an Improved Prodrug-Converting Nitroreductase.

机构信息

Department of Ophthalmology, Wilmer Eye Institute, Johns Hopkins University, Baltimore, MD, USA.

出版信息

Methods Mol Biol. 2024;2707:223-234. doi: 10.1007/978-1-0716-3401-1_15.

Abstract

Selective cell ablation is an invaluable tool to investigate the function of cell types, the regeneration of cells, and the modeling of diseases associated with cell loss. The nitroreductase (NTR)-mediated cell ablation system is a simple method enabling the elimination of targeted cells through the expression of a nitroreductase enzyme and the application of a prodrug (such as metronidazole). The prodrug is reduced to a cytotoxic product by nitroreductase, thereby leading to DNA damage-induced cell death. In species with elevated regenerative capacity such as zebrafish, removing the prodrug allows endogenous tissue to replace the lost cells. Herein, we describe a method for the use of a markedly improved nitroreductase enzyme for spatially and temporally controlled targeted cell ablation in the zebrafish. Recently, we identified an NTR variant (NTR 2.0) that achieves effective targeted cell ablation at concentrations of metronidazole well below those causing toxic side effects. NTR 2.0 thereby enables the ablation of "resistant" cell types and novel cell ablation paradigms. These advances simplify investigations of cell function, enable interrogations of the effects of chronic inflammation on regenerative processes and facilitate modeling of degenerative diseases associated with chronic cell loss. Techniques for transgenic nitroreductase expression and prodrug application are discussed.

摘要

选择性细胞消融是一种非常有价值的工具,可用于研究细胞类型的功能、细胞的再生以及与细胞丢失相关的疾病建模。硝基还原酶(NTR)介导的细胞消融系统是一种简单的方法,通过表达硝基还原酶酶和应用前药(如甲硝唑)来消除靶向细胞。前药被硝基还原酶还原为细胞毒性产物,从而导致 DNA 损伤诱导的细胞死亡。在具有较高再生能力的物种(如斑马鱼)中,去除前药可以使内源性组织取代丢失的细胞。在此,我们描述了一种在斑马鱼中使用显著改进的硝基还原酶酶进行空间和时间控制的靶向细胞消融的方法。最近,我们鉴定了一种 NTR 变体(NTR 2.0),它可以在低于引起毒副作用的浓度下有效地实现靶向细胞消融。NTR 2.0 从而能够消融“耐药”细胞类型和新型细胞消融范例。这些进展简化了细胞功能的研究,能够研究慢性炎症对再生过程的影响,并有助于模拟与慢性细胞丢失相关的退行性疾病。讨论了用于转基因硝基还原酶表达和前药应用的技术。

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