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首页> 外文期刊>Biological research: BR >The gene suicide system NTR/CB1954 causes ablation of differentiated 3T3L1 adipocytes by apoptosis
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The gene suicide system NTR/CB1954 causes ablation of differentiated 3T3L1 adipocytes by apoptosis

机译:自杀基因系统NTR / CB1954通过凋亡引起分化的3T3L1脂肪细胞消融

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摘要

The feasibility of ablating differentiated adipocytes and the mechanism of cell ablation with a suitable prodrug activating system is described. The system is based on the use of E. coli nitroreductase (NTR) enzyme that activates certain nitro compounds, such as the antitumor drug CB1954, into cytotoxic DNA interstrand cross-linking agents. Differentiated preadipocyte cells (3T3L1) transfected with an aP2 driven nitroreductase construct were efficiently killed after incubation with medium containing the prodrug CB1954, while untransfected cells were not affected. It was demonstrated that the mechanism of cell ablation is apoptosis and that the system has a bystander effect mediated by a toxic metabolite of the prodrug. The described system should provide a good alternative approach for gene therapy studies and a new inducible approach to manipulating the number of cells in tissues of transgenic animals and the ability to study the recovery of the tissue from cell damage or loss
机译:描述了用合适的前药激活系统消融分化的脂肪细胞的可行性和细胞消融的机制。该系统基于使用大肠杆菌硝基还原酶(NTR)酶,该酶将某些硝基化合物(例如抗肿瘤药CB1954)活化为细胞毒性DNA链间交联剂。与含有前药CB1954的培养基孵育后,用aP2驱动的硝基还原酶构建体转染的分化前脂肪细胞(3T3L1)被有效杀死,而未转染的细胞不受影响。已经证明,细胞消融的机制是凋亡,并且该系统具有由前药的毒性代谢产物介导的旁观者效应。所描述的系统应该为基因疗法研究提供良好的替代方法,并为操纵转基因动物组织中的细胞数量以及研究从细胞损伤或丢失中恢复组织的能力提供新的诱导方法。

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