哺乳动物细胞双调控基因表达:基因治疗的新途径

M. Fussenegger
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引用次数: 12

摘要

多种异源哺乳动物基因调控系统目前可用于人类基因治疗和组织工程。虽然各个基因调控概念在关键特征(调控谱、基础表达水平、人体相容性、免疫原性、药代动力学和诱导剂的生物利用度)上存在显著差异,但它们中的大多数都得到了充分阐述,可以用于临床前研究和临床基因治疗试验。随着前沿基础研究将哺乳动物细胞的细胞周期、分化和凋亡调控网络描述为一个日益复杂的高度互联的球形调控,很明显,许多人类疾病可能源于关键调控基因的最轻微表达失衡。我们认为,成功的基因治疗这些疾病将涉及复杂的多(水平)调控的多基因干预,该干预基于几种人类相容的异源基因调控系统的组合,使治疗干预与细胞调控的最佳整合以及几种治疗性转基因的良好平衡表达。虽然这种多调控的多基因表达场景仍然是一个愿景,但以下已经是培养细胞的科学现实:(1)结合两种人类相容的基因调控系统,使双调控表达技术能够独立调节两种不同的基因活性;(2)多级调控的多基因干预的调控级联;(3)双自动调控的表达配置,用于一步安装多级或相互调节异种基因表达。本文综述了建立双调控表达技术的开创性工作,双调控表达是一种结合多个异源基因调控系统的策略,以实现与基因治疗、组织工程和基础研究相关的难以获得的细胞表型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dual-regulated gene expression in mammalian cells, a novel approach to gene therapy
A variety of heterologous mammalian gene regulation systems are currently available for use in human gene therapy and tissue engineering. While individual gene regulation concepts vary significantly in key characteristics (regulation profiles, basal expression levels, human compatibility, immunogenicity, pharmacokinetics and bioavailability of the inducing agent), most of them are sufficiently elaborated to be considered for preclinical research and clinical gene therapy trials. As forefront basic research describes the cell-cycle, differentiation and apoptosis regulatory networks in mammalian cells as an increasingly complex highly interconnected globular regulon, it becomes apparent that many human diseases may originate from the slightest expression imbalances of key regulatory genes. We believe that successful gene therapy of such diseases will involve complex multi-(level) regulated multigene interventions based on a combination of several human-compatible heterologous gene regulation systems which enable optimal integration of therapeutic interventions into the cellular regulon as well as well-balanced expression of several therapeutic transgenes. Although such multiregulated multigene expression scenarios are still a vision, the following are already a scientific reality with cultured cells: (i) combination of two human compatible gene regulation systems to enable dual-regulated expression technology for independent adjustment of two different gene activities, (ii) regulatory cascades for muli-level regulated multigene interventions, and (iii) dual-autoregulated expression configurations for one-step installation of multi-level or reciprocal regulation of heterologous gene expression. This review summarizes pioneering efforts to establish dual-regulated expression technology, a strategy to combine more than one heterologous gene regulation system, to achieve difficult-to-attain cell phenotypes relevant for gene therapy, tissue engineering and basic research.
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