咖啡因诱导的基因开关控制实验性糖尿病。
Caffeine-inducible gene switches controlling experimental diabetes.
机构信息
Department of Biosystems Science and Engineering, ETH Zurich, Mattenstrasse 26, 4058, Basel, Switzerland.
IUT, Département Génie Biologique, Institut Universitaire de Technologie, F-69622, Villeurbanne Cedex, France.
出版信息
Nat Commun. 2018 Jun 19;9(1):2318. doi: 10.1038/s41467-018-04744-1.
Programming cellular behavior using trigger-inducible gene switches is integral to synthetic biology. Although significant progress has been achieved in trigger-induced transgene expression, side-effect-free remote control of transgenes continues to challenge cell-based therapies. Here, utilizing a caffeine-binding single-domain antibody we establish a caffeine-inducible protein dimerization system, enabling synthetic transcription factors and cell-surface receptors that enable transgene expression in response to physiologically relevant concentrations of caffeine generated by routine intake of beverages such as tea and coffee. Coffee containing different caffeine concentrations dose-dependently and reversibly controlled transgene expression by designer cells with this caffeine-stimulated advanced regulators (C-STAR) system. Type-2 diabetic mice implanted with microencapsulated, C-STAR-equipped cells for caffeine-sensitive expression of glucagon-like peptide 1 showed substantially improved glucose homeostasis after coffee consumption compared to untreated mice. Biopharmaceutical production control by caffeine, which is non-toxic, inexpensive and only present in specific beverages, is expected to improve patient compliance by integrating therapy with lifestyle.
利用触发诱导基因开关来编程细胞行为是合成生物学的基础。尽管在触发诱导转基因表达方面已经取得了重大进展,但无副作用的转基因远程控制仍然是细胞疗法的挑战。在这里,我们利用咖啡因结合的单域抗体建立了一种咖啡因诱导的蛋白质二聚化系统,该系统可用于合成转录因子和细胞表面受体,使转基因能够响应于茶和咖啡等常规饮料中产生的生理相关浓度的咖啡因进行表达。含有不同咖啡因浓度的咖啡通过具有这种咖啡因刺激的高级调节剂 (C-STAR) 系统的设计细胞以剂量依赖和可逆的方式控制转基因表达。植入用微囊包封的、配备有 C-STAR 的细胞的 2 型糖尿病小鼠在饮用咖啡后与未处理的小鼠相比,表现出明显改善的葡萄糖稳态。通过使用非毒性、廉价且仅存在于特定饮料中的咖啡因来控制生物制药生产,预计通过将治疗与生活方式相结合来提高患者的依从性。