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Highly branched  poly(β-amino ester) delivery of minicircle DNA for transfection of neurodegenerative disease related cells

机译:微环DNA的高度分支聚(β-氨基酯)传递用于神经退行性疾病相关细胞的转染

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摘要

Current therapies for most neurodegenerative disorders are only symptomatic in nature and do not change the course of the disease. Gene therapy plays an important role in disease modifying therapeutic strategies. Herein, we have designed and optimized a series of highly branched poly(β-amino ester)s (HPAEs) containing biodegradable disulfide units in the HPAE backbone (HPAESS) and guanidine moieties (HPAESG) at the extremities. The optimized polymers are used to deliver minicircle DNA to multipotent adipose derived stem cells (ADSCs) and astrocytes, and high transfection efficiency is achieved (77% in human ADSCs and 52% in primary astrocytes) whilst preserving over 90% cell viability. Furthermore, the top-performing candidate mediates high levels of nerve growth factor (NGF) secretion from astrocytes, causing neurite outgrowth from a model neuron cell line. This synergistic gene delivery system provides a viable method for highly efficient non-viral transfection of ADSCs and astrocytes.
机译:目前大多数神经退行性疾病的治疗方法仅是对症治疗,不会改变病程。基因治疗在改变疾病的治疗策略中起着重要作用。本文中,我们设计并优化了一系列高度分支的聚(β-氨基酯)(HPAE),其中HPAE主链(HPAESS)和胍基(HPAESG)包含可生物降解的二硫键单元。经过优化的聚合物用于将小环DNA递送至多能脂肪衍生干细胞(ADSC)和星形胶质细胞,并实现了高转染效率(在人类ADSC中为77%,在原代星形胶质细胞中为52%),同时保留了90%以上的细胞活力。此外,表现最佳的候选药物介导星形胶质细胞分泌高水平的神经生长因子(NGF),从而导致神经元从模型神经元细胞系中长出。这种协同的基因传递系统为ADSC和星形胶质细胞的高效非病毒转染提供了可行的方法。

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