CNRS, IPBS (Institut de Pharmacologie et de Biologie Structurale), 205 route de Narbonne, F-31077 Toulouse, France.
J Control Release. 2011 Jan 20;149(2):117-25. doi: 10.1016/j.jconrel.2010.09.022. Epub 2010 Oct 1.
Gene transfer into muscle cells is a key issue in biomedical research. Indeed, it is important for the development of new therapy for many genetic disorders affecting this tissue and for the use of muscle tissue as a secretion platform of therapeutic proteins. Electrotransfer is a promising method to achieve gene expression in muscles. However, this method can lead to some tissue damage especially on pathologic muscles. Therefore there is a need for the development of new and less deleterious methods. Triblock copolymers as pluronic L64 are starting to be used to improve gene transfer mediated by several agents into muscle tissue. Their mechanism of action is still under investigation. The combination of electrotransfer and triblock copolymers, in allowing softening electric field conditions leading to efficient DNA transfection, could potentially represent a milder and more secure transfection method. In the present study, we addressed the possible synergy that could be obtained by combining the copolymer triblock L64 and electroporation. We have found that a pre-treatment of cells with L64 could improve the transfection efficiency. This pre-treatment was shown to increase cell viability and this is partly responsible for the improvement of transfection efficiency. We have then labelled the plasmid DNA and the pluronic L64 in order to gain some insights into the mechanism of transfection of the combined physical and chemical methods. These experiences allowed us to exclude an action of L64 either on membrane permeabilization or on DNA/membrane interaction. Using plasmids containing or not binding sequences for NF-κB and an inhibitor of NF-κB pathway activation we have shown that this beneficial effect was rather related to the NF-κB signalling pathway, as it is described for other pluronics. Finally we address here some mechanistic issues on electrically mediated transfection, L64 mediated membrane permeabilization and the combination of both for gene transfer.
将基因转入肌肉细胞是生物医学研究中的一个关键问题。事实上,对于开发许多影响这种组织的遗传疾病的新疗法,以及利用肌肉组织作为治疗蛋白的分泌平台,这一点非常重要。电转移是实现肌肉中基因表达的一种很有前途的方法。然而,这种方法可能会导致一些组织损伤,特别是在病理肌肉上。因此,需要开发新的、危害较小的方法。嵌段共聚物如 Pluronic L64 开始被用于改善几种药物介导的基因转移到肌肉组织中的效果。其作用机制仍在研究中。电转移和嵌段共聚物的结合,通过允许软化电场条件来实现有效的 DNA 转染,可能代表一种更温和、更安全的转染方法。在本研究中,我们探讨了通过结合嵌段共聚物 L64 和电穿孔来获得协同作用的可能性。我们发现,L64 预处理可以提高转染效率。这种预处理被证明可以提高细胞活力,这也是提高转染效率的部分原因。然后,我们对质粒 DNA 和 Pluronic L64 进行了标记,以便深入了解物理和化学联合方法的转染机制。这些经验使我们排除了 L64 对膜通透性或 DNA/膜相互作用的作用。使用含有或不含有 NF-κB 结合序列的质粒和 NF-κB 途径激活抑制剂,我们表明这种有益的效果与 NF-κB 信号通路有关,正如其他 Pluronics 所描述的那样。最后,我们在这里讨论了一些与电介导转染、L64 介导的膜通透性以及两者结合用于基因转移的机制问题。