Department of Pharmaceutical Technology, The German University in Cairo (GUC), Cairo, Egypt.
Department of Biochemistry, The German University in Cairo (GUC), Cairo, Egypt.
Curr Pharm Des. 2023;29(17):1341-1360. doi: 10.2174/1381612829666230601122846.
Reduced cell surface expression or the malfunctioning of ion channels gives rise to a group of disorders known as channelopathies. To treat the underlying cause, the delivery and/or expression of a functional ion channel into the cell membrane of the cell of interest is required. Unfortunately, for most channelopathies, current treatment options are only symptomatic and treatments that rectify the underlying damage are still lacking. Within this context, approaches that rely on gene and protein therapy are required. Gene therapy would allow the expression of a functional protein, provided that the cellular machinery in the diseased cell could correctly fold and traffic the protein to the cell membrane. Whereas protein therapy would allow the direct delivery of a functional protein, provided that the purification process does not affect protein function and a suitable delivery vehicle for targeted delivery is used. In this review, we provide an overview of channelopathies and available symptomatic treatments. The current state of gene therapy approaches mainly using viral vectors is discussed, which is followed by the role of nanomedicine in protein therapy and how nanomedicine could be exploited for the delivery of functional ion channels to diseased cells.
细胞表面表达减少或离子通道功能障碍会导致一组被称为通道病的疾病。为了治疗根本原因,需要将功能性离子通道递送到感兴趣的细胞的细胞膜中。不幸的是,对于大多数通道病,目前的治疗选择只是对症治疗,仍然缺乏纠正根本损伤的治疗方法。在这种情况下,需要依赖基因和蛋白质治疗的方法。基因治疗可以允许表达功能性蛋白质,只要患病细胞中的细胞机制能够正确折叠并将蛋白质运输到细胞膜。而蛋白质治疗可以允许直接递送功能性蛋白质,只要纯化过程不影响蛋白质功能,并且使用了适当的靶向递送载体。在这篇综述中,我们概述了通道病和现有的对症治疗方法。讨论了主要使用病毒载体的基因治疗方法的现状,接着讨论了纳米医学在蛋白质治疗中的作用,以及纳米医学如何被用于将功能性离子通道递送到患病细胞。