Li Hua, Tsui Tung Yu, Ma Wenxue
Department of Basic Medical Science, Huzhou University School of Medicine, Huzhou 313000, China.
Department of General, Visceral and Thoracic Surgery, University Medical Center Hamburg-Eppendorf, Martinistr. 52, 20246 Hamburg, Germany.
Int J Mol Sci. 2015 Aug 18;16(8):19518-36. doi: 10.3390/ijms160819518.
Cell-penetrating peptides (CPPs) can cross cellular membranes in a non-toxic fashion, improving the intracellular delivery of various molecular cargos such as nanoparticles, small molecules and plasmid DNA. Because CPPs provide a safe, efficient, and non-invasive mode of transport for various cargos into cells, they have been developed as vectors for the delivery of genetic and biologic products in recent years. Most common CPPs are positively charged peptides. While delivering negatively charged molecules (e.g., nucleic acids) to target cells, the internalization efficiency of CPPs is reduced and inhibited because the cationic charges on the CPPs are neutralized through the covering of CPPs by cargos on the structure. Even under these circumstances, the CPPs can still be non-covalently complexed with the negatively charged molecules. To address this issue, combination strategies of CPPs with other typical carriers provide a promising and novel delivery system. This review summarizes the latest research work in using CPPs combined with molecular cargos including liposomes, polymers, cationic peptides, nanoparticles, adeno-associated virus (AAV) and calcium for the delivery of genetic products, especially for small interfering RNA (siRNA). This combination strategy remedies the reduced internalization efficiency caused by neutralization.
细胞穿透肽(CPPs)能够以无毒方式穿过细胞膜,提高各种分子货物(如纳米颗粒、小分子和质粒DNA)的细胞内递送效率。由于CPPs为各种货物进入细胞提供了一种安全、高效且非侵入性的运输方式,近年来它们已被开发为递送基因和生物制品的载体。最常见的CPPs是带正电荷的肽。在将带负电荷的分子(如核酸)递送至靶细胞时,CPPs的内化效率会降低并受到抑制,因为CPPs上的阳离子电荷会通过结构上的货物覆盖CPPs而被中和。即使在这种情况下,CPPs仍可与带负电荷的分子非共价复合。为了解决这个问题,CPPs与其他典型载体的联合策略提供了一种有前景的新型递送系统。本综述总结了使用CPPs与包括脂质体、聚合物、阳离子肽、纳米颗粒、腺相关病毒(AAV)和钙在内的分子货物联合用于递送基因产物,特别是小干扰RNA(siRNA)的最新研究工作。这种联合策略弥补了中和作用导致的内化效率降低的问题。