Maeki Masatoshi, Niwa Ayuka, Oyama Shota, Aratani Kyoko, Ito Rina, Suzuki Yuichi, Sato Yusuke, Ishida Akihiko, Harashima Hideyoshi, Tokeshi Manabu
Division of Applied Chemistry, Faculty of Engineering, Hokkaido University, Kita 13 Nishi 8, Kita-ku, Sapporo 060-8628, Japan.
Graduate School of Chemical Sciences and Engineering, Hokkaido University, Kita 13 Nishi 8, Kita-ku, Sapporo 060-8628, Japan.
ACS Appl Mater Interfaces. 2025 Jul 23;17(29):41666-41679. doi: 10.1021/acsami.5c06927. Epub 2025 Jun 16.
Exosomes, which are cell-secreted lipid-based nanoparticles, play a crucial role in intercellular communication by encapsulating and delivering various biomolecules such as DNA, mRNA, miRNA, and proteins. They offer potential as drug delivery systems (DDSs) based on their ability to cross biological barriers, use natural communication mechanisms, and minimize immunogenicity. However, the heterogeneity of exosomes presents a bottleneck for functional analysis and the development of exosome-based DDSs. Therefore, engineering techniques are needed to produce exosomes or exosome-mimicking nanoparticles with controlled characteristics, including the presentation of specific exosomal proteins on their surface. Here, a one-step microfluidic method for producing exosome-mimicking lipid-based nanoparticles decorated with specific exosomal proteins was developed, enabling control over the composition and characteristics of the resulting exosomes. Exosome-mimicking nanoparticles decorated with tetraspanin proteins (CD9, CD63, CD81) and integrins (ITG αVβ5, ITG α6β4), which are involved in cell signaling and organ targeting, were thereby generated. Investigating the impact of these exosomal proteins on RNA delivery efficiency revealed that ITG αVβ5-decorated exosome-mimicking nanoparticles significantly enhance RNA delivery both in vitro and in vivo. This study provides an approach for producing precisely decorated exosome-mimicking nanoparticles, which may be applied to elucidate the functions of exosomal proteins and develop targeted DDSs.
外泌体是细胞分泌的基于脂质的纳米颗粒,通过包裹和传递各种生物分子(如DNA、mRNA、miRNA和蛋白质)在细胞间通讯中发挥关键作用。基于其穿越生物屏障的能力、利用天然通讯机制以及最小化免疫原性的特点,外泌体有望成为药物递送系统(DDS)。然而,外泌体的异质性为功能分析和基于外泌体的DDS的开发带来了瓶颈。因此,需要工程技术来生产具有可控特性的外泌体或外泌体模拟纳米颗粒,包括在其表面呈现特定的外泌体蛋白。在此,开发了一种一步微流控方法,用于生产装饰有特定外泌体蛋白的外泌体模拟脂质纳米颗粒,从而能够控制所得外泌体的组成和特性。由此产生了装饰有参与细胞信号传导和器官靶向的四跨膜蛋白(CD9、CD63、CD81)和整合素(ITGαVβ5、ITGα6β4)的外泌体模拟纳米颗粒。研究这些外泌体蛋白对RNA递送效率的影响表明,装饰有ITGαVβ5的外泌体模拟纳米颗粒在体外和体内均显著提高RNA递送效率。本研究提供了一种生产精确装饰的外泌体模拟纳米颗粒的方法,可用于阐明外泌体蛋白的功能并开发靶向DDS。