Liu Qiaoling, Bi Cheng, Li Jiangling, Liu Xuejiao, Peng Ruizi, Jin Cheng, Sun Yang, Lyu Yifan, Liu Hui, Wang Huijing, Luo Can, Tan Weihong
Molecular Science and Biomedicine Laboratory (MBL), State Key Laboratory of Chemo/Bio-Sensing and Chemometrics, College of Biology, College of Chemistry and Chemical Engineering, Aptamer Engineering Center of Hunan Province, Hunan University, Changsha, China.
Institute of Molecular Medicine (IMM), Renji Hospital, Shanghai Jiao Tong University School of Medicine and School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai, China.
Research (Wash D C). 2019 Jun 17;2019:6523970. doi: 10.34133/2019/6523970. eCollection 2019.
Biomimetic giant membrane vesicles, with size and lipid compositions comparable to cells, have been recognized as an attractive experimental alternative to living systems. Due to the similarity of their membrane structure to that of body cells, cell-derived giant plasma membrane vesicles have been used as a membrane model for studying lipid/protein behavior of plasma membranes. However, further application of biomimetic giant membrane vesicles has been hampered by the side-effects of chemical vesiculants and the utilization of osmotic buffer. We herein develop a facile strategy to derive giant membrane vesicles (GMVs) from mammalian cells in biofriendly medium with high yields. These GMVs preserve membrane properties and adaptability for surface modification and encapsulation of exogenous molecules, which would facilitate their potential biological applications. Moreover, by loading GMVs with therapeutic drugs, GMVs could be employed for drug transport to tumor cells, which represents another step forward in the biomedical application of giant membrane vesicles. This study highlights biocompatible GMVs with biomimicking membrane surface properties and adaptability as an ideal platform for drug delivery strategies with potential clinical applications.
仿生巨型膜泡的大小和脂质组成与细胞相当,已被认为是一种替代活细胞系统的有吸引力的实验选择。由于其膜结构与体细胞相似,细胞来源的巨型质膜泡已被用作研究质膜脂质/蛋白质行为的膜模型。然而,化学囊泡剂的副作用和渗透缓冲液的使用阻碍了仿生巨型膜泡的进一步应用。我们在此开发了一种简便的策略,可在生物友好型培养基中从哺乳动物细胞高产率地获得巨型膜泡(GMV)。这些GMV保留了膜特性以及对外源分子进行表面修饰和包封的适应性,这将促进它们潜在的生物学应用。此外,通过在GMV中装载治疗药物,GMV可用于将药物运输到肿瘤细胞,这代表了巨型膜泡在生物医学应用中的又一进展。本研究强调了具有仿生膜表面特性和适应性的生物相容性GMV,作为具有潜在临床应用的药物递送策略的理想平台。