Rotan Olga, Severin Katharina N, Pöpsel Simon, Peetsch Alexander, Merdanovic Melisa, Ehrmann Michael, Epple Matthias
Inorganic Chemistry and Center for Nanointegration Duisburg-Essen (CeNIDE), University of Duisburg-Essen, Universitaetsstr. 5-7, D-45117 Essen, Germany.
Centre for Medical Biotechnology, Faculty of Biology, University of Duisburg-Essen, Universitaetsstr. 5-7, D-45117 Essen, Germany.
Beilstein J Nanotechnol. 2017 Feb 7;8:381-393. doi: 10.3762/bjnano.8.40. eCollection 2017.
The efficient intracellular delivery of (bio)molecules into living cells remains a challenge in biomedicine. Many biomolecules and synthetic drugs are not able to cross the cell membrane, which is a problem if an intracellular mode of action is desired, for example, with a nuclear receptor. Calcium phosphate nanoparticles can serve as carriers for small and large biomolecules as well as for synthetic compounds. The nanoparticles were prepared and colloidally stabilized with either polyethyleneimine (PEI; cationic nanoparticles) or carboxymethyl cellulose (CMC; anionic nanoparticles) and loaded with defined amounts of the fluorescently labelled proteins HTRA1, HTRA2, and BSA. The nanoparticles were purified by ultracentrifugation and characterized by dynamic light scattering and scanning electron microscopy. Various cell types (HeLa, MG-63, THP-1, and hMSC) were incubated with fluorescently labelled proteins alone or with protein-loaded cationic and anionic nanoparticles. The cellular uptake was followed by light and fluorescence microscopy, confocal laser scanning microscopy (CLSM), and flow cytometry. All proteins were readily transported into the cells by cationic calcium phosphate nanoparticles. Notably, only HTRA1 was able to penetrate the cell membrane of MG-63 cells in dissolved form. However, the application of endocytosis inhibitors revealed that the uptake pathway was different for dissolved HTRA1 and HTRA1-loaded nanoparticles.
在生物医学中,将(生物)分子高效地细胞内递送仍是一项挑战。许多生物分子和合成药物无法穿过细胞膜,如果期望细胞内作用模式,例如作用于核受体时,这就是个问题。磷酸钙纳米颗粒可作为大小生物分子以及合成化合物的载体。通过聚乙烯亚胺(PEI;阳离子纳米颗粒)或羧甲基纤维素(CMC;阴离子纳米颗粒)制备纳米颗粒并使其胶体稳定化,然后装载一定量荧光标记的蛋白质HTRA1、HTRA2和牛血清白蛋白(BSA)。通过超速离心纯化纳米颗粒,并通过动态光散射和扫描电子显微镜对其进行表征。将各种细胞类型(HeLa、MG - 63、THP - 1和人间充质干细胞(hMSC))与单独的荧光标记蛋白质或与装载蛋白质的阳离子和阴离子纳米颗粒一起孵育。通过光学显微镜、荧光显微镜、共聚焦激光扫描显微镜(CLSM)和流式细胞术追踪细胞摄取情况。所有蛋白质都能通过阳离子磷酸钙纳米颗粒轻松转运到细胞中。值得注意的是,只有HTRA1能够以溶解形式穿透MG - 63细胞的细胞膜。然而,内吞作用抑制剂的应用表明,溶解的HTRA1和装载HTRA1的纳米颗粒的摄取途径不同。