Teramura Yuji, Kaneda Yoshihiro, Totani Takahiko, Iwata Hiroo
Department of Nano-Medicine Merger Education Unit, Kyoto University, 53 Kawara-cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.
Biomaterials. 2008 Apr;29(10):1345-55. doi: 10.1016/j.biomaterials.2007.11.048. Epub 2008 Jan 11.
We used three kinds of polymers that interact with living cells in different modes: poly(ethylene glycol)-conjugated phospholipid (PEG-lipid) and poly(vinyl alcohol) carrying alkyl side chains (PVA-alkyl), expected to anchor to the membrane lipid bilayer through hydrophobic interactions; N-hydroxysuccinimidyl-PEG (PEG-NHS), which covalently bonds with all kinds of membrane proteins having amino groups on cell surfaces; and polyelectrolytes, poly(ethylene imine) (PEI) and carboxylated PVA (PVA-COOH), which interact with cells electrostatically. CCRF-CEM (T-cell like) and HEK293 (adherent cell) cell lines were used. We followed the surface dynamics of fluorescently labeled polymers on living cells over time using confocal laser scanning microscopy and flow cytometry. PEI destroyed cells, while PVA-COOH did not interact with cells. PEG-lipid, PVA-alkyl, and PEG-NHS interacted with cells without cytotoxicity and existed on the cell surface even after cells were washed. PEG-lipid and PEG-NHS were rapidly excluded from the cell surface without cytoplasmic uptake, while PVA-alkyl assembled on the living cell surface was taken into the cytoplasm and then excluded. Most polymers were excluded within 24h although exclusion routes seemed to be different between polymers, suggesting that cell transplant surface modifications are shorter than has been assumed. The short life of modified polymers on the cell surface should be a consideration for cell transplant surface modifications.
聚(乙二醇)共轭磷脂(PEG-脂质)和带有烷基侧链的聚乙烯醇(PVA-烷基),预计它们会通过疏水相互作用锚定在膜脂双层上;N-羟基琥珀酰亚胺-PEG(PEG-NHS),它能与细胞表面带有氨基的各种膜蛋白共价结合;以及聚电解质,聚乙烯亚胺(PEI)和羧化聚乙烯醇(PVA-COOH),它们通过静电作用与细胞相互作用。使用了CCRF-CEM(T细胞样)和HEK293(贴壁细胞)细胞系。我们使用共聚焦激光扫描显微镜和流式细胞术,随时间跟踪荧光标记聚合物在活细胞上的表面动态。PEI会破坏细胞,而PVA-COOH不与细胞相互作用。PEG-脂质、PVA-烷基和PEG-NHS与细胞相互作用且无细胞毒性,即使在细胞洗涤后仍存在于细胞表面。PEG-脂质和PEG-NHS迅速从细胞表面被排除,未被胞质摄取,而组装在活细胞表面的PVA-烷基则被摄入细胞质然后被排除。尽管不同聚合物的排除途径似乎不同,但大多数聚合物在24小时内被排除,这表明细胞移植表面修饰的持续时间比之前设想的要短。细胞表面修饰聚合物的短寿命在细胞移植表面修饰时应予以考虑。