Department of Nanomedicine & Drug Targeting, Groningen Research Institute of Pharmacy, University of Groningen, Groningen, The Netherlands.
Department of Nanomedicine & Drug Targeting, Groningen Research Institute of Pharmacy, University of Groningen, Groningen, The Netherlands.
Nanomedicine. 2020 Nov;30:102300. doi: 10.1016/j.nano.2020.102300. Epub 2020 Sep 12.
Zwitterionic molecules are used as an alternative to PEGylation to reduce protein adsorption on nanocarriers. Nonetheless, little is known on the effect of zwitterionic modifications on the mechanisms cells use for nanocarrier uptake. In this study, the uptake mechanism of liposomes containing zwitterionic or negatively charged lipids was characterized using pharmacological inhibitors and RNA interference on HeLa cells to block endocytosis. As expected, introducing zwitterionic lipids reduced protein adsorption in serum, as well as uptake efficiency. Blocking clathrin-mediated endocytosis strongly decreased the uptake of the negatively charged liposomes, but not the zwitterionic ones. Additionally, inhibition of macropinocytosis reduced uptake of both liposomes, but blocking actin polymerization had effects only on the negatively charged ones. Overall, the results clearly indicated that the two liposomes were internalized by HeLa cells using different pathways. Thus, introducing zwitterionic lipids affects not only protein adsorption and uptake efficiency, but also the mechanisms of liposome uptake by cells.
两性离子分子被用作聚乙二醇化的替代品,以减少纳米载体上蛋白质的吸附。尽管如此,关于两性离子修饰对细胞摄取纳米载体的机制的影响,人们知之甚少。在这项研究中,使用 HeLa 细胞中的药理学抑制剂和 RNA 干扰来阻断内吞作用,对含有两性离子或负电荷脂质的脂质体的摄取机制进行了表征。正如预期的那样,引入两性离子脂质可减少血清中的蛋白质吸附以及摄取效率。网格蛋白介导的内吞作用的阻断强烈降低了带负电荷的脂质体的摄取,但对两性离子脂质体没有影响。此外,巨胞饮作用的抑制均降低了两种脂质体的摄取,但肌动蛋白聚合的阻断仅对带负电荷的脂质体有影响。总的来说,结果清楚地表明,两种脂质体均通过不同途径被 HeLa 细胞内化。因此,引入两性离子脂质不仅会影响蛋白质吸附和摄取效率,还会影响细胞摄取脂质体的机制。