Department of Chemical Engineering, National Chung Cheng University, Chia-Yi, Taiwan.
Electrophoresis. 2010 Jan;31(2):315-23. doi: 10.1002/elps.200900336.
This study analyzes the varying electrophoretic mobility and zeta potential of bone marrow stromal cells (BMSCs) during their differentiation towards neurons. Electrophoresis of primary BMSCs and neuron growth factor (NGF)-induced neuron-like cells with the uptake of heparin-functionalized poly(lactide-co-glycolide) (PLGA) nanoparticles (NPs) are also investigated. Immunofluorescent images revealed that a high concentration of NGF accelerated the differentiation of BMSCs into neurons. When the concentration of NGF increased, the absolute values of electrophoretic mobility and zeta potential of the differentiating BMSCs increased. In addition, a longer inductive period yielded higher charge of the differentiating BMSCs and a smaller uptake amount of heparin-functionalized PLGA NPs. However, an increase in the loading efficiency of heparin on PLGA NPs enhanced the uptake and reduced the electrical characteristics of the primary and differentiating BMSCs. Hence, a general rule is drawn that an increase in the uptake of heparin-functionalized PLGA NPs decreased the electrophoretic mobility and zeta potential of BMSCs during differentiation towards neurons.
本研究分析了骨髓基质细胞(BMSCs)在向神经元分化过程中的电泳迁移率和zeta 电位的变化。还研究了肝素功能化聚(乳酸-共-乙醇酸)(PLGA)纳米颗粒(NPs)摄取后,原代 BMSCs 和神经生长因子(NGF)诱导的类神经元细胞的电泳。免疫荧光图像显示,高浓度的 NGF 加速了 BMSCs 向神经元的分化。随着 NGF 浓度的增加,分化的 BMSCs 的电泳迁移率和 zeta 电位的绝对值增加。此外,诱导时间延长会使分化的 BMSCs 的电荷量增加,肝素功能化 PLGA NPs 的摄取量减少。然而,肝素在 PLGA NPs 上的载药量增加会增强摄取并降低原代和分化的 BMSCs 的电特性。因此,得出一个普遍规律,即肝素功能化 PLGA NPs 的摄取增加会降低向神经元分化过程中 BMSCs 的电泳迁移率和 zeta 电位。