首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Assessment of the Effects of Surface Potential on the Kinetics of HEK293T Cell Adhesion Behavior Using a Quartz Crystal Microbalance with Dissipation Monitoring
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Assessment of the Effects of Surface Potential on the Kinetics of HEK293T Cell Adhesion Behavior Using a Quartz Crystal Microbalance with Dissipation Monitoring

机译:评估表面电位对HEK293T细胞粘附性能的影响使用石英晶微观与耗散监测

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Cell adhesion plays a key role in biomaterial development. Self-assembled monolayers (SAMs) provide a convenient and versatile means of modifying surface properties to study how environmental cues affect the cell adhesion process. Serial zeta-potential surfaces can be realized by introducing various ratios of oppositely charged functional groups on a gold surface. A quartz crystal microbalance with dissipation monitoring (QCM-D) has advantages for examining real-time viscoelastic changes on surfaces. This surface sensitive technique can be applied in cell adhesion studies to investigate the cell surface interactions. In this work, HEK293T epithelial cells were used to examine the adhesion kinetics of semiadherent cells on NH2-COOH binary SAM-modified surfaces with serial surface potential. Immunofluorescence staining was used to examine focal adhesion sites after a 4-h cell adhesion process. Combined with optical microscopy, QCM-D was used to record in situ and real-time viscoelastic and morphological changes. It was found that HEK293T cells were prone to spread and form more focal adhesion sites on surfaces with more positive charge (more NH2 groups) but aggregated and remained highly mobile on surfaces with more negative charge (more COOH groups). On NH2-rich surfaces, cells underwent three-phase kinetics during the adhesion process. Initially, cells adhered and spread quickly on the NH2-rich surfaces with little or no extracellular matrix (ECM) by the attractive interaction between the positively charged amine groups and negatively charged cell membrane. The epithelial cells then shrank their filopodia in the second phase to normalize their size. In the final phase, cells underwent ECM remodeling and formed matured ECM. On COOH-rich surfaces, four phases were identified during the cell adhesion process. Initially, due to electrostatic repulsion between the negatively charged cell membrane and surfaces, direct cell adhesion and spreading were restricted. However, ECM was quickly deposited. In the second phase, cells adhered on and interacted with the surface through the ECM layer. In the third phase, cells underwent ECM remodeling, and additional ECM was deposited on the surfaces. Finally, instead of cell surface interactions, the cells aggregated to form cell cell junctions. In summary, the cell adhesion process shifted from direct cell surface interaction to cell-ECM-surface interaction and cell-cell junctions when the surface potential shifted from positive to negative.
机译:细胞粘附在生物材料发育中起着关键作用。自组装的单层(SAMS)提供了一种方便而多功能地改变表面性质,以研究环境提示如何影响细胞粘附过程。通过在金表面上引入相反带电官能团的各种比率,可以实现串联ζ电位表面。具有耗散监测(QCM-D)的石英晶体微稳定具有检查表面上实时粘弹性变化的优点。这种表面敏感技术可以应用于细胞粘附研究,以研究细胞表面相互作用。在这项工作中,HEK293T上皮细胞用于检测具有连续表面电位的NH 2-COOH二元SAM改性表面上半叠细胞的粘附动力学。使用免疫荧光染色在4-H细胞粘合过程后检查局灶性粘附位点。结合光学显微镜,QCM-D用于以原位和实时粘弹性和形态变化进行记录。发现HEK293T细胞容易发生在具有更高阳性电荷(更多NH 2组)的表面上的更多局灶性粘附位点,但在具有更多负电荷(更多COOH基团)的表面上保持高度移动性。在富含NH 2的表面上,细胞在粘合过程中接受三相动力学。最初,通过带正电荷的胺基团和带负电的细胞膜之间的有吸引力的相互作用,细胞粘附并迅速地粘附并迅速地蔓延。通过带正电荷的胺基和带负电的细胞膜的含有细胞外基质(ECM)。然后上皮细胞在第二阶段中缩小它们的氟胶质玉米霉菌,以使其尺寸正常化。在最终阶段,细胞接受ECM重塑和形成成熟的ECM。在富含COOH的表面上,在细胞粘附过程中鉴定了四个相。最初,由于带负电荷的细胞膜和表面之间的静电排斥,限制了直接细胞粘附和扩散。但是,ECM很快存放。在第二阶段,细胞粘附在并通过ECM层与表面相互作用。在第三阶段,细胞接受ECM重塑,并沉积在表面上的另外的ECM。最后,代替细胞表面相互作用,细胞聚集以形成细胞单元结。总之,当表面电位从正到负面移位时,电池粘附过程从直接细胞表面相互作用与细胞 - ECM-表面相互作用和细胞 - 细胞连接。

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