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Adhesion of melanoma cells to the surfaces of microspheres studied by atomic force microscopy.

机译:通过原子力显微镜研究黑色素瘤细胞对微球表面的粘附。

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摘要

It is of fundamental importance to understand the mechanism of adhesion between a mammalian cell and a material surface. In the present study, we have used atomic force microscopy (AFM) to measure the interaction forces between the murine melanoma cells and the single polystyrene microspheres of different surface chemistries in serum-free culture media: the unmodified hydrophobic polystyrene (bare/PS) and the carboxyl-modified polystyrene (COOH/PS). The cell-microsphere interaction forces have been also measured in the culture media containing the free Arg-Gly-Asp (RGD) peptides as an integrin inhibitor. In the absence of free RGD peptides, the adhesion force for COOH/PS was larger than that for bare/PS. The adhesion force for COOH/PS decreased with increasing the concentration of free RGD peptides added in the culture media and then became almost constant at the RGD concentrations larger than 0.5 mg/mL, whereas that for bare/PS remained very small regardless of the RGD concentration. In addition, the effects of the microsphere diameter and the contact time on the adhesion forces were investigated. On the basis of the AFM results, possible mechanism of cell-microsphere adhesion will be discussed.
机译:了解哺乳动物细胞与材料表面之间的粘附机制至关重要。在本研究中,我们使用原子力显微镜(AFM)来测量无血清培养基中鼠黑素瘤细胞与不同表面化学物质的单个聚苯乙烯微球之间的相互作用力:未改性的疏水聚苯乙烯(裸/ PS)和羧基改性的聚苯乙烯(COOH / PS)。还已在含有游离Arg-Gly-Asp(RGD)肽作为整联蛋白抑制剂的培养基中测量了细胞-微球相互作用力。在没有游离RGD肽的情况​​下,COOH / PS的粘附力大于裸露/ PS的粘附力。 COOH / PS的粘附力随培养基中游离RGD肽浓度的增加而降低,然后在RGD浓度大于0.5 mg / mL时几乎保持恒定,而裸露/ PS的粘附力却很小,而与RGD无关浓度。另外,研究了微球直径和接触时间对粘附力的影响。根据原子力显微镜的结果,将讨论细胞微球粘附的可能机理。

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