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Ultrastructural sonoporation bio-effects: Comparative study on two human cancer cell lines

机译:超微结构声穿孔的生物效应:两种人类癌细胞系的比较研究

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Sonoporation increases transiently the cell membrane permeability, enabling the therapeutic compounds internalization into the cells. Several investigations reported heterogeneities in the permeabilization and transfection efficacy depending on the ultrasound (US) settings and cell type. Here, we compare the sonoporation effects on two human cell lines, glioblastoma and breast cancer using scanning electron microscopy (SEM). Adherent U-87 MG and MDA-MB-231 cells were insonated at 1 W/cm2, during 60 s at 10% or 20% duty cycle, in the presence of BR14® microbubbles, added at a microbubble-cell ratio of 5. SYTOX® Green, a non-permeant fluorescent dye was used at 1μM, to quantify the membrane permeabilization using flow cytometry. The ultrastructural changes of the cell membrane morphology were monitored by SEM. Flow cytometry results show that the percentage of permeabilized U-87 MG cells reaches 60%, while this value doesn't exceed 40% for MDA-MB-231 cells. These results indicate that the percentage of permeabilized cells depends on the cell type. SEM observations were carried out to elucidate the differences in permeabilization rate between the two cell lines. The SEM analysis reveals that control cells show regular plasma membrane morphology. Their insonation in the presence of BR14® induce the formation of dark holes on their membrane surfaces (named here pore-like structures). However, the quantitative analysis of the SEM micrographs highlights noticeable differences in morphological changes post-sonoporation between the two cell lines. Thus, the mean number of pore-like structures is more abundant on U-87 MG cell membrane than on MDA-MB-231 cell membrane (645 vs. 290). In addition, the mean size of pore-like structures depends on the cell line. Indeed, the mean size on MDA-MB-231 cells was 40 ± 1.2 nm (30-60 nm) while this value reached 80 ± 0.9 nm (10 to 160 nm) for U-8- MG cells. In conclusion, the study confirms that the pore-like structures observed post sonoporation are directly associated to the cell permeabilization rate. Moreover, the observed differences in the permeabilization levels between both cell lines could be attributed to the differences in the number and size of pore-like structures that were seen on the cell membrane. This difference may be due to the fibroblastic nature of the U-87 MG cells in comparison to MDA-MB-231 cells.
机译:Sonoporation暂时增加了细胞膜的通透性,使治疗性化合物内化到细胞中。几项研究报告了通透性和转染效率的异质性,具体取决于超声(US)设置和细胞类型。在这里,我们使用扫描电子显微镜(SEM)比较了声穿孔对两种人类细胞胶质母细胞瘤和乳腺癌的影响。在存在BR14 ®< / sup>微泡,以5的微泡/泡比添加。使用非渗透性荧光染料SYTOX Green,以1μM的浓度使用流式细胞仪定量膜的通透性。通过SEM监测细胞膜形态的超微结构变化。流式细胞仪结果表明,透化的U-87 MG细胞百分比达到60%,而MDA-MB-231细胞的这一值不超过40%。这些结果表明,透化细胞的百分比取决于细胞类型。进行SEM观察以阐明两种细胞系之间透化率的差异。 SEM分析表明,对照细胞显示出规则的质膜形态。在存在BR14 ®的情况下,它们的共鸣会诱导在其膜表面上形成黑洞(此处称为孔状结构)。但是,SEM显微照片的定量分析突出显示了两种细胞系在sonoporation后形态变化的显着差异。因此,U-87 MG细胞膜上的孔状结构的平均数目比MDA-MB-231细胞膜上的平均数目要多(645对290)。另外,孔状结构的平均大小取决于细胞系。实际上,MDA-MB-231细胞的平均大小为40±1.2 nm(30-60 nm),而U-8-MG细胞的平均大小为80±0.9 nm(10至160 nm)。总之,该研究证实了在声穿孔后观察到的孔状结构与细胞通透率直接相关。此外,观察到的两种细胞系之间通透性水平的差异可以归因于在细胞膜上看到的孔状结构的数量和大小的差异。这种差异可能是由于与MDA-MB-231细胞相比,U-87 MG细胞具有成纤维细胞特性。

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