Neuronal Survival Unit, Department of Experimental Medical Science, Wallenberg Neuroscience Center, Lund University, Lund, Sweden.
PLoS One. 2013 May 27;8(5):e64233. doi: 10.1371/journal.pone.0064233. Print 2013.
The use of acoustic forces to manipulate particles or cells at the microfluidic scale (i.e. acoustophoresis), enables non-contact, label-free separation based on intrinsic cell properties such as size, density and compressibility. Acoustophoresis holds great promise as a cell separation technique in several research and clinical areas. However, it has been suggested that the force acting upon cells undergoing acoustophoresis may impact cell viability, proliferation or cell function via subtle phenotypic changes. If this were the case, it would suggest that the acoustophoresis method would be a less useful tool for many cell analysis applications as well as for cell therapy.
We investigate, for the first time, several key aspects of cellular changes following acoustophoretic processing. We used two settings of ultrasonic actuation, one that is used for cell sorting (10 Vpp operating voltage) and one that is close to the maximum of what the system can generate (20 Vpp). We used microglial cells and assessed cell viability and proliferation, as well as the inflammatory response that is indicative of more subtle changes in cellular phenotype. Furthermore, we adapted a similar methodology to monitor the response of human prostate cancer cells to acoustophoretic processing. Lastly, we analyzed the respiratory properties of human leukocytes and thrombocytes to explore if acoustophoretic processing has adverse effects.
BV2 microglia were unaltered after acoustophoretic processing as measured by apoptosis and cell turnover assays as well as inflammatory cytokine response up to 48 h following acoustophoresis. Similarly, we found that acoustophoretic processing neither affected the cell viability of prostate cancer cells nor altered their prostate-specific antigen secretion following androgen receptor activation. Finally, human thrombocytes and leukocytes displayed unaltered mitochondrial respiratory function and integrity after acoustophoretic processing.
We conclude that microchannel acoustophoresis can be used for effective continuous flow-based cell separation without affecting cell viability, proliferation, mitochondrial respiration or inflammatory status.
在微流控尺度上使用声力操纵颗粒或细胞(即声悬浮),可以实现基于细胞固有特性(如大小、密度和可压缩性)的非接触、无标记分离。声悬浮作为一种细胞分离技术,在多个研究和临床领域具有广阔的应用前景。然而,有人认为,细胞在声悬浮过程中所受的力可能会通过微妙的表型变化影响细胞活力、增殖或细胞功能。如果情况确实如此,那么这将表明声悬浮方法对于许多细胞分析应用以及细胞治疗来说,将不再是一个有用的工具。
我们首次研究了细胞在声悬浮处理后发生的几个关键变化方面。我们使用了两种超声激励设置,一种用于细胞分选(10Vpp 工作电压),另一种接近系统所能产生的最大值(20Vpp)。我们使用小神经胶质细胞评估了细胞活力和增殖,以及炎症反应,这表明细胞表型发生了更微妙的变化。此外,我们采用了类似的方法来监测人前列腺癌细胞对声悬浮处理的反应。最后,我们分析了人白细胞和血小板的呼吸特性,以探讨声悬浮处理是否会产生不良影响。
BV2 小神经胶质细胞在声悬浮处理后,通过凋亡和细胞更新测定以及炎症细胞因子反应,在声悬浮处理后 48 小时内没有改变。同样,我们发现,声悬浮处理既不影响前列腺癌细胞的活力,也不改变它们在雄激素受体激活后的前列腺特异性抗原分泌。最后,人血小板和白细胞在声悬浮处理后,线粒体呼吸功能和完整性没有改变。
我们得出结论,微通道声悬浮可以用于有效的连续流细胞分离,而不会影响细胞活力、增殖、线粒体呼吸或炎症状态。