Palmer Christopher P, Mycielska Maria E, Burcu Hakan, Osman Kareem, Collins Timothy, Beckerman Rachel, Perrett Rebecca, Johnson Helen, Aydar Ebru, Djamgoz Mustafa B A
Division of Molecular & Cell Biology, Neuroscience Solutions to Cancer Research Group, Sir Alexander Fleming Building, Imperial College London, London, UK.
Eur Biophys J. 2008 Apr;37(4):359-68. doi: 10.1007/s00249-007-0219-2. Epub 2007 Sep 19.
We have developed a simple yet effective apparatus, based upon negative pressure directed to the tip of a micro-pipette, to measure the adhesiveness of single cells. The "single cell adhesion measuring apparatus" (SCAMA) could differentiate between the adhesion of strongly versus weakly metastatic cancer cells as well as normal cells. Adhesion was quantified as "detachment negative pressure" (DNP) or "DNP relative to cell size" (DNPR) where a noticeable difference in cell size was apparent. Thus, for rat and human prostate and human breast cancer cell lines, adhesiveness (DNPR values) decreased in line with increased metastatic potential. Using the SCAMA, we investigated the effect of tetrodotoxin (TTX), a specific blocker of voltage-gated Na(+) channels (VGSCs), on the adhesion of rat and human prostate cancer cell lines of markedly different metastatic potential. Following pretreatment with TTX (48 h with 1 microM), the adhesion values for the Mat-LyLu cells increased significantly 4.3-fold; there was no effect on the AT-2 cells. For the strongly metastatic PC-3M cells, TTX treatment caused a significant (approximately 30%) increase in adhesion. The adhesion of PNT2-C2 ("normal") cells was not affected by the TTX pretreatment. The TTX-induced increase in the adhesiveness of the strongly metastatic cells was consistent with the functional VGSC expression in these cells and the proposed role of VGSC activity in metastatic cell behaviour. In conclusion, the SCAMA, which can be constructed easily and cheaply, offers a simple and effective method to characterise single-cell adhesion and its modulation.
我们开发了一种基于微移液器尖端负压的简单而有效的装置,用于测量单细胞的粘附性。“单细胞粘附测量装置”(SCAMA)能够区分强转移性癌细胞与弱转移性癌细胞以及正常细胞的粘附情况。当细胞大小存在明显差异时,粘附性被量化为“脱离负压”(DNP)或“相对于细胞大小的DNP”(DNPR)。因此,对于大鼠和人类前列腺癌细胞系以及人类乳腺癌细胞系,粘附性(DNPR值)随着转移潜能的增加而降低。我们使用SCAMA研究了河豚毒素(TTX)——一种电压门控钠通道(VGSCs)的特异性阻滞剂——对具有明显不同转移潜能的大鼠和人类前列腺癌细胞系粘附性的影响。用TTX(1 microM,处理48小时)预处理后,Mat-LyLu细胞的粘附值显著增加了4.3倍;对AT-2细胞没有影响。对于强转移性PC-3M细胞,TTX处理导致粘附性显著增加(约30%)。PNT2-C2(“正常”)细胞的粘附性不受TTX预处理的影响。TTX诱导的强转移性细胞粘附性增加与这些细胞中功能性VGSC的表达以及VGSC活性在转移细胞行为中的作用一致。总之,SCAMA构建简单且成本低廉,提供了一种表征单细胞粘附及其调节的简单有效方法。