Lulevich Valentin, Shih Yi-Ping, Lo Su Hao, Liu Gang-Yu
Department of Chemistry, University of California, Davis, California 95616, USA.
J Phys Chem B. 2009 May 7;113(18):6511-9. doi: 10.1021/jp8103358.
Cell tracing dyes are very frequently utilized in cellular biology research because they provide highly sensitive fluorescent tags that do not compromise cellular functions such as growth and proliferation. In many investigations concerning cellular adhesion and mechanics, fluorescent dyes have been employed with the assumption of little impact on the results. Using the single cell compression technique developed by our team, the single cell mechanics of MDA-MB-468 and MLC-SV40 cells were investigated as a function of dye uptake. Cell tracing dyes increase living cell stiffness 3-6 times and cell-to-probe adhesion up to 7 times. These results suggest a more significant effect than toxins, such as thrombin. A simple analytical model was derived to enable the extraction of the Young's moduli of the cell membrane and cytoskeleton from the force-deformation profiles measured for individual cells. The increase in Young's modulus of the membrane is 3-7 times, which is more significant than that of the cytoskeleton (1.1-3.4 times). We propose that changes in cell mechanics upon the addition of fluorescent tracing dye are primarily due to the incorporation of amphiphilic dye molecules into the cellular plasma membrane, which increases the lateral interaction among phospholipid chains and thus enhances their rigidity and adhesion.
细胞追踪染料在细胞生物学研究中被频繁使用,因为它们提供了高度敏感的荧光标记,且不会损害细胞功能,如生长和增殖。在许多关于细胞黏附和力学的研究中,荧光染料的使用基于对结果影响很小的假设。利用我们团队开发的单细胞压缩技术,研究了MDA-MB-468和MLC-SV40细胞的单细胞力学与染料摄取的关系。细胞追踪染料使活细胞硬度增加3至6倍,细胞与探针的黏附力增加高达7倍。这些结果表明其作用比凝血酶等毒素更为显著。推导了一个简单的分析模型,以便从单个细胞测量的力-变形曲线中提取细胞膜和细胞骨架的杨氏模量。膜的杨氏模量增加了3至7倍,比细胞骨架的增加更为显著(1.1至3.4倍)。我们认为,添加荧光追踪染料后细胞力学的变化主要是由于两亲性染料分子掺入细胞质膜,这增加了磷脂链之间的横向相互作用,从而提高了它们的刚性和黏附力。