IEEE Trans Nanobioscience. 2016 Jul;15(5):398-411. doi: 10.1109/TNB.2016.2547639. Epub 2016 Mar 28.
Cell mechanics has been proved to be an effective biomarker for indicating cellular states. The advent of atomic force microscopy (AFM) provides an exciting instrument for measuring the mechanical properties of single cells. However, current AFM single-cell mechanical measurements are commonly performed on cell lines cultured in vitro which are quite different from the primary cells in the human body. Investigating the mechanical properties of primary cells from clinical environments can help us to better understand cell behaviors. Here, by combining AFM with magnetic beads cell isolation, the viscoelastic properties of human primary B lymphocytes were quantitatively measured. B lymphocytes were isolated from the peripheral blood of healthy volunteers by density gradient centrifugation and CD19 magnetic beads cell isolation. The activity and specificity of the isolated cells were confirmed by fluorescence microscopy. AFM imaging revealed the surface topography and geometric parameters of B lymphocytes. The instantaneous modulus and relaxation time of living B lymphocytes were measured by AFM indenting technique, showing that the instantaneous modulus of human normal B lymphocytes was 2-3 kPa and the relaxation times were 0.03-0.06 s and 0.35-0.55 s. The differences in cellular visocoelastic properties between primary B lymphocytes and cell lines cultured in vitro were analyzed. The study proves the capability of AFM in quantifying the viscoelastic properties of individual specific primary cells from the blood sample of clinical patients, which will improve our understanding of the behaviors of cells in the human body.
细胞力学已被证明是一种用于指示细胞状态的有效生物标志物。原子力显微镜(AFM)的出现为测量单细胞的力学特性提供了一种令人兴奋的仪器。然而,目前的AFM单细胞力学测量通常是在体外培养的细胞系上进行的,这些细胞系与人体中的原代细胞有很大不同。研究临床环境中原代细胞的力学特性有助于我们更好地理解细胞行为。在此,通过将AFM与磁珠细胞分离相结合,定量测量了人原代B淋巴细胞的粘弹性特性。通过密度梯度离心和CD19磁珠细胞分离从健康志愿者的外周血中分离出B淋巴细胞。通过荧光显微镜确认分离细胞的活性和特异性。AFM成像揭示了B淋巴细胞的表面形貌和几何参数。通过AFM压痕技术测量了活B淋巴细胞的瞬时模量和弛豫时间,结果表明人正常B淋巴细胞的瞬时模量为2-3 kPa,弛豫时间分别为0.03-0.06 s和0.35-0.55 s。分析了原代B淋巴细胞与体外培养的细胞系之间细胞粘弹性特性的差异。该研究证明了AFM在定量临床患者血样中单个特定原代细胞的粘弹性特性方面的能力,这将增进我们对人体细胞行为的理解。