Xavier Miguel, de Andrés María C, Spencer Daniel, Oreffo Richard O C, Morgan Hywel
Faculty of Physical Sciences and Engineering, and Institute for Life Sciences, University of Southampton, Southampton SO17 1BJ, UK.
Centre for Human Development, Stem Cells and Regeneration, Institute of Developmental Sciences, Southampton General Hospital, Tremona Road, SO16 6YD Southampton, UK.
J R Soc Interface. 2017 Aug;14(133). doi: 10.1098/rsif.2017.0233.
The capacity of bone and cartilage to regenerate can be attributed to skeletal stem cells (SSCs) that reside within the bone marrow (BM). Given SSCs are rare and lack specific surface markers, antibody-based sorting has failed to deliver the cell purity required for clinical translation. Microfluidics offers new methods of isolating cells based on biophysical features including, but not limited to, size, electrical properties and stiffness. Here we report the characterization of the dielectric properties of unexpanded SSCs using single-cell microfluidic impedance cytometry (MIC). Unexpanded SSCs had a mean size of 9.0 µm; larger than the majority of BM cells. During expansion, often used to purify and increase the number of SSCs, cell size and membrane capacitance increased significantly, highlighting the importance of characterizing unaltered SSCs. In addition, MIC was used to track the osteogenic differentiation of SSCs and showed an increased membrane capacitance with differentiation. The electrical properties of primary SSCs were indistinct from other BM cells precluding its use as an isolation method. However, the current studies indicate that cell size in combination with another biophysical parameter, such as stiffness, could be used to design label-free devices for sorting SSCs with significant clinical impact.
骨骼和软骨的再生能力可归因于存在于骨髓(BM)中的骨骼干细胞(SSCs)。鉴于SSCs十分稀少且缺乏特异性表面标志物,基于抗体的分选方法无法实现临床转化所需的细胞纯度。微流控技术提供了基于生物物理特征(包括但不限于大小、电学性质和硬度)分离细胞的新方法。在此,我们报告了使用单细胞微流控阻抗细胞术(MIC)对未扩增的SSCs介电特性的表征。未扩增的SSCs平均大小为9.0 µm,大于大多数BM细胞。在常用于纯化和增加SSCs数量的扩增过程中,细胞大小和膜电容显著增加,这突出了表征未改变的SSCs的重要性。此外,MIC被用于追踪SSCs的成骨分化,并显示随着分化膜电容增加。原代SSCs的电学性质与其他BM细胞没有明显差异,这使得它无法用作一种分离方法。然而,目前的研究表明,细胞大小与另一个生物物理参数(如硬度)相结合,可用于设计具有重大临床意义的无标记装置来分选SSCs。