Ketpun Dettachai, Sailasuta Achariya, Suwannaphan Thammawit, Bhanpattanakul Sudchaya, Pimpin Alongkorn, Srituravanich Werayut, Sripumkhai Witsaroot, Jeamsaksiri Wutthinan, Piyaviriyakul Prapruddee
Biochemistry Unit, Department of Physiology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok 10330, Thailand.
Companion Animal Cancer-Research Unit (CAC-RU), Department of Pathology, Faculty of Veterinary Science, Chulalongkorn University, Bangkok 10330, Thailand.
Micromachines (Basel). 2017 Dec 28;9(1):9. doi: 10.3390/mi9010009.
Our laboratory has the fundamental responsibility to study cancer stem cells (CSC) in various models of human and animal neoplasms. However, the major impediments that spike our accomplishment are the lack of universal biomarkers and cellular heterogeneity. To cope with these restrictions, we have tried to apply the concept of single cell analysis, which has hitherto been recommended throughout the world as an imperative solution pack for resolving such dilemmas. Accordingly, our first step was to utilize a predesigned spiral microchannel fabricated by our laboratory to perform size-based single cell separation using mast cell tumor (MCT) cells as a model. However, the impact of hydrodynamic shear stresses (HSS) on mechanical cell injury and viability in a spiral microchannel has not been fully investigated so far. Intuitively, our computational fluid dynamics (CFD) simulation has strongly revealed the formations of fluid shear stress (FSS) and extensional fluid stress (EFS) in the sorting system. The panel of biomedical assays has also disclosed cell degeneration and necrosis in the model. Therefore, we have herein reported the combinatorically detrimental effect of FSS and EFS on the viability of MCT cells after sorting in our spiral microchannel, with discussion on the possibly pathogenic mechanisms of HSS-induced cell injury in the study model.
我们实验室肩负着在各种人类和动物肿瘤模型中研究癌症干细胞(CSC)的基本责任。然而,阻碍我们取得成果的主要因素是缺乏通用生物标志物和细胞异质性。为应对这些限制,我们尝试应用单细胞分析概念,该概念在全球范围内一直被推荐为解决此类困境的必要解决方案。因此,我们的第一步是利用我们实验室制造的预先设计的螺旋微通道,以肥大细胞瘤(MCT)细胞为模型进行基于大小的单细胞分离。然而,到目前为止,流体动力剪切应力(HSS)对螺旋微通道中细胞机械损伤和活力的影响尚未得到充分研究。直观地说,我们的计算流体动力学(CFD)模拟有力地揭示了分选系统中流体剪切应力(FSS)和拉伸流体应力(EFS)的形成。生物医学检测小组也揭示了该模型中的细胞变性和坏死。因此,我们在此报告了FSS和EFS对我们螺旋微通道中分选后MCT细胞活力的联合有害作用,并讨论了研究模型中HSS诱导细胞损伤的可能致病机制。