Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP, São Carlos, SP, Brazil.
Instituto Nacional de Ciência e Tecnologia de Bioanalítica, INCTBio, Campinas, SP, Brazil.
Sci Rep. 2017 Sep 5;7(1):10466. doi: 10.1038/s41598-017-11043-0.
This study presents an inexpensive and easy way to produce a microfluidic device that mimics a blood vessel, serving as a start point for cell culture under perfusion, cardiovascular research, and toxicological studies. Endpoint assays (i.e., MTT reduction and NO assays) were used and revealed that the components making up the microchip, which is made of polyester and toner (PT), did not induce cell death or nitric oxide (NO) production. Applying oxygen plasma and fibronectin improved the adhesion and proliferation endothelial cell along the microchannel. As expected, these treatments showed an increase in vascular endothelial growth factor (VEGF-A) concentration profiles, which is correlated with adherence and cell proliferation, thus promoting endothelialization of the device for neovascularization. Regardless the simplicity of the device, our "vein-on-a-chip" mimetic has a potential to serve as a powerful tool for those that demand a rapid microfabrication method in cell biology or organ-on-a-chip research.
本研究提出了一种经济且简便的方法来制作微流控装置,该装置模拟血管,可作为灌流条件下细胞培养、心血管研究和毒理学研究的起点。终点分析(即 MTT 还原和 NO 分析)表明,由聚酯和调色剂(PT)制成的微芯片组件不会诱导细胞死亡或产生一氧化氮(NO)。应用氧等离子体和纤连蛋白可改善沿微通道的内皮细胞的粘附和增殖。正如预期的那样,这些处理方法显示出血管内皮生长因子(VEGF-A)浓度分布的增加,这与粘附和细胞增殖相关,从而促进了设备的血管化以实现新血管生成。尽管该设备很简单,但我们的“芯片上静脉”模型有可能成为那些在细胞生物学或器官芯片研究中需要快速微加工方法的人的有力工具。