微流控芯片中细胞迁移效应的研究

Y. Lin, Wenting Liu, Chunfei Hu
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引用次数: 6

摘要

微流控芯片提供了独特的机会来建立新颖的体外细胞模型,其中体内细胞微环境可以精确地重建。虽然它们在细胞生物学领域具有重要意义,但实际应用受到细胞培养环境材料的极大限制,即细胞形态和迁移受底物材料的影响很大。在本研究中,我们研究了四种相同几何形状的微流控芯片对细胞迁移的影响。分别为粘接在培养皿、玻片、PDMS基板上的PDMS模具结构,以及粘接在PMMA基板上的PMMA模具结构。为了便于描述,我们将这四种芯片分别表示为PDMS-DISH、PDMS-GLASS、PDMS-PDMS和PMMA-PMMA。我们比较和总结了细胞在不同基质上迁移效应的关系。细胞最初被引入培养区。实验结果表明,细胞在这些芯片上的扩散时间、扩散面积和细胞迁移具有明显的差异性。为了进一步研究细胞在这些芯片中的迁移,我们用胰蛋白酶/EDTA溶液和细胞培养基制备了一个新的模型。它显示出良好的可重复性。在这些微流控芯片中,大多数细胞能形成良好的形态和单层生长。监测24小时后,细胞在PDMS-DISH芯片中迁移最远。PDMS-DISH、PDMS-GLASS、PDMS-PDMS和PMMA-PMMA的迁移速率分别为20.30 μm/h、18.63 μm/h、15.00 μm/h和10.75 μm/h。这项研究为新型生物芯片在伤口愈合和抗疤痕方面的应用开辟了新的机会,有望在药物筛选和相关领域得到应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigation of Cells Migration Effects in Microfluidic Chips
Microfluidic chips offer the unique opportunity to establish novelty in vitro cells models where the in vivo cells microenvironment could be precisely reconstituted. Although they have significances in the fields of cell biology, the real applications are extremely limited by ambient materials for cells culture, i.e., cells morphology and migration are greatly influenced by substrate material. In this study, we investigated the cells migration effects in four kinds of microfluidic chips with the same geometry. They are PDMS mold structures bonded on culture dish, glass slide, and PDMS substrates, respectively, and another PMMA mold structure bonded on PMMA substrate. For convenient description, we denoted these four chips as PDMS-DISH, PDMS-GLASS, PDMS-PDMS, and PMMA-PMMA, respectively. We compared and summarized the relationship of cells migration effects on different substrate. The cells are initially introduced into the culture area. The experiment results indicate that cells spreading time, spreading area and cells migration on these chips has obvious diversities. To further investigate the cells migration in these chips, a new model is prepared using trypsin/EDTA solution and cell culture medium. It shows a good repeatability. Most of cells could be formed a good morphology and monolayer growth in these microfluidic chips. The cells migrated furthest is in the PDMS-DISH chip after monitored 24 hours. The migration rates are 20.30 μm/h, 18.63 μm/h, 15.00 μm/h, and 10.75 μm/h in PDMS-DISH, PDMS-GLASS, PDMS-PDMS, and PMMA-PMMA, respectively. This study turns open up opportunities for new biochips in prospective applications of wound healing and antiscarring expected in drug screening and the related fields.
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