Britton Chance Center for Biomedical Photonics at Wuhan National Laboratory for Optoelectronics-Hubei Bioinformatics, Systems Biology Theme, Department of Biomedical Engineering, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, 430074, China.
Anal Bioanal Chem. 2013 Jan;405(1):307-14. doi: 10.1007/s00216-012-6447-z. Epub 2012 Oct 6.
Intercellular Ca(2+) waves are propagation of Ca(2+) transients among cells that could be initiated by chemical stimulation. Current methods for analyzing intercellular Ca(2+) waves are difficult to realize localized chemical stimulations upon the target cell without interfering with adjacent contacting cells. In this paper, a simple and flexible microfluidic method was developed for investigating the intercellular communication of Ca(2+) signals. A cross-patterned microfluidic chip was designed and fabricated with polydimethylsiloxane as the structural material. Localized chemical stimulation was achieved by a new strategy based on hydrodynamic gating technique. Clusters of target cells were seeded at the location within 300 μm downstream of the intersection of the cross-shaped microchannel. Confined lateral molecular diffusion largely minimized the interference from diffusion-induced stimulation of adjacent cells. Localized stimulation of the target cell with adenosine 5'-triphosphate successfully induced the propagation of intercellular Ca(2+) waves among a population of adjacent contacting cells. Further inhibition studies verified that the propagation of calcium signals among NIH-3 T3 cells was dependent on direct cytosolic transfer via gap junctions. The developed microfluidic method provides a versatile platform for investigating the dynamics of intercellular communications.
细胞间 Ca(2+)波是细胞间 Ca(2+)瞬变的传播,它可以通过化学刺激引发。目前分析细胞间 Ca(2+)波的方法很难在不干扰相邻接触细胞的情况下,对靶细胞进行局部化学刺激。在本文中,开发了一种简单灵活的微流控方法来研究 Ca(2+)信号的细胞间通讯。使用聚二甲基硅氧烷作为结构材料设计并制造了具有交叉图案的微流控芯片。通过基于流体力学门控技术的新策略实现了局部化学刺激。靶细胞簇被种植在交叉微通道交汇处下游 300 μm 范围内的位置。受限的侧向分子扩散极大地减少了相邻细胞扩散诱导刺激的干扰。用三磷酸腺苷对靶细胞进行局部刺激成功地诱导了一群相邻接触细胞之间的细胞间 Ca(2+)波的传播。进一步的抑制研究验证了 NIH-3T3 细胞之间钙信号的传播依赖于通过间隙连接的细胞质直接转移。所开发的微流控方法为研究细胞间通讯的动力学提供了一个通用平台。