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Reconfigurable microfluidics with integrated aptasensors for monitoring intercellular communication

机译:具有集成适体传感器的可重构微流体,用于监测细胞间通讯

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We report the development of a microsystem integrating anti-TNF-α aptasensors with vacuum-actuatable microfluidic devices that may be used to monitor intercellular communications. Actuatable chambers were used to expose to mitogen a group of ~600 cells while not stimulating another group of monocytes only 600 μm away. Co-localizing groups of cells with miniature 300 μm diameter aptamer-modified electrodes enabled monitoring of TNF-a release from each group independently. The microsystem allowed observation of the sequence of events that included 1) mitogenic activation of the first group of monocytes to produce TNF-α, 2) diffusion of TNF-α to the location of the second group of cells and 3) activation of the second group of cells resulting in the production of TNF-α by these cells. Thus, we were able to experimentally verify reciprocal paracrine crosstalk between the two groups of cells secreting the same signalling molecule. Given the prevalence of such cellular communications during injury, cancer or immune response and the dearth of available monitoring techniques, the microsystem described here is envisioned to have significant impact on cell biology.
机译:我们报告了将抗TNF-αaptasensors与可用于监视细胞间通讯的真空致动微流控设备集成在一起的微系统的发展。使用可启动腔室将一组约600个细胞暴露于有丝分裂原,而不刺激仅600μm处的另一组单核细胞。具有微型300μm直径适体修饰电极的细胞共定位组能够独立监测每组中TNF-α的释放。该微系统允许观察以下事件的顺序,包括:1)第一组单核细胞的促有丝分裂活化以产生TNF-α; 2)TNF-α扩散至第二组细胞的位置; 3)活化第二组细胞群导致这些细胞产生TNF-α。因此,我们能够通过实验验证分泌相同信号分子的两组细胞之间的相互旁分泌串扰。考虑到在损伤,癌症或免疫反应期间这种细胞通讯的普遍性以及缺乏可用的监测技术,可以预见此处描述的微系统将对细胞生物学产生重大影响。

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