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首页> 外文期刊>Microsystems & Nanoengineering >Large-scale microfluidic gradient arrays reveal axon guidance behaviors in hippocampal neurons
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Large-scale microfluidic gradient arrays reveal axon guidance behaviors in hippocampal neurons

机译:大规模的微流控梯度阵列揭示海马神经元的轴突指导行为。

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摘要

A large-scale microfluidic array has uncovered how chemical concentration gradients can manipulate delicate mammalian neurons. Although researchers agree that diffusible proteins direct nerve cells to grow and migrate using narrow projections known as axons, observing these effects with conventional micropipette experiments is difficult and time-consuming. To simplify such measurements, a team led by Nirveek Bhattacharjee and Albert Folch at the University of Washington, United States, fabricated a polydimethylsiloxane array of 1,024 microscale reservoirs containing molded microchannels that introduce fluids at controlled rates and create identical concentration gradients of a signaling protein in each reservoir. After seeding the chambers with single hippocampal neurons, the team tracked the growth dynamics of the cells using time-lapse microscopy. High-throughput analysis of hundreds of such neurons revealed that axons grow towards the source under high concentrations of a signaling protein but turn away from it at lower concentrations.
机译:大规模的微流控阵列已经揭示了化学浓度梯度可以如何操纵精致的哺乳动物神经元。尽管研究人员一致认为,可扩散的蛋白质会通过称为轴突的狭窄投影引导神经细胞生长和迁移,但使用常规微量移液器实验观察这些效果既困难又费时。为简化此类测量,美国华盛顿大学的Nirveek Bhattacharjee和Albert Folch领导的团队制造了一个1,024个微尺度储层的聚二甲基硅氧烷阵列,其中包含模制微通道,这些微通道以受控的速率引入流体,并在体内形成相同的信号传导蛋白浓度梯度。每个水库。在将单个海马神经元接种到室内后,研究小组使用延时显微镜观察了细胞的生长动态。对数百个此类神经元的高通量分析显示,轴突在高浓度信号蛋白的作用下向着源头生长,而在较低浓度时则远离轴突。

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