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A neuron-benign microfluidic gradient generator for studying the response of mammalian neurons towards axon guidance factors

机译:一种神经元良性微流梯度发生器,用于研究哺乳动物神经元对轴突指导因子的反应

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摘要

Investigation of biochemical cues in isolation or in combinations in cell culture systems is crucial for unraveling the mechanisms that govern neural development and repair. The most widely used experimental paradigms that elicit axon guidance in vitro utilize as the source of the gradient a pulsatile pipette, transfected cells, or a loaded gel, producing time-varying gradients of poor reproducibility which are not well suited for studying slow-growing mammalian cells. Although microfluidic device design have allowed for generating stable, complex gradients of diffusible molecules, the flow-induced shear forces in a microchannel has made it impossible to maintain viable mammalian neuronal cultures for sufficiently long times. In this paper, we describe axonal responses of mouse cortical neurons in a “neuron-benign” gradient-generator device based on an open chamber that can establish highly stable gradients of diffusible molecules for at least 6 h with negligible shear stress, and also allows the neurons to thrive for at least 2 weeks. Except for the period when the gradient is on, the cells in the gradient are under the same conditions as the cells on the control surfaces, which ensure a consistent set of micro-environmental variables. The gradient stability and uniformity over the cell culture surface achieved by the device, together with our software platform for acquiring, post-processing and quantitatively analyzing the large number of images allowed us to extract valuable information even from small datasets. We report a directed response of primary mammalian neurons (from E14 embryonic mice cortex) to a diffusible gradient of netrin in vitro. We infer from our studies that a large majority (73%) of the neurons that extend axons during the gradient application grow towards the netrin source, and our data analysis also indicates that netrin acts as a growth factor for this same population of neurons.
机译:在细胞培养系统中分离或组合研究生化线索对于阐明控制神经发育和修复的机制至关重要。引起轴突引导的最广泛使用的实验范式利用搏动吸管,转染的细胞或上样的凝胶作为梯度的来源,产生了重现性差的随时间变化的梯度,不适用于研究生长缓慢的哺乳动物细胞。尽管微流体装置的设计允许产生稳定的,复杂的可扩散分子梯度,但是在微通道中由流动引起的剪切力使得不可能将存活的哺乳动物神经元培养物维持足够长的时间。在本文中,我们描述了基于开放腔室的“神经元良性”梯度发生器中的小鼠皮质神经元的轴突反应,该开放腔室可在至少6 h的剪切应力可忽略的情况下建立可扩散分子的高度稳定梯度,并且还允许神经元至少存活2周。除了打开渐变的时间段外,渐变中的单元格与控制表面上的单元格处于相同条件下,这确保了一组一致的微环境变量。该设备在细胞培养表面上实现的梯度稳定性和均匀性,再加上我们用于获取,后处理和定量分析大量图像的软件平台,使我们甚至可以从较小的数据集中提取有价值的信息。我们报告了主要的哺乳动物神经元(从E14胚胎小鼠皮层)定向反应的netrin在体外的可扩散梯度。从我们的研究中可以推断出,在梯度施加过程中,大多数轴突中延伸轴突的神经元(73%)朝着netrin源生长,并且我们的数据分析还表明netrin充当了同一神经元群体的生长因子。

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  • 来源
    《Integrative Biology》 |2010年第12期|p.669-679|共11页
  • 作者单位

    1. Department of Bioengineering,University of Washington, William H. Foege Building, Rm. N430-N, 3720 15th Ave NE, Campus Box 355061, Seattle, USA;

    1. Department of Bioengineering,University of Washington, William H. Foege Building, Rm. N430-N, 3720 15th Ave NE, Campus Box 355061, Seattle, USA;

    1. Department of Bioengineering,University of Washington, William H. Foege Building, Rm. N430-N, 3720 15th Ave NE, Campus Box 355061, Seattle, USA;

    1. Department of Bioengineering,University of Washington, William H. Foege Building, Rm. N430-N, 3720 15th Ave NE, Campus Box 355061, Seattle, USA;

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