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本文引用的文献

1
Short-term high-resolution imaging of developing hippocampal neurons in culture.培养中发育海马神经元的短期高分辨率成像。
Cold Spring Harb Protoc. 2012 Mar 1;2012(3):340-3. doi: 10.1101/pdb.prot068247.
2
Axon diodes for the reconstruction of oriented neuronal networks in microfluidic chambers.轴突二极管用于重建微流控室内定向神经元网络。
Lab Chip. 2011 Nov 7;11(21):3663-73. doi: 10.1039/c1lc20014c. Epub 2011 Sep 15.
3
Co-pathological connected primary neurons in a microfluidic device for Alzheimer studies.用于阿尔茨海默病研究的微流控装置中的共病理性连接原代神经元。
Biotechnol Bioeng. 2011 Sep;108(9):2241-5. doi: 10.1002/bit.23128. Epub 2011 Mar 21.
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Microfluidic Multicompartment Device for Neuroscience Research.用于神经科学研究的微流控多隔室装置
Langmuir. 2003 Mar 4;19(5):1551-1556. doi: 10.1021/la026417v.
5
Cell culture models in microfluidic systems.微流控系统中的细胞培养模型。
Annu Rev Anal Chem (Palo Alto Calif). 2008;1:423-49. doi: 10.1146/annurev.anchem.1.031207.113042.
6
Microfluidics: a new cosset for neurobiology.微流控技术:神经生物学的新宠儿。
Lab Chip. 2009 Mar 7;9(5):644-52. doi: 10.1039/b813495b. Epub 2008 Dec 18.
7
How mitochondria produce reactive oxygen species.线粒体如何产生活性氧物种。
Biochem J. 2009 Jan 1;417(1):1-13. doi: 10.1042/BJ20081386.
8
Sodium azide induced neuronal damage in vitro: evidence for non-apoptotic cell death.叠氮化钠在体外诱导神经元损伤:非凋亡性细胞死亡的证据。
Neurochem Res. 2009 May;34(5):909-16. doi: 10.1007/s11064-008-9852-0. Epub 2008 Oct 8.
9
Role of axonal transport in neurodegenerative diseases.轴突运输在神经退行性疾病中的作用。
Annu Rev Neurosci. 2008;31:151-73. doi: 10.1146/annurev.neuro.31.061307.090711.
10
A microfluidics-based turning assay reveals complex growth cone responses to integrated gradients of substrate-bound ECM molecules and diffusible guidance cues.一种基于微流控的转向试验揭示了生长锥对底物结合的细胞外基质分子和可扩散导向信号的整合梯度的复杂反应。
Lab Chip. 2008 Feb;8(2):227-37. doi: 10.1039/b713945d. Epub 2008 Jan 4.

原代大鼠海马神经元培养:细胞接种、定向生长和溶质输送的微流控装置的设计、分析和优化。

Culture of primary rat hippocampal neurons: design, analysis, and optimization of a microfluidic device for cell seeding, coherent growth, and solute delivery.

机构信息

Sibley School of Mechanical and Aerospace Engineering, Cornell University, Ithaca, NY, USA.

出版信息

Biomed Microdevices. 2013 Feb;15(1):97-108. doi: 10.1007/s10544-012-9691-2.

DOI:10.1007/s10544-012-9691-2
PMID:22965807
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3773545/
Abstract

We present the design, analysis, construction, and culture results of a microfluidic device for the segregation and chemical stimulation of primary rat hippocampal neurons. Our device is designed to achieve spatio-temporal solute delivery to discrete sections of neurons with mitigated mechanical stress. We implement a geometric guidance technique to direct axonal processes of the neurons into specific areas of the device to achieve solute segregation along routed cells. Using physicochemical modeling, we predict flows, concentration profiles, and mechanical stresses within pertiment sections of the device. We demonstrate cell viability and growth within the closed device over a period of 11 days. Additionally, our modeling methodology may be generalized and applied to other device geometries.

摘要

我们介绍了一种用于分离和化学刺激原代大鼠海马神经元的微流控装置的设计、分析、构建和培养结果。我们的装置旨在实现对神经元离散部分的时空溶质输送,同时减轻机械应力。我们采用几何引导技术将神经元的轴突过程引导到装置的特定区域,以实现沿路由细胞的溶质分离。通过物理化学建模,我们预测了装置中特定区域的流动、浓度分布和机械应力。我们证明了在 11 天的时间内,细胞在封闭装置内的存活和生长。此外,我们的建模方法可以推广并应用于其他装置几何形状。