Literature DB >> 18989432

Fabrication of a microfluidic device for the compartmentalization of neuron soma and axons.

Joseph Harris1, Hyuna Lee, Behrad Vahidi, Christina Tu, David Cribbs, Noo Li Jeon, Carl Cotman.   

Abstract

In this video, we demonstrate the technique of soft lithography with polydimethyl siloxane (PDMS) which we use to fabricate a microfluidic device for culturing neurons. Previously, a silicon wafer was patterned with the design for the neuron microfluidic device using SU-8 and photolithography to create a master mold, or what we simply refer to as a "master". Next, we pour the silicon polymer PDMS on top of the master which is then cured by heating the PDMS to 80 degrees C for 1 hour. The PDMS forms a negative mold of the device. The PDMS is then carefully cut and lifted away from the master. Holes are punched where the reservoirs will be and the excess PDMS trimmed away from the device. Nitrogen is used to blow away any excess debris from the device. At this point the devices are now ready for use and can either bonded to corning No. 1 cover glass with a plasma sterilizer/cleaner or can be reversibly bound to the cover glass by simply placing the device on top of the cover glass. The reversible bonding of the device to glass is covered in a separate video and requires first that the device be sterilized either with 70% ethanol or by autoclaving. Plasma treating sterilizes the devices so no further treatment is necessary. It is, however, important, when plasma-treating the devices, to add liquid to the devices within 10 minutes of the plasma treatment while the surfaces are still hydrophilic. Waiting longer than 10 minutes to add liquid to the device makes it difficult for the liquid to enter the device. The neuron devices are typically plasma-bound to cover glass and 0.5 mg/ml poly-L-lysine (PLL) in pH 8.5 borate buffer is immediately added to the device. After a minimum of 3 hours incubating with PLL, the devices are washed with dH2O water a minimum of 3 times with at least 15 minutes between each wash. Next, the water is removed and fresh media is added to the device. At this point the device is ready for use. It is important to remember at this point to never remove all the media from the device. Always leave media in the main channel.

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Mesh:

Year:  2007        PMID: 18989432      PMCID: PMC2565860          DOI: 10.3791/261

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  2 in total

1.  A microfluidic culture platform for CNS axonal injury, regeneration and transport.

Authors:  Anne M Taylor; Mathew Blurton-Jones; Seog Woo Rhee; David H Cribbs; Carl W Cotman; Noo Li Jeon
Journal:  Nat Methods       Date:  2005-08       Impact factor: 28.547

2.  Microfluidic culture platform for neuroscience research.

Authors:  Jeong Won Park; Behrad Vahidi; Anne M Taylor; Seog Woo Rhee; Noo Li Jeon
Journal:  Nat Protoc       Date:  2006       Impact factor: 13.491

  2 in total
  6 in total

1.  Characterizing the composition of molecular motors on moving axonal cargo using "cargo mapping" analysis.

Authors:  Sylvia Neumann; George E Campbell; Lukasz Szpankowski; Lawrence S B Goldstein; Sandra E Encalada
Journal:  J Vis Exp       Date:  2014-10-30       Impact factor: 1.355

2.  Picoinjection of microfluidic drops without metal electrodes.

Authors:  Brian O'Donovan; Tuan Tran; Adam Sciambi; Adam Abate
Journal:  J Vis Exp       Date:  2014-04-18       Impact factor: 1.355

3.  Single chain variable fragment antibodies block aggregation and toxicity induced by familial ALS-linked mutant forms of SOD1.

Authors:  Ghanashyam D Ghadge; John D Pavlovic; Sujatha P Koduvayur; Brian K Kay; Raymond P Roos
Journal:  Neurobiol Dis       Date:  2013-04-20       Impact factor: 5.996

4.  Anterograde monosynaptic transneuronal tracers derived from herpes simplex virus 1 strain H129.

Authors:  Wen-Bo Zeng; Hai-Fei Jiang; Ya-Dong Gang; Yi-Ge Song; Zhang-Zhou Shen; Hong Yang; Xiao Dong; Yong-Lu Tian; Rong-Jun Ni; Yaping Liu; Na Tang; Xinyan Li; Xuan Jiang; Ding Gao; Michelle Androulakis; Xiao-Bin He; Hui-Min Xia; Ying-Zi Ming; Youming Lu; Jiang-Ning Zhou; Chen Zhang; Xue-Shan Xia; Yousheng Shu; Shao-Qun Zeng; Fuqiang Xu; Fei Zhao; Min-Hua Luo
Journal:  Mol Neurodegener       Date:  2017-05-12       Impact factor: 14.195

5.  Retrograde interferon-gamma signaling induces major histocompatibility class I expression in human-induced pluripotent stem cell-derived neurons.

Authors:  Benjamin D S Clarkson; Misha S Patel; Reghann G LaFrance-Corey; Charles L Howe
Journal:  Ann Clin Transl Neurol       Date:  2017-12-21       Impact factor: 4.511

6.  Proteolytically released Lasso/teneurin-2 induces axonal attraction by interacting with latrophilin-1 on axonal growth cones.

Authors:  Nickolai V Vysokov; John-Paul Silva; Vera G Lelianova; Jason Suckling; John Cassidy; Jennifer K Blackburn; Natalia Yankova; Mustafa Ba Djamgoz; Serguei V Kozlov; Alexander G Tonevitsky; Yuri A Ushkaryov
Journal:  Elife       Date:  2018-11-20       Impact factor: 8.140

  6 in total

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