Literature DB >> 16508072

Microfluidic chambers for cell migration and neuroscience research.

Anne M Taylor1, Seog Woo Rhee, Noo Li Jeon.   

Abstract

This chapter describes the fabrication and use microfluidic chambers for cell migration and neuroscience research. Both microfluidic chambers are made using soft lithography and replica molding. The main advantages of using soft lithography to create microfluidic chambers are reproducibility, ease of use, and straightforward fabrication procedures. The devices can be fabricated in biology and chemistry laboratories with minimal access to clean-room facilities. First, a microfluidic chemotaxis chamber, which has been used in investigating chemotaxis of neutrophils, human breast cancer cells, and other cell types, is described. Precise and stable gradients of chemoattractants with arbitrary shapes can be generated for different applications. Second, a multicompartment culture chamber that can fluidically isolate neuronal processes from cell bodies is described. The design of this chamber is such that only neurites grow through a series of microgrooves embedded in a physical barrier. Both devices are compatible with phase, differential interference contrast, and fluorescence microscopy.

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Mesh:

Year:  2006        PMID: 16508072     DOI: 10.1385/1-59259-997-4:167

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  25 in total

1.  A novel method for producing mono-biotinylated, biologically active neurotrophic factors: an essential reagent for single molecule study of axonal transport.

Authors:  Kijung Sung; Michael T Maloney; Jingkun Yang; Chengbiao Wu
Journal:  J Neurosci Methods       Date:  2011-07-02       Impact factor: 2.390

2.  Multilayer PDMS microfluidic chamber for controlling brain slice microenvironment.

Authors:  A J Blake; T M Pearce; N S Rao; S M Johnson; J C Williams
Journal:  Lab Chip       Date:  2007-05-24       Impact factor: 6.799

3.  Biomedical Technologies for in vitro Screening and Controlled Delivery of Neuroactive Compounds.

Authors:  John P Frampton; Michael L Shuler; William Shain; Matthew R Hynd
Journal:  Cent Nerv Syst Agents Med Chem       Date:  2008

4.  Disruption of the coxsackievirus and adenovirus receptor-homodimeric interaction triggers lipid microdomain- and dynamin-dependent endocytosis and lysosomal targeting.

Authors:  Sara Salinas; Charleine Zussy; Fabien Loustalot; Daniel Henaff; Guillermo Menendez; Penny E Morton; Maddy Parsons; Giampietro Schiavo; Eric J Kremer
Journal:  J Biol Chem       Date:  2013-11-22       Impact factor: 5.157

5.  Passive microfluidic chamber for long-term imaging of axon guidance in response to soluble gradients.

Authors:  A M Taylor; S Menon; S L Gupton
Journal:  Lab Chip       Date:  2015-05-22       Impact factor: 6.799

6.  A Customizable Chamber for Measuring Cell Migration.

Authors:  Aniqa N Chowdhury; Huu Tri Vo; Sharon Olang; Elliott Mappus; Brian Peterson; Nora Hlavac; Tyler Harvey; Delphine Dean
Journal:  J Vis Exp       Date:  2017-03-12       Impact factor: 1.355

7.  Single-molecule imaging of NGF axonal transport in microfluidic devices.

Authors:  Kai Zhang; Yasuko Osakada; Marija Vrljic; Liang Chen; Harsha V Mudrakola; Bianxiao Cui
Journal:  Lab Chip       Date:  2010-07-09       Impact factor: 6.799

8.  A novel electro-chemotactic approach to impact the directional migration of transplantable retinal progenitor cells.

Authors:  Shawn Mishra; Juan S Peña; Stephen Redenti; Maribel Vazquez
Journal:  Exp Eye Res       Date:  2019-06-08       Impact factor: 3.467

9.  Hypoxic injury of isolated axons is independent of ionotropic glutamate receptors.

Authors:  Suzanne M Underhill; Mark P Goldberg
Journal:  Neurobiol Dis       Date:  2006-10-27       Impact factor: 5.996

10.  Production of compartmented cultures of rat sympathetic neurons.

Authors:  Robert B Campenot; Karen Lund; Sue-Ann Mok
Journal:  Nat Protoc       Date:  2009       Impact factor: 13.491

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