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Chemical Stimulation of Adherent Cells by Localized Application of Acetylcholine from a Microfluidic System
Chemical stimulation of cells is inherently cell type selective in contrast to electro-stimulation. The availability of a system for localized application of minute amounts of chemical stimulants could be useful for dose related response studies to test new compounds. It could also bring forward the...
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Formato: | Texto |
Lenguaje: | English |
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Frontiers Research Foundation
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2999818/ https://www.ncbi.nlm.nih.gov/pubmed/21151808 http://dx.doi.org/10.3389/fneng.2010.00113 |
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author | Zibek, Susanne Hagmeyer, Britta Stett, Alfred Stelzle, Martin |
author_facet | Zibek, Susanne Hagmeyer, Britta Stett, Alfred Stelzle, Martin |
author_sort | Zibek, Susanne |
collection | PubMed |
description | Chemical stimulation of cells is inherently cell type selective in contrast to electro-stimulation. The availability of a system for localized application of minute amounts of chemical stimulants could be useful for dose related response studies to test new compounds. It could also bring forward the development of a novel type of neuroprostheses. In an experimental setup microdroplets of an acetylcholine solution were ejected from a fluidic microsystem and applied to the bottom of a nanoporous membrane. The solution traveled through the pores to the top of the membrane on which TE671 cells were cultivated. Calcium imaging was used to visualize cellular response with temporal and spatial resolution. Experimental demonstration of chemical stimulation for both threshold gated stimulation as well as accumulated dose–response was achieved by either employing acetylcholine as chemical stimulant or applying calcein uptake, respectively. Numerical modeling and simulation of transport mechanisms involved were employed to gain a theoretical understanding of the influence of pore size, concentration of stimulant and droplet volume on the spatial-temporal distribution of stimulant and on the cellular response. Diffusion, pressure driven flow and evaporation effects were taken into account. Fast stimulation kinetic is achieved with pores of 0.82 μm diameter, whereas sustained substance delivery is obtained with nanoporous membranes. In all cases threshold concentrations ranging from 0.01 to 0.015 μM acetylcholine independent of pore size were determined. |
format | Text |
id | pubmed-2999818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-29998182010-12-10 Chemical Stimulation of Adherent Cells by Localized Application of Acetylcholine from a Microfluidic System Zibek, Susanne Hagmeyer, Britta Stett, Alfred Stelzle, Martin Front Neuroengineering Neuroscience Chemical stimulation of cells is inherently cell type selective in contrast to electro-stimulation. The availability of a system for localized application of minute amounts of chemical stimulants could be useful for dose related response studies to test new compounds. It could also bring forward the development of a novel type of neuroprostheses. In an experimental setup microdroplets of an acetylcholine solution were ejected from a fluidic microsystem and applied to the bottom of a nanoporous membrane. The solution traveled through the pores to the top of the membrane on which TE671 cells were cultivated. Calcium imaging was used to visualize cellular response with temporal and spatial resolution. Experimental demonstration of chemical stimulation for both threshold gated stimulation as well as accumulated dose–response was achieved by either employing acetylcholine as chemical stimulant or applying calcein uptake, respectively. Numerical modeling and simulation of transport mechanisms involved were employed to gain a theoretical understanding of the influence of pore size, concentration of stimulant and droplet volume on the spatial-temporal distribution of stimulant and on the cellular response. Diffusion, pressure driven flow and evaporation effects were taken into account. Fast stimulation kinetic is achieved with pores of 0.82 μm diameter, whereas sustained substance delivery is obtained with nanoporous membranes. In all cases threshold concentrations ranging from 0.01 to 0.015 μM acetylcholine independent of pore size were determined. Frontiers Research Foundation 2010-11-26 /pmc/articles/PMC2999818/ /pubmed/21151808 http://dx.doi.org/10.3389/fneng.2010.00113 Text en Copyright © 2010 Zibek, Hagmeyer, Stett and Stelzle. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited. |
spellingShingle | Neuroscience Zibek, Susanne Hagmeyer, Britta Stett, Alfred Stelzle, Martin Chemical Stimulation of Adherent Cells by Localized Application of Acetylcholine from a Microfluidic System |
title | Chemical Stimulation of Adherent Cells by Localized Application of Acetylcholine from a Microfluidic System |
title_full | Chemical Stimulation of Adherent Cells by Localized Application of Acetylcholine from a Microfluidic System |
title_fullStr | Chemical Stimulation of Adherent Cells by Localized Application of Acetylcholine from a Microfluidic System |
title_full_unstemmed | Chemical Stimulation of Adherent Cells by Localized Application of Acetylcholine from a Microfluidic System |
title_short | Chemical Stimulation of Adherent Cells by Localized Application of Acetylcholine from a Microfluidic System |
title_sort | chemical stimulation of adherent cells by localized application of acetylcholine from a microfluidic system |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2999818/ https://www.ncbi.nlm.nih.gov/pubmed/21151808 http://dx.doi.org/10.3389/fneng.2010.00113 |
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