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An in vitro method to manipulate the direction and functional strength between neural populations

We report the design and application of a Micro Electro Mechanical Systems (MEMs) device that permits investigators to create arbitrary network topologies. With this device investigators can manipulate the degree of functional connectivity among distinct neural populations by systematically altering...

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Autores principales: Pan, Liangbin, Alagapan, Sankaraleengam, Franca, Eric, Leondopulos, Stathis S., DeMarse, Thomas B., Brewer, Gregory J., Wheeler, Bruce C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4500931/
https://www.ncbi.nlm.nih.gov/pubmed/26236198
http://dx.doi.org/10.3389/fncir.2015.00032
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author Pan, Liangbin
Alagapan, Sankaraleengam
Franca, Eric
Leondopulos, Stathis S.
DeMarse, Thomas B.
Brewer, Gregory J.
Wheeler, Bruce C.
author_facet Pan, Liangbin
Alagapan, Sankaraleengam
Franca, Eric
Leondopulos, Stathis S.
DeMarse, Thomas B.
Brewer, Gregory J.
Wheeler, Bruce C.
author_sort Pan, Liangbin
collection PubMed
description We report the design and application of a Micro Electro Mechanical Systems (MEMs) device that permits investigators to create arbitrary network topologies. With this device investigators can manipulate the degree of functional connectivity among distinct neural populations by systematically altering their geometric connectivity in vitro. Each polydimethylsilxane (PDMS) device was cast from molds and consisted of two wells each containing a small neural population of dissociated rat cortical neurons. Wells were separated by a series of parallel micrometer scale tunnels that permitted passage of axonal processes but not somata; with the device placed over an 8 × 8 microelectrode array, action potentials from somata in wells and axons in microtunnels can be recorded and stimulated. In our earlier report we showed that a one week delay in plating of neurons from one well to the other led to a filling and blocking of the microtunnels by axons from the older well resulting in strong directionality (older to younger) of both axon action potentials in tunnels and longer duration and more slowly propagating bursts of action potentials between wells. Here we show that changing the number of tunnels, and hence the number of axons, connecting the two wells leads to changes in connectivity and propagation of bursting activity. More specifically, the greater the number of tunnels the stronger the connectivity, the greater the probability of bursting propagating between wells, and shorter peak-to-peak delays between bursts and time to first spike measured in the opposing well. We estimate that a minimum of 100 axons are needed to reliably initiate a burst in the opposing well. This device provides a tool for researchers interested in understanding network dynamics who will profit from having the ability to design both the degree and directionality connectivity among multiple small neural populations.
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spelling pubmed-45009312015-07-31 An in vitro method to manipulate the direction and functional strength between neural populations Pan, Liangbin Alagapan, Sankaraleengam Franca, Eric Leondopulos, Stathis S. DeMarse, Thomas B. Brewer, Gregory J. Wheeler, Bruce C. Front Neural Circuits Neuroscience We report the design and application of a Micro Electro Mechanical Systems (MEMs) device that permits investigators to create arbitrary network topologies. With this device investigators can manipulate the degree of functional connectivity among distinct neural populations by systematically altering their geometric connectivity in vitro. Each polydimethylsilxane (PDMS) device was cast from molds and consisted of two wells each containing a small neural population of dissociated rat cortical neurons. Wells were separated by a series of parallel micrometer scale tunnels that permitted passage of axonal processes but not somata; with the device placed over an 8 × 8 microelectrode array, action potentials from somata in wells and axons in microtunnels can be recorded and stimulated. In our earlier report we showed that a one week delay in plating of neurons from one well to the other led to a filling and blocking of the microtunnels by axons from the older well resulting in strong directionality (older to younger) of both axon action potentials in tunnels and longer duration and more slowly propagating bursts of action potentials between wells. Here we show that changing the number of tunnels, and hence the number of axons, connecting the two wells leads to changes in connectivity and propagation of bursting activity. More specifically, the greater the number of tunnels the stronger the connectivity, the greater the probability of bursting propagating between wells, and shorter peak-to-peak delays between bursts and time to first spike measured in the opposing well. We estimate that a minimum of 100 axons are needed to reliably initiate a burst in the opposing well. This device provides a tool for researchers interested in understanding network dynamics who will profit from having the ability to design both the degree and directionality connectivity among multiple small neural populations. Frontiers Media S.A. 2015-07-14 /pmc/articles/PMC4500931/ /pubmed/26236198 http://dx.doi.org/10.3389/fncir.2015.00032 Text en Copyright © 2015 Pan, Alagapan, Franca, Leondopulos, DeMarse, Brewer and Wheeler. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Pan, Liangbin
Alagapan, Sankaraleengam
Franca, Eric
Leondopulos, Stathis S.
DeMarse, Thomas B.
Brewer, Gregory J.
Wheeler, Bruce C.
An in vitro method to manipulate the direction and functional strength between neural populations
title An in vitro method to manipulate the direction and functional strength between neural populations
title_full An in vitro method to manipulate the direction and functional strength between neural populations
title_fullStr An in vitro method to manipulate the direction and functional strength between neural populations
title_full_unstemmed An in vitro method to manipulate the direction and functional strength between neural populations
title_short An in vitro method to manipulate the direction and functional strength between neural populations
title_sort in vitro method to manipulate the direction and functional strength between neural populations
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4500931/
https://www.ncbi.nlm.nih.gov/pubmed/26236198
http://dx.doi.org/10.3389/fncir.2015.00032
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