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Narrow microtunnel technology for the isolation and precise identification of axonal communication among distinct hippocampal subregion networks
Communication between different sub regions of the hippocampus is fundamental to learning and memory. However accurate knowledge about information transfer between sub regions from access to the activity in individual axons is lacking. MEMS devices with microtunnels connecting two sub networks have...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5426613/ https://www.ncbi.nlm.nih.gov/pubmed/28493886 http://dx.doi.org/10.1371/journal.pone.0176868 |
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author | Narula, Udit Ruiz, Andres McQuaide, McKinley DeMarse, Thomas B. Wheeler, Bruce C. Brewer, Gregory J. |
author_facet | Narula, Udit Ruiz, Andres McQuaide, McKinley DeMarse, Thomas B. Wheeler, Bruce C. Brewer, Gregory J. |
author_sort | Narula, Udit |
collection | PubMed |
description | Communication between different sub regions of the hippocampus is fundamental to learning and memory. However accurate knowledge about information transfer between sub regions from access to the activity in individual axons is lacking. MEMS devices with microtunnels connecting two sub networks have begun to approach this problem but the commonly used 10 μm wide tunnels frequently measure signals from multiple axons. To reduce this complexity, we compared polydimethylsiloxane (PDMS) microtunnel devices each with a separate tunnel width of 2.5, 5 or 10 μm bridging two wells aligned over a multi electrode array (MEA). Primary rat neurons were grown in the chambers with neurons from the dentate gyrus on one side and hippocampal CA3 on the other. After 2–3 weeks of culture, spontaneous activity in the axons inside the tunnels was recorded. We report electrophysiological, exploratory data analysis for feature clustering and visual evidence to support the expectation that 2.5 μm wide tunnels have fewer axons per tunnel and therefore more clearly delineated signals than 10 or 5 μm wide tunnels. Several measures indicated that fewer axons per electrode enabled more accurate detection of spikes. A clustering analysis comparing the variations of spike height and width for different tunnel widths revealed tighter clusters representing unique spikes with less height and width variation when measured in narrow tunnels. Wider tunnels tended toward more diffuse clusters from a continuum of spike heights and widths. Standard deviations for multiple cluster measures, such as Average Dissimilarity, Silhouette Value (S) and Separation Factor (average dissimilarity/S value), support a conclusion that 2.5 μm wide tunnels containing fewer axons enable more precise determination of individual action potential peaks, their propagation direction, timing, and information transfer between sub networks. |
format | Online Article Text |
id | pubmed-5426613 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54266132017-05-25 Narrow microtunnel technology for the isolation and precise identification of axonal communication among distinct hippocampal subregion networks Narula, Udit Ruiz, Andres McQuaide, McKinley DeMarse, Thomas B. Wheeler, Bruce C. Brewer, Gregory J. PLoS One Research Article Communication between different sub regions of the hippocampus is fundamental to learning and memory. However accurate knowledge about information transfer between sub regions from access to the activity in individual axons is lacking. MEMS devices with microtunnels connecting two sub networks have begun to approach this problem but the commonly used 10 μm wide tunnels frequently measure signals from multiple axons. To reduce this complexity, we compared polydimethylsiloxane (PDMS) microtunnel devices each with a separate tunnel width of 2.5, 5 or 10 μm bridging two wells aligned over a multi electrode array (MEA). Primary rat neurons were grown in the chambers with neurons from the dentate gyrus on one side and hippocampal CA3 on the other. After 2–3 weeks of culture, spontaneous activity in the axons inside the tunnels was recorded. We report electrophysiological, exploratory data analysis for feature clustering and visual evidence to support the expectation that 2.5 μm wide tunnels have fewer axons per tunnel and therefore more clearly delineated signals than 10 or 5 μm wide tunnels. Several measures indicated that fewer axons per electrode enabled more accurate detection of spikes. A clustering analysis comparing the variations of spike height and width for different tunnel widths revealed tighter clusters representing unique spikes with less height and width variation when measured in narrow tunnels. Wider tunnels tended toward more diffuse clusters from a continuum of spike heights and widths. Standard deviations for multiple cluster measures, such as Average Dissimilarity, Silhouette Value (S) and Separation Factor (average dissimilarity/S value), support a conclusion that 2.5 μm wide tunnels containing fewer axons enable more precise determination of individual action potential peaks, their propagation direction, timing, and information transfer between sub networks. Public Library of Science 2017-05-11 /pmc/articles/PMC5426613/ /pubmed/28493886 http://dx.doi.org/10.1371/journal.pone.0176868 Text en © 2017 Narula et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Narula, Udit Ruiz, Andres McQuaide, McKinley DeMarse, Thomas B. Wheeler, Bruce C. Brewer, Gregory J. Narrow microtunnel technology for the isolation and precise identification of axonal communication among distinct hippocampal subregion networks |
title | Narrow microtunnel technology for the isolation and precise identification of axonal communication among distinct hippocampal subregion networks |
title_full | Narrow microtunnel technology for the isolation and precise identification of axonal communication among distinct hippocampal subregion networks |
title_fullStr | Narrow microtunnel technology for the isolation and precise identification of axonal communication among distinct hippocampal subregion networks |
title_full_unstemmed | Narrow microtunnel technology for the isolation and precise identification of axonal communication among distinct hippocampal subregion networks |
title_short | Narrow microtunnel technology for the isolation and precise identification of axonal communication among distinct hippocampal subregion networks |
title_sort | narrow microtunnel technology for the isolation and precise identification of axonal communication among distinct hippocampal subregion networks |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5426613/ https://www.ncbi.nlm.nih.gov/pubmed/28493886 http://dx.doi.org/10.1371/journal.pone.0176868 |
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