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Syringe-injectable Mesh Electronics for Stable Chronic Rodent Electrophysiology

Implantable brain electrophysiology probes are valuable tools in neuroscience due to their ability to record neural activity with high spatiotemporal resolution from shallow and deep brain regions. Their use has been hindered, however, by mechanical and structural mismatches between the probes and b...

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Autores principales: Schuhmann, Thomas G., Zhou, Tao, Hong, Guosong, Lee, Jung Min, Fu, Tian-Ming, Park, Hong-Gyu, Lieber, Charles M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126522/
https://www.ncbi.nlm.nih.gov/pubmed/30080192
http://dx.doi.org/10.3791/58003
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author Schuhmann, Thomas G.
Zhou, Tao
Hong, Guosong
Lee, Jung Min
Fu, Tian-Ming
Park, Hong-Gyu
Lieber, Charles M.
author_facet Schuhmann, Thomas G.
Zhou, Tao
Hong, Guosong
Lee, Jung Min
Fu, Tian-Ming
Park, Hong-Gyu
Lieber, Charles M.
author_sort Schuhmann, Thomas G.
collection PubMed
description Implantable brain electrophysiology probes are valuable tools in neuroscience due to their ability to record neural activity with high spatiotemporal resolution from shallow and deep brain regions. Their use has been hindered, however, by mechanical and structural mismatches between the probes and brain tissue that commonly lead to micromotion and gliosis with resulting signal instability in chronic recording experiments. In contrast, following the implantation of ultraflexible mesh electronics via syringe injection, the mesh probes form a seamless, gliosis-free interface with the surrounding brain tissue that enables stable tracking of individual neurons on at least a year timescale. This protocol details the key steps in a typical mouse neural recording experiment using syringe-injectable mesh electronics, including the fabrication of mesh electronics in a standard photolithography-based process possible at many universities, loading mesh electronics into standard capillary needles, stereotaxic injection in vivo, connection of the mesh input/output to standard instrumentation interfaces, restrained or freely moving recording sessions, and histological sectioning of brain tissue containing mesh electronics. Representative neural recordings and histology data are presented. Investigators familiar with this protocol will have the knowledge necessary to incorporate mesh electronics into their own experiments and take advantage of the unique opportunities afforded by long-term stable neural interfacing, such as studies of aging processes, brain development, and the pathogenesis of brain disease.
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spelling pubmed-61265222018-09-19 Syringe-injectable Mesh Electronics for Stable Chronic Rodent Electrophysiology Schuhmann, Thomas G. Zhou, Tao Hong, Guosong Lee, Jung Min Fu, Tian-Ming Park, Hong-Gyu Lieber, Charles M. J Vis Exp Bioengineering Implantable brain electrophysiology probes are valuable tools in neuroscience due to their ability to record neural activity with high spatiotemporal resolution from shallow and deep brain regions. Their use has been hindered, however, by mechanical and structural mismatches between the probes and brain tissue that commonly lead to micromotion and gliosis with resulting signal instability in chronic recording experiments. In contrast, following the implantation of ultraflexible mesh electronics via syringe injection, the mesh probes form a seamless, gliosis-free interface with the surrounding brain tissue that enables stable tracking of individual neurons on at least a year timescale. This protocol details the key steps in a typical mouse neural recording experiment using syringe-injectable mesh electronics, including the fabrication of mesh electronics in a standard photolithography-based process possible at many universities, loading mesh electronics into standard capillary needles, stereotaxic injection in vivo, connection of the mesh input/output to standard instrumentation interfaces, restrained or freely moving recording sessions, and histological sectioning of brain tissue containing mesh electronics. Representative neural recordings and histology data are presented. Investigators familiar with this protocol will have the knowledge necessary to incorporate mesh electronics into their own experiments and take advantage of the unique opportunities afforded by long-term stable neural interfacing, such as studies of aging processes, brain development, and the pathogenesis of brain disease. MyJove Corporation 2018-07-21 /pmc/articles/PMC6126522/ /pubmed/30080192 http://dx.doi.org/10.3791/58003 Text en Copyright © 2018, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Bioengineering
Schuhmann, Thomas G.
Zhou, Tao
Hong, Guosong
Lee, Jung Min
Fu, Tian-Ming
Park, Hong-Gyu
Lieber, Charles M.
Syringe-injectable Mesh Electronics for Stable Chronic Rodent Electrophysiology
title Syringe-injectable Mesh Electronics for Stable Chronic Rodent Electrophysiology
title_full Syringe-injectable Mesh Electronics for Stable Chronic Rodent Electrophysiology
title_fullStr Syringe-injectable Mesh Electronics for Stable Chronic Rodent Electrophysiology
title_full_unstemmed Syringe-injectable Mesh Electronics for Stable Chronic Rodent Electrophysiology
title_short Syringe-injectable Mesh Electronics for Stable Chronic Rodent Electrophysiology
title_sort syringe-injectable mesh electronics for stable chronic rodent electrophysiology
topic Bioengineering
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6126522/
https://www.ncbi.nlm.nih.gov/pubmed/30080192
http://dx.doi.org/10.3791/58003
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