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Ultraflexible nanoelectronic probes form reliable, glial scar–free neural integration
Implanted brain electrodes construct the only means to electrically interface with individual neurons in vivo, but their recording efficacy and biocompatibility pose limitations on scientific and clinical applications. We showed that nanoelectronic thread (NET) electrodes with subcellular dimensions...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5310823/ https://www.ncbi.nlm.nih.gov/pubmed/28246640 http://dx.doi.org/10.1126/sciadv.1601966 |
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author | Luan, Lan Wei, Xiaoling Zhao, Zhengtuo Siegel, Jennifer J. Potnis, Ojas Tuppen, Catherine A Lin, Shengqing Kazmi, Shams Fowler, Robert A. Holloway, Stewart Dunn, Andrew K. Chitwood, Raymond A. Xie, Chong |
author_facet | Luan, Lan Wei, Xiaoling Zhao, Zhengtuo Siegel, Jennifer J. Potnis, Ojas Tuppen, Catherine A Lin, Shengqing Kazmi, Shams Fowler, Robert A. Holloway, Stewart Dunn, Andrew K. Chitwood, Raymond A. Xie, Chong |
author_sort | Luan, Lan |
collection | PubMed |
description | Implanted brain electrodes construct the only means to electrically interface with individual neurons in vivo, but their recording efficacy and biocompatibility pose limitations on scientific and clinical applications. We showed that nanoelectronic thread (NET) electrodes with subcellular dimensions, ultraflexibility, and cellular surgical footprints form reliable, glial scar–free neural integration. We demonstrated that NET electrodes reliably detected and tracked individual units for months; their impedance, noise level, single-unit recording yield, and the signal amplitude remained stable during long-term implantation. In vivo two-photon imaging and postmortem histological analysis revealed seamless, subcellular integration of NET probes with the local cellular and vasculature networks, featuring fully recovered capillaries with an intact blood-brain barrier and complete absence of chronic neuronal degradation and glial scar. |
format | Online Article Text |
id | pubmed-5310823 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-53108232017-02-28 Ultraflexible nanoelectronic probes form reliable, glial scar–free neural integration Luan, Lan Wei, Xiaoling Zhao, Zhengtuo Siegel, Jennifer J. Potnis, Ojas Tuppen, Catherine A Lin, Shengqing Kazmi, Shams Fowler, Robert A. Holloway, Stewart Dunn, Andrew K. Chitwood, Raymond A. Xie, Chong Sci Adv Research Articles Implanted brain electrodes construct the only means to electrically interface with individual neurons in vivo, but their recording efficacy and biocompatibility pose limitations on scientific and clinical applications. We showed that nanoelectronic thread (NET) electrodes with subcellular dimensions, ultraflexibility, and cellular surgical footprints form reliable, glial scar–free neural integration. We demonstrated that NET electrodes reliably detected and tracked individual units for months; their impedance, noise level, single-unit recording yield, and the signal amplitude remained stable during long-term implantation. In vivo two-photon imaging and postmortem histological analysis revealed seamless, subcellular integration of NET probes with the local cellular and vasculature networks, featuring fully recovered capillaries with an intact blood-brain barrier and complete absence of chronic neuronal degradation and glial scar. American Association for the Advancement of Science 2017-02-15 /pmc/articles/PMC5310823/ /pubmed/28246640 http://dx.doi.org/10.1126/sciadv.1601966 Text en Copyright © 2017, The Authors http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Luan, Lan Wei, Xiaoling Zhao, Zhengtuo Siegel, Jennifer J. Potnis, Ojas Tuppen, Catherine A Lin, Shengqing Kazmi, Shams Fowler, Robert A. Holloway, Stewart Dunn, Andrew K. Chitwood, Raymond A. Xie, Chong Ultraflexible nanoelectronic probes form reliable, glial scar–free neural integration |
title | Ultraflexible nanoelectronic probes form reliable, glial scar–free neural integration |
title_full | Ultraflexible nanoelectronic probes form reliable, glial scar–free neural integration |
title_fullStr | Ultraflexible nanoelectronic probes form reliable, glial scar–free neural integration |
title_full_unstemmed | Ultraflexible nanoelectronic probes form reliable, glial scar–free neural integration |
title_short | Ultraflexible nanoelectronic probes form reliable, glial scar–free neural integration |
title_sort | ultraflexible nanoelectronic probes form reliable, glial scar–free neural integration |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5310823/ https://www.ncbi.nlm.nih.gov/pubmed/28246640 http://dx.doi.org/10.1126/sciadv.1601966 |
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