Cargando…

Ultrastructural Analysis of Neuroimplant-Parenchyma Interfaces Uncover Remarkable Neuroregeneration Along-With Barriers That Limit the Implant Electrophysiological Functions

Despite increasing use of in vivo multielectrode array (MEA) implants for basic research and medical applications, the critical structural interfaces formed between the implants and the brain parenchyma, remain elusive. Prevailing view assumes that formation of multicellular inflammatory encapsulati...

Descripción completa

Detalles Bibliográficos
Autores principales: Sharon, Aviv, Shmoel, Nava, Erez, Hadas, Jankowski, Maciej M., Friedmann, Yael, Spira, Micha E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645653/
https://www.ncbi.nlm.nih.gov/pubmed/34880722
http://dx.doi.org/10.3389/fnins.2021.764448
_version_ 1784610354359173120
author Sharon, Aviv
Shmoel, Nava
Erez, Hadas
Jankowski, Maciej M.
Friedmann, Yael
Spira, Micha E.
author_facet Sharon, Aviv
Shmoel, Nava
Erez, Hadas
Jankowski, Maciej M.
Friedmann, Yael
Spira, Micha E.
author_sort Sharon, Aviv
collection PubMed
description Despite increasing use of in vivo multielectrode array (MEA) implants for basic research and medical applications, the critical structural interfaces formed between the implants and the brain parenchyma, remain elusive. Prevailing view assumes that formation of multicellular inflammatory encapsulating-scar around the implants [the foreign body response (FBR)] degrades the implant electrophysiological functions. Using gold mushroom shaped microelectrodes (gMμEs) based perforated polyimide MEA platforms (PPMPs) that in contrast to standard probes can be thin sectioned along with the interfacing parenchyma; we examined here for the first time the interfaces formed between brains parenchyma and implanted 3D vertical microelectrode platforms at the ultrastructural level. Our study demonstrates remarkable regenerative processes including neuritogenesis, axon myelination, synapse formation and capillaries regrowth in contact and around the implant. In parallel, we document that individual microglia adhere tightly and engulf the gMμEs. Modeling of the formed microglia-electrode junctions suggest that this configuration suffice to account for the low and deteriorating recording qualities of in vivo MEA implants. These observations help define the anticipated hurdles to adapting the advantageous 3D in vitro vertical-electrode technologies to in vivo settings, and suggest that improving the recording qualities and durability of planar or 3D in vivo electrode implants will require developing approaches to eliminate the insulating microglia junctions.
format Online
Article
Text
id pubmed-8645653
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-86456532021-12-07 Ultrastructural Analysis of Neuroimplant-Parenchyma Interfaces Uncover Remarkable Neuroregeneration Along-With Barriers That Limit the Implant Electrophysiological Functions Sharon, Aviv Shmoel, Nava Erez, Hadas Jankowski, Maciej M. Friedmann, Yael Spira, Micha E. Front Neurosci Neuroscience Despite increasing use of in vivo multielectrode array (MEA) implants for basic research and medical applications, the critical structural interfaces formed between the implants and the brain parenchyma, remain elusive. Prevailing view assumes that formation of multicellular inflammatory encapsulating-scar around the implants [the foreign body response (FBR)] degrades the implant electrophysiological functions. Using gold mushroom shaped microelectrodes (gMμEs) based perforated polyimide MEA platforms (PPMPs) that in contrast to standard probes can be thin sectioned along with the interfacing parenchyma; we examined here for the first time the interfaces formed between brains parenchyma and implanted 3D vertical microelectrode platforms at the ultrastructural level. Our study demonstrates remarkable regenerative processes including neuritogenesis, axon myelination, synapse formation and capillaries regrowth in contact and around the implant. In parallel, we document that individual microglia adhere tightly and engulf the gMμEs. Modeling of the formed microglia-electrode junctions suggest that this configuration suffice to account for the low and deteriorating recording qualities of in vivo MEA implants. These observations help define the anticipated hurdles to adapting the advantageous 3D in vitro vertical-electrode technologies to in vivo settings, and suggest that improving the recording qualities and durability of planar or 3D in vivo electrode implants will require developing approaches to eliminate the insulating microglia junctions. Frontiers Media S.A. 2021-11-22 /pmc/articles/PMC8645653/ /pubmed/34880722 http://dx.doi.org/10.3389/fnins.2021.764448 Text en Copyright © 2021 Sharon, Shmoel, Erez, Jankowski, Friedmann and Spira. https://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 or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) 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
Sharon, Aviv
Shmoel, Nava
Erez, Hadas
Jankowski, Maciej M.
Friedmann, Yael
Spira, Micha E.
Ultrastructural Analysis of Neuroimplant-Parenchyma Interfaces Uncover Remarkable Neuroregeneration Along-With Barriers That Limit the Implant Electrophysiological Functions
title Ultrastructural Analysis of Neuroimplant-Parenchyma Interfaces Uncover Remarkable Neuroregeneration Along-With Barriers That Limit the Implant Electrophysiological Functions
title_full Ultrastructural Analysis of Neuroimplant-Parenchyma Interfaces Uncover Remarkable Neuroregeneration Along-With Barriers That Limit the Implant Electrophysiological Functions
title_fullStr Ultrastructural Analysis of Neuroimplant-Parenchyma Interfaces Uncover Remarkable Neuroregeneration Along-With Barriers That Limit the Implant Electrophysiological Functions
title_full_unstemmed Ultrastructural Analysis of Neuroimplant-Parenchyma Interfaces Uncover Remarkable Neuroregeneration Along-With Barriers That Limit the Implant Electrophysiological Functions
title_short Ultrastructural Analysis of Neuroimplant-Parenchyma Interfaces Uncover Remarkable Neuroregeneration Along-With Barriers That Limit the Implant Electrophysiological Functions
title_sort ultrastructural analysis of neuroimplant-parenchyma interfaces uncover remarkable neuroregeneration along-with barriers that limit the implant electrophysiological functions
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645653/
https://www.ncbi.nlm.nih.gov/pubmed/34880722
http://dx.doi.org/10.3389/fnins.2021.764448
work_keys_str_mv AT sharonaviv ultrastructuralanalysisofneuroimplantparenchymainterfacesuncoverremarkableneuroregenerationalongwithbarriersthatlimittheimplantelectrophysiologicalfunctions
AT shmoelnava ultrastructuralanalysisofneuroimplantparenchymainterfacesuncoverremarkableneuroregenerationalongwithbarriersthatlimittheimplantelectrophysiologicalfunctions
AT erezhadas ultrastructuralanalysisofneuroimplantparenchymainterfacesuncoverremarkableneuroregenerationalongwithbarriersthatlimittheimplantelectrophysiologicalfunctions
AT jankowskimaciejm ultrastructuralanalysisofneuroimplantparenchymainterfacesuncoverremarkableneuroregenerationalongwithbarriersthatlimittheimplantelectrophysiologicalfunctions
AT friedmannyael ultrastructuralanalysisofneuroimplantparenchymainterfacesuncoverremarkableneuroregenerationalongwithbarriersthatlimittheimplantelectrophysiologicalfunctions
AT spiramichae ultrastructuralanalysisofneuroimplantparenchymainterfacesuncoverremarkableneuroregenerationalongwithbarriersthatlimittheimplantelectrophysiologicalfunctions