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Oxygen gradient generator to improve in vitro modeling of ischemic stroke
INTRODUCTION: In the core of a brain infarct, perfusion is severely impeded, and neuronal death occurs within minutes. In the penumbra, an area near the core with more remaining perfusion, cells initially remain viable, but activity is significantly reduced. In principle, the penumbra can be saved i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086255/ https://www.ncbi.nlm.nih.gov/pubmed/37056304 http://dx.doi.org/10.3389/fnins.2023.1110083 |
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author | Santiago, João Kreutzer, Joose Bossink, Elsbeth Kallio, Pasi le Feber, Joost |
author_facet | Santiago, João Kreutzer, Joose Bossink, Elsbeth Kallio, Pasi le Feber, Joost |
author_sort | Santiago, João |
collection | PubMed |
description | INTRODUCTION: In the core of a brain infarct, perfusion is severely impeded, and neuronal death occurs within minutes. In the penumbra, an area near the core with more remaining perfusion, cells initially remain viable, but activity is significantly reduced. In principle, the penumbra can be saved if reperfusion is established on time, making it a promising target for treatment. In vitro models with cultured neurons on microelectrode arrays (MEAs) provide a useful tool to investigate how ischemic stroke affects neuronal functioning. These models tend to be uniform, focusing on the isolated penumbra, and typically lack adjacent regions such as a core and unaffected regions (normal perfusion). However, processes in these regions may affect neuronal functioning and survival in the penumbra. MATERIALS AND METHODS: Here, we designed, fabricated, and characterized a cytocompatible device that generates an oxygen gradient across in vitro neuronal cultures to expose cells to hypoxia of various depths from near anoxia to near normoxia. This marks a step in the path to mimic core, penumbra, and healthy tissue, and will facilitate better in vitro modeling of ischemic stroke. RESULTS: The generator forms a stable and reproducible gradient within 30 min. Oxygen concentrations at the extremes are adjustable in a physiologically relevant range. Application of the generator did not negatively affect electrophysiological recordings or the viability of cultures, thus confirming the cytocompatibility of the device. DISCUSSION: The developed device is able to impose an oxygen gradient on neuronal cultures and may enrich in vitro stroke models. |
format | Online Article Text |
id | pubmed-10086255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100862552023-04-12 Oxygen gradient generator to improve in vitro modeling of ischemic stroke Santiago, João Kreutzer, Joose Bossink, Elsbeth Kallio, Pasi le Feber, Joost Front Neurosci Neuroscience INTRODUCTION: In the core of a brain infarct, perfusion is severely impeded, and neuronal death occurs within minutes. In the penumbra, an area near the core with more remaining perfusion, cells initially remain viable, but activity is significantly reduced. In principle, the penumbra can be saved if reperfusion is established on time, making it a promising target for treatment. In vitro models with cultured neurons on microelectrode arrays (MEAs) provide a useful tool to investigate how ischemic stroke affects neuronal functioning. These models tend to be uniform, focusing on the isolated penumbra, and typically lack adjacent regions such as a core and unaffected regions (normal perfusion). However, processes in these regions may affect neuronal functioning and survival in the penumbra. MATERIALS AND METHODS: Here, we designed, fabricated, and characterized a cytocompatible device that generates an oxygen gradient across in vitro neuronal cultures to expose cells to hypoxia of various depths from near anoxia to near normoxia. This marks a step in the path to mimic core, penumbra, and healthy tissue, and will facilitate better in vitro modeling of ischemic stroke. RESULTS: The generator forms a stable and reproducible gradient within 30 min. Oxygen concentrations at the extremes are adjustable in a physiologically relevant range. Application of the generator did not negatively affect electrophysiological recordings or the viability of cultures, thus confirming the cytocompatibility of the device. DISCUSSION: The developed device is able to impose an oxygen gradient on neuronal cultures and may enrich in vitro stroke models. Frontiers Media S.A. 2023-03-28 /pmc/articles/PMC10086255/ /pubmed/37056304 http://dx.doi.org/10.3389/fnins.2023.1110083 Text en Copyright © 2023 Santiago, Kreutzer, Bossink, Kallio and le Feber. 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 Santiago, João Kreutzer, Joose Bossink, Elsbeth Kallio, Pasi le Feber, Joost Oxygen gradient generator to improve in vitro modeling of ischemic stroke |
title | Oxygen gradient generator to improve in vitro modeling of ischemic stroke |
title_full | Oxygen gradient generator to improve in vitro modeling of ischemic stroke |
title_fullStr | Oxygen gradient generator to improve in vitro modeling of ischemic stroke |
title_full_unstemmed | Oxygen gradient generator to improve in vitro modeling of ischemic stroke |
title_short | Oxygen gradient generator to improve in vitro modeling of ischemic stroke |
title_sort | oxygen gradient generator to improve in vitro modeling of ischemic stroke |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086255/ https://www.ncbi.nlm.nih.gov/pubmed/37056304 http://dx.doi.org/10.3389/fnins.2023.1110083 |
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