Cardiac Cell Patterning on Customized Microelectrode Arrays for Electrophysiological Recordings

Cardiomyocytes (CMs) and fibroblast cells are two essential elements for cardiac tissue structure and function. The interactions between them can alter cardiac electrophysiology and thus contribute to cardiac diseases, such as arrhythmogenesis. One possible explanation is that fibroblasts can direct...

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Autores principales: Jiaying Ji, Xiang Ren, Pinar Zorlutuna
Formato: article
Lenguaje:EN
Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/dd269cc0826c4af7b7611e1b68d77e8d
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spelling oai:doaj.org-article:dd269cc0826c4af7b7611e1b68d77e8d2021-11-25T18:23:20ZCardiac Cell Patterning on Customized Microelectrode Arrays for Electrophysiological Recordings10.3390/mi121113512072-666Xhttps://doaj.org/article/dd269cc0826c4af7b7611e1b68d77e8d2021-10-01T00:00:00Zhttps://www.mdpi.com/2072-666X/12/11/1351https://doaj.org/toc/2072-666XCardiomyocytes (CMs) and fibroblast cells are two essential elements for cardiac tissue structure and function. The interactions between them can alter cardiac electrophysiology and thus contribute to cardiac diseases, such as arrhythmogenesis. One possible explanation is that fibroblasts can directly affect cardiac electrophysiology through electrical coupling with CMs. Therefore, detecting the electrical activities in the CM-fibroblast network is vital for understanding the coupling dynamics among them. Current commercialized platforms for studying cardiac electrophysiology utilize planar microelectrode arrays (MEAs) to record the extracellular field potential (FP) in real-time, but the prearranged electrode configuration highly limits the measurement capabilities at specific locations. Here, we report a custom-designed MEA device with a novel micropatterning method to construct a controlled network of neonatal rat CMs (rCMs) and fibroblast connections for monitoring the electrical activity of rCM-fibroblast co-cultures in a spatially controlled fashion. For the micropatterning of the co-culture, surface topographical features and mobile blockers were used to control the initial attachment locations of a mixture of rCMs and fibroblasts, to form separate beating rCM-fibroblast clusters while leaving empty space for fibroblast growth to connect these clusters. Once the blockers are removed, the proliferating fibroblasts connect and couple the separate beating clusters. Using this method, electrical activity of both rCMs and human-induced-pluripotent-stem-cell-derived cardiomyocytes (iCMs) was examined. The coupling dynamics were studied through the extracellular FP and impedance profile recorded from the MEA device, indicating that the fibroblast bridge provided an RC-type coupling of physically separate rCM-containing clusters and enabled synchronization of these clusters.Jiaying JiXiang RenPinar ZorlutunaMDPI AGarticlemicroelectrode arraycardiomyocyteshuman pluripotent stem cellsmicro-patterningMechanical engineering and machineryTJ1-1570ENMicromachines, Vol 12, Iss 1351, p 1351 (2021)
institution DOAJ
collection DOAJ
language EN
topic microelectrode array
cardiomyocytes
human pluripotent stem cells
micro-patterning
Mechanical engineering and machinery
TJ1-1570
spellingShingle microelectrode array
cardiomyocytes
human pluripotent stem cells
micro-patterning
Mechanical engineering and machinery
TJ1-1570
Jiaying Ji
Xiang Ren
Pinar Zorlutuna
Cardiac Cell Patterning on Customized Microelectrode Arrays for Electrophysiological Recordings
description Cardiomyocytes (CMs) and fibroblast cells are two essential elements for cardiac tissue structure and function. The interactions between them can alter cardiac electrophysiology and thus contribute to cardiac diseases, such as arrhythmogenesis. One possible explanation is that fibroblasts can directly affect cardiac electrophysiology through electrical coupling with CMs. Therefore, detecting the electrical activities in the CM-fibroblast network is vital for understanding the coupling dynamics among them. Current commercialized platforms for studying cardiac electrophysiology utilize planar microelectrode arrays (MEAs) to record the extracellular field potential (FP) in real-time, but the prearranged electrode configuration highly limits the measurement capabilities at specific locations. Here, we report a custom-designed MEA device with a novel micropatterning method to construct a controlled network of neonatal rat CMs (rCMs) and fibroblast connections for monitoring the electrical activity of rCM-fibroblast co-cultures in a spatially controlled fashion. For the micropatterning of the co-culture, surface topographical features and mobile blockers were used to control the initial attachment locations of a mixture of rCMs and fibroblasts, to form separate beating rCM-fibroblast clusters while leaving empty space for fibroblast growth to connect these clusters. Once the blockers are removed, the proliferating fibroblasts connect and couple the separate beating clusters. Using this method, electrical activity of both rCMs and human-induced-pluripotent-stem-cell-derived cardiomyocytes (iCMs) was examined. The coupling dynamics were studied through the extracellular FP and impedance profile recorded from the MEA device, indicating that the fibroblast bridge provided an RC-type coupling of physically separate rCM-containing clusters and enabled synchronization of these clusters.
format article
author Jiaying Ji
Xiang Ren
Pinar Zorlutuna
author_facet Jiaying Ji
Xiang Ren
Pinar Zorlutuna
author_sort Jiaying Ji
title Cardiac Cell Patterning on Customized Microelectrode Arrays for Electrophysiological Recordings
title_short Cardiac Cell Patterning on Customized Microelectrode Arrays for Electrophysiological Recordings
title_full Cardiac Cell Patterning on Customized Microelectrode Arrays for Electrophysiological Recordings
title_fullStr Cardiac Cell Patterning on Customized Microelectrode Arrays for Electrophysiological Recordings
title_full_unstemmed Cardiac Cell Patterning on Customized Microelectrode Arrays for Electrophysiological Recordings
title_sort cardiac cell patterning on customized microelectrode arrays for electrophysiological recordings
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/dd269cc0826c4af7b7611e1b68d77e8d
work_keys_str_mv AT jiayingji cardiaccellpatterningoncustomizedmicroelectrodearraysforelectrophysiologicalrecordings
AT xiangren cardiaccellpatterningoncustomizedmicroelectrodearraysforelectrophysiologicalrecordings
AT pinarzorlutuna cardiaccellpatterningoncustomizedmicroelectrodearraysforelectrophysiologicalrecordings
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