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A micro-fabricated in vitro complex neuronal circuit platform

Developments in micro-manufacture as well as biofabrication technologies are driving our ability to create complex tissue models such as ‘organ-on-a-chip’ devices. The complexity of neural tissue, however, requires precisely specific cellular connectivity across many neuronal populations, and thus t...

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Autores principales: Kamudzandu, M, Köse-Dunn, M, Evans, M G, Fricker, R A, Roach, P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOP Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208576/
http://dx.doi.org/10.1088/2057-1976/ab2307
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author Kamudzandu, M
Köse-Dunn, M
Evans, M G
Fricker, R A
Roach, P
author_facet Kamudzandu, M
Köse-Dunn, M
Evans, M G
Fricker, R A
Roach, P
author_sort Kamudzandu, M
collection PubMed
description Developments in micro-manufacture as well as biofabrication technologies are driving our ability to create complex tissue models such as ‘organ-on-a-chip’ devices. The complexity of neural tissue, however, requires precisely specific cellular connectivity across many neuronal populations, and thus there have been limited reports of complex ‘brain-on-a-chip’ technologies modelling specific cellular circuit function. Here we describe the development of a model of in vitro brain circuitry designed to accurately reproduce part of the complex circuitry involved in neurodegenerative diseases; using segregated co-culture of specific basal ganglia (BG) neuronal subtypes to model central nervous system circuitry. Lithographic methods and chemical modification were used to form structured micro-channels, which were populated by specifically cultured neuronal sub-types to represent parts of the inter-communicating neural circuit. Cell morphological assessment and immunostaining showed connectivity, which was supported by electrophysiology measurements. Electrical activity of cells was measured using patch-clamp, showing voltage dependant Na(+) and K(+) currents, and blocking of Na(+) current by TTX, and calcium imaging showing TTX-sensitive slow Ca(2+) oscillations resulting from action potentials. Monitoring cells across connected ports post-TTX addition demonstrated both upstream and downstream changes in activity, indicating network connectivity. The model developed herein provides a platform technology that could be used to better understand neurological function and dysfunction, contributing to a growing urgency for better treatments of neurodegenerative disease. We anticipate the use of this advancing technology for the assessment of pharmaceutical and cellular therapies as a means of pre-clinical assessment, and further for the advancement of neural engineering approaches for tissue engineering.
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spelling pubmed-82085762021-06-17 A micro-fabricated in vitro complex neuronal circuit platform Kamudzandu, M Köse-Dunn, M Evans, M G Fricker, R A Roach, P Biomed Phys Eng Express Paper Developments in micro-manufacture as well as biofabrication technologies are driving our ability to create complex tissue models such as ‘organ-on-a-chip’ devices. The complexity of neural tissue, however, requires precisely specific cellular connectivity across many neuronal populations, and thus there have been limited reports of complex ‘brain-on-a-chip’ technologies modelling specific cellular circuit function. Here we describe the development of a model of in vitro brain circuitry designed to accurately reproduce part of the complex circuitry involved in neurodegenerative diseases; using segregated co-culture of specific basal ganglia (BG) neuronal subtypes to model central nervous system circuitry. Lithographic methods and chemical modification were used to form structured micro-channels, which were populated by specifically cultured neuronal sub-types to represent parts of the inter-communicating neural circuit. Cell morphological assessment and immunostaining showed connectivity, which was supported by electrophysiology measurements. Electrical activity of cells was measured using patch-clamp, showing voltage dependant Na(+) and K(+) currents, and blocking of Na(+) current by TTX, and calcium imaging showing TTX-sensitive slow Ca(2+) oscillations resulting from action potentials. Monitoring cells across connected ports post-TTX addition demonstrated both upstream and downstream changes in activity, indicating network connectivity. The model developed herein provides a platform technology that could be used to better understand neurological function and dysfunction, contributing to a growing urgency for better treatments of neurodegenerative disease. We anticipate the use of this advancing technology for the assessment of pharmaceutical and cellular therapies as a means of pre-clinical assessment, and further for the advancement of neural engineering approaches for tissue engineering. IOP Publishing 2019-07 2019-06-03 /pmc/articles/PMC8208576/ http://dx.doi.org/10.1088/2057-1976/ab2307 Text en © 2019 IOP Publishing Ltd https://creativecommons.org/licenses/by/3.0/Original content from this work may be used under the terms of the Creative Commons Attribution 3.0 licence (https://creativecommons.org/licenses/by/3.0/) . Any further distribution of this work must maintain attribution to the author(s) and the title of the work, journal citation and DOI.
spellingShingle Paper
Kamudzandu, M
Köse-Dunn, M
Evans, M G
Fricker, R A
Roach, P
A micro-fabricated in vitro complex neuronal circuit platform
title A micro-fabricated in vitro complex neuronal circuit platform
title_full A micro-fabricated in vitro complex neuronal circuit platform
title_fullStr A micro-fabricated in vitro complex neuronal circuit platform
title_full_unstemmed A micro-fabricated in vitro complex neuronal circuit platform
title_short A micro-fabricated in vitro complex neuronal circuit platform
title_sort micro-fabricated in vitro complex neuronal circuit platform
topic Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208576/
http://dx.doi.org/10.1088/2057-1976/ab2307
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