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Development of 3D neuromuscular bioactuators
Neuronal control of skeletal muscle bioactuators represents a critical milestone toward the realization of future biohybrid machines that may generate complex motor patterns and autonomously navigate through their environment. Animals achieve these feats using neural networks that generate robust fi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AIP Publishing LLC
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7064368/ https://www.ncbi.nlm.nih.gov/pubmed/32161837 http://dx.doi.org/10.1063/1.5134477 |
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author | Aydin, Onur Passaro, Austin P. Elhebeary, Mohamed Pagan-Diaz, Gelson J. Fan, Anthony Nuethong, Sittinon Bashir, Rashid Stice, Steven L. Saif, M. Taher A. |
author_facet | Aydin, Onur Passaro, Austin P. Elhebeary, Mohamed Pagan-Diaz, Gelson J. Fan, Anthony Nuethong, Sittinon Bashir, Rashid Stice, Steven L. Saif, M. Taher A. |
author_sort | Aydin, Onur |
collection | PubMed |
description | Neuronal control of skeletal muscle bioactuators represents a critical milestone toward the realization of future biohybrid machines that may generate complex motor patterns and autonomously navigate through their environment. Animals achieve these feats using neural networks that generate robust firing patterns and coordinate muscle activity through neuromuscular units. Here, we designed a versatile 3D neuron-muscle co-culture platform to serve as a test-bed for neuromuscular bioactuators. We used our platform in conjunction with microelectrode array electrophysiology to study the roles of synergistic interactions in the co-development of neural networks and muscle tissues. Our platform design enables co-culture of a neuronal cluster with up to four target muscle actuators, as well as quantification of muscle contraction forces. Using engineered muscle tissue targets, we first demonstrated the formation of functional neuromuscular bioactuators. We then investigated possible roles of long-range interactions in neuronal outgrowth patterns and observed preferential outgrowth toward muscles compared to the acellular matrix or fibroblasts, indicating muscle-specific chemotactic cues acting on motor neurons. Next, we showed that co-cultured muscle strips exhibited significantly higher spontaneous contractility as well as improved sarcomere assembly compared to muscles cultured alone. Finally, we performed microelectrode array measurements on neuronal cultures, which revealed that muscle-conditioned medium enhances overall neural firing rates and the emergence of synchronous bursting patterns. Overall, our study illustrates the significance of neuron-muscle cross talk for the in vitro development of neuromuscular bioactuators. |
format | Online Article Text |
id | pubmed-7064368 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AIP Publishing LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-70643682020-03-11 Development of 3D neuromuscular bioactuators Aydin, Onur Passaro, Austin P. Elhebeary, Mohamed Pagan-Diaz, Gelson J. Fan, Anthony Nuethong, Sittinon Bashir, Rashid Stice, Steven L. Saif, M. Taher A. APL Bioeng Articles Neuronal control of skeletal muscle bioactuators represents a critical milestone toward the realization of future biohybrid machines that may generate complex motor patterns and autonomously navigate through their environment. Animals achieve these feats using neural networks that generate robust firing patterns and coordinate muscle activity through neuromuscular units. Here, we designed a versatile 3D neuron-muscle co-culture platform to serve as a test-bed for neuromuscular bioactuators. We used our platform in conjunction with microelectrode array electrophysiology to study the roles of synergistic interactions in the co-development of neural networks and muscle tissues. Our platform design enables co-culture of a neuronal cluster with up to four target muscle actuators, as well as quantification of muscle contraction forces. Using engineered muscle tissue targets, we first demonstrated the formation of functional neuromuscular bioactuators. We then investigated possible roles of long-range interactions in neuronal outgrowth patterns and observed preferential outgrowth toward muscles compared to the acellular matrix or fibroblasts, indicating muscle-specific chemotactic cues acting on motor neurons. Next, we showed that co-cultured muscle strips exhibited significantly higher spontaneous contractility as well as improved sarcomere assembly compared to muscles cultured alone. Finally, we performed microelectrode array measurements on neuronal cultures, which revealed that muscle-conditioned medium enhances overall neural firing rates and the emergence of synchronous bursting patterns. Overall, our study illustrates the significance of neuron-muscle cross talk for the in vitro development of neuromuscular bioactuators. AIP Publishing LLC 2020-03-10 /pmc/articles/PMC7064368/ /pubmed/32161837 http://dx.doi.org/10.1063/1.5134477 Text en © Author(s). 2473-2877/2020/4(1)/016107/9 All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Articles Aydin, Onur Passaro, Austin P. Elhebeary, Mohamed Pagan-Diaz, Gelson J. Fan, Anthony Nuethong, Sittinon Bashir, Rashid Stice, Steven L. Saif, M. Taher A. Development of 3D neuromuscular bioactuators |
title | Development of 3D neuromuscular bioactuators |
title_full | Development of 3D neuromuscular bioactuators |
title_fullStr | Development of 3D neuromuscular bioactuators |
title_full_unstemmed | Development of 3D neuromuscular bioactuators |
title_short | Development of 3D neuromuscular bioactuators |
title_sort | development of 3d neuromuscular bioactuators |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7064368/ https://www.ncbi.nlm.nih.gov/pubmed/32161837 http://dx.doi.org/10.1063/1.5134477 |
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