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...

Full description

Bibliographic Details
Main Authors: Onur Aydin, Austin P. Passaro, Mohamed Elhebeary, Gelson J. Pagan-Diaz, Anthony Fan, Sittinon Nuethong, Rashid Bashir, Steven L. Stice, M. Taher A. Saif
Format: Article
Language:English
Published: AIP Publishing LLC 2020-03-01
Series:APL Bioengineering
Online Access:http://dx.doi.org/10.1063/1.5134477
id doaj-874ca6259732486996b215294e053ffa
record_format Article
spelling doaj-874ca6259732486996b215294e053ffa2020-11-25T03:20:18ZengAIP Publishing LLCAPL Bioengineering2473-28772020-03-0141016107016107-910.1063/1.5134477Development of 3D neuromuscular bioactuatorsOnur Aydin0Austin P. Passaro1Mohamed Elhebeary2Gelson J. Pagan-Diaz3Anthony Fan4Sittinon Nuethong5Rashid Bashir6Steven L. Stice7M. Taher A. Saif8 Department of Mechanical Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA Regenerative Bioscience Center, University of Georgia, Athens, Georgia 30602, USA Department of Mechanical Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA Department of Mechanical Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA Department of Mechanical Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA Regenerative Bioscience Center, University of Georgia, Athens, Georgia 30602, USA Department of Mechanical Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USANeuronal 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.http://dx.doi.org/10.1063/1.5134477
collection DOAJ
language English
format Article
sources DOAJ
author Onur Aydin
Austin P. Passaro
Mohamed Elhebeary
Gelson J. Pagan-Diaz
Anthony Fan
Sittinon Nuethong
Rashid Bashir
Steven L. Stice
M. Taher A. Saif
spellingShingle Onur Aydin
Austin P. Passaro
Mohamed Elhebeary
Gelson J. Pagan-Diaz
Anthony Fan
Sittinon Nuethong
Rashid Bashir
Steven L. Stice
M. Taher A. Saif
Development of 3D neuromuscular bioactuators
APL Bioengineering
author_facet Onur Aydin
Austin P. Passaro
Mohamed Elhebeary
Gelson J. Pagan-Diaz
Anthony Fan
Sittinon Nuethong
Rashid Bashir
Steven L. Stice
M. Taher A. Saif
author_sort Onur Aydin
title Development of 3D neuromuscular bioactuators
title_short 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_sort development of 3d neuromuscular bioactuators
publisher AIP Publishing LLC
series APL Bioengineering
issn 2473-2877
publishDate 2020-03-01
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.
url http://dx.doi.org/10.1063/1.5134477
work_keys_str_mv AT onuraydin developmentof3dneuromuscularbioactuators
AT austinppassaro developmentof3dneuromuscularbioactuators
AT mohamedelhebeary developmentof3dneuromuscularbioactuators
AT gelsonjpagandiaz developmentof3dneuromuscularbioactuators
AT anthonyfan developmentof3dneuromuscularbioactuators
AT sittinonnuethong developmentof3dneuromuscularbioactuators
AT rashidbashir developmentof3dneuromuscularbioactuators
AT stevenlstice developmentof3dneuromuscularbioactuators
AT mtaherasaif developmentof3dneuromuscularbioactuators
_version_ 1724618197424930816