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Challenges and Future Prospects on 3D in-vitro Modeling of the Neuromuscular Circuit

Movement of skeletal-muscle fibers is generated by the coordinated action of several cells taking part within the locomotion circuit (motoneurons, sensory-neurons, Schwann cells, astrocytes, microglia, and muscle-cells). Failures in any part of this circuit could impede or hinder coordinated muscle...

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Autores principales: Badiola-Mateos, Maider, Hervera, Arnau, del Río, José Antonio, Samitier, Josep
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6297173/
https://www.ncbi.nlm.nih.gov/pubmed/30622944
http://dx.doi.org/10.3389/fbioe.2018.00194
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author Badiola-Mateos, Maider
Hervera, Arnau
del Río, José Antonio
Samitier, Josep
author_facet Badiola-Mateos, Maider
Hervera, Arnau
del Río, José Antonio
Samitier, Josep
author_sort Badiola-Mateos, Maider
collection PubMed
description Movement of skeletal-muscle fibers is generated by the coordinated action of several cells taking part within the locomotion circuit (motoneurons, sensory-neurons, Schwann cells, astrocytes, microglia, and muscle-cells). Failures in any part of this circuit could impede or hinder coordinated muscle movement and cause a neuromuscular disease (NMD) or determine its severity. Studying fragments of the circuit cannot provide a comprehensive and complete view of the pathological process. We trace the historic developments of studies focused on in-vitro modeling of the spinal-locomotion circuit and how bioengineered innovative technologies show advantages for an accurate mimicking of physiological conditions of spinal-locomotion circuit. New developments on compartmentalized microfluidic culture systems (cμFCS), the use of human induced pluripotent stem cells (hiPSCs) and 3D cell-cultures are analyzed. We finally address limitations of current study models and three main challenges on neuromuscular studies: (i) mimic the whole spinal-locomotion circuit including all cell-types involved and the evaluation of independent and interdependent roles of each one; (ii) mimic the neurodegenerative response of mature neurons in-vitro as it occurs in-vivo; and (iii) develop, tune, implement, and combine cμFCS, hiPSC, and 3D-culture technologies to ultimately create patient-specific complete, translational, and reliable NMD in-vitro model. Overcoming these challenges would significantly facilitate understanding the events taking place in NMDs and accelerate the process of finding new therapies.
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spelling pubmed-62971732019-01-08 Challenges and Future Prospects on 3D in-vitro Modeling of the Neuromuscular Circuit Badiola-Mateos, Maider Hervera, Arnau del Río, José Antonio Samitier, Josep Front Bioeng Biotechnol Bioengineering and Biotechnology Movement of skeletal-muscle fibers is generated by the coordinated action of several cells taking part within the locomotion circuit (motoneurons, sensory-neurons, Schwann cells, astrocytes, microglia, and muscle-cells). Failures in any part of this circuit could impede or hinder coordinated muscle movement and cause a neuromuscular disease (NMD) or determine its severity. Studying fragments of the circuit cannot provide a comprehensive and complete view of the pathological process. We trace the historic developments of studies focused on in-vitro modeling of the spinal-locomotion circuit and how bioengineered innovative technologies show advantages for an accurate mimicking of physiological conditions of spinal-locomotion circuit. New developments on compartmentalized microfluidic culture systems (cμFCS), the use of human induced pluripotent stem cells (hiPSCs) and 3D cell-cultures are analyzed. We finally address limitations of current study models and three main challenges on neuromuscular studies: (i) mimic the whole spinal-locomotion circuit including all cell-types involved and the evaluation of independent and interdependent roles of each one; (ii) mimic the neurodegenerative response of mature neurons in-vitro as it occurs in-vivo; and (iii) develop, tune, implement, and combine cμFCS, hiPSC, and 3D-culture technologies to ultimately create patient-specific complete, translational, and reliable NMD in-vitro model. Overcoming these challenges would significantly facilitate understanding the events taking place in NMDs and accelerate the process of finding new therapies. Frontiers Media S.A. 2018-12-11 /pmc/articles/PMC6297173/ /pubmed/30622944 http://dx.doi.org/10.3389/fbioe.2018.00194 Text en Copyright © 2018 Badiola-Mateos, Hervera, del Río and Samitier. http://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 Bioengineering and Biotechnology
Badiola-Mateos, Maider
Hervera, Arnau
del Río, José Antonio
Samitier, Josep
Challenges and Future Prospects on 3D in-vitro Modeling of the Neuromuscular Circuit
title Challenges and Future Prospects on 3D in-vitro Modeling of the Neuromuscular Circuit
title_full Challenges and Future Prospects on 3D in-vitro Modeling of the Neuromuscular Circuit
title_fullStr Challenges and Future Prospects on 3D in-vitro Modeling of the Neuromuscular Circuit
title_full_unstemmed Challenges and Future Prospects on 3D in-vitro Modeling of the Neuromuscular Circuit
title_short Challenges and Future Prospects on 3D in-vitro Modeling of the Neuromuscular Circuit
title_sort challenges and future prospects on 3d in-vitro modeling of the neuromuscular circuit
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6297173/
https://www.ncbi.nlm.nih.gov/pubmed/30622944
http://dx.doi.org/10.3389/fbioe.2018.00194
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