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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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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. |
format | Online Article Text |
id | pubmed-6297173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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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