Cargando…
Neuromuscular disease modeling on a chip
Organs-on-chips are broadly defined as microfabricated surfaces or devices designed to engineer cells into microscale tissues with native-like features and then extract physiologically relevant readouts at scale. Because they are generally compatible with patient-derived cells, these technologies ca...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7358135/ https://www.ncbi.nlm.nih.gov/pubmed/32817118 http://dx.doi.org/10.1242/dmm.044867 |
_version_ | 1783558791245070336 |
---|---|
author | Santoso, Jeffrey W. McCain, Megan L. |
author_facet | Santoso, Jeffrey W. McCain, Megan L. |
author_sort | Santoso, Jeffrey W. |
collection | PubMed |
description | Organs-on-chips are broadly defined as microfabricated surfaces or devices designed to engineer cells into microscale tissues with native-like features and then extract physiologically relevant readouts at scale. Because they are generally compatible with patient-derived cells, these technologies can address many of the human relevance limitations of animal models. As a result, organs-on-chips have emerged as a promising new paradigm for patient-specific disease modeling and drug development. Because neuromuscular diseases span a broad range of rare conditions with diverse etiology and complex pathophysiology, they have been especially challenging to model in animals and thus are well suited for organ-on-chip approaches. In this Review, we first briefly summarize the challenges in neuromuscular disease modeling with animal models. Next, we describe a variety of existing organ-on-chip approaches for neuromuscular tissues, including a survey of cell sources for both muscle and nerve, and two- and three-dimensional neuromuscular tissue-engineering techniques. Although researchers have made tremendous advances in modeling neuromuscular diseases on a chip, the remaining challenges in cell sourcing, cell maturity, tissue assembly and readout capabilities limit their integration into the drug development pipeline today. However, as the field advances, models of healthy and diseased neuromuscular tissues on a chip, coupled with animal models, have vast potential as complementary tools for modeling multiple aspects of neuromuscular diseases and identifying new therapeutic strategies. |
format | Online Article Text |
id | pubmed-7358135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-73581352020-07-14 Neuromuscular disease modeling on a chip Santoso, Jeffrey W. McCain, Megan L. Dis Model Mech Review Organs-on-chips are broadly defined as microfabricated surfaces or devices designed to engineer cells into microscale tissues with native-like features and then extract physiologically relevant readouts at scale. Because they are generally compatible with patient-derived cells, these technologies can address many of the human relevance limitations of animal models. As a result, organs-on-chips have emerged as a promising new paradigm for patient-specific disease modeling and drug development. Because neuromuscular diseases span a broad range of rare conditions with diverse etiology and complex pathophysiology, they have been especially challenging to model in animals and thus are well suited for organ-on-chip approaches. In this Review, we first briefly summarize the challenges in neuromuscular disease modeling with animal models. Next, we describe a variety of existing organ-on-chip approaches for neuromuscular tissues, including a survey of cell sources for both muscle and nerve, and two- and three-dimensional neuromuscular tissue-engineering techniques. Although researchers have made tremendous advances in modeling neuromuscular diseases on a chip, the remaining challenges in cell sourcing, cell maturity, tissue assembly and readout capabilities limit their integration into the drug development pipeline today. However, as the field advances, models of healthy and diseased neuromuscular tissues on a chip, coupled with animal models, have vast potential as complementary tools for modeling multiple aspects of neuromuscular diseases and identifying new therapeutic strategies. The Company of Biologists Ltd 2020-07-07 /pmc/articles/PMC7358135/ /pubmed/32817118 http://dx.doi.org/10.1242/dmm.044867 Text en © 2020. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Review Santoso, Jeffrey W. McCain, Megan L. Neuromuscular disease modeling on a chip |
title | Neuromuscular disease modeling on a chip |
title_full | Neuromuscular disease modeling on a chip |
title_fullStr | Neuromuscular disease modeling on a chip |
title_full_unstemmed | Neuromuscular disease modeling on a chip |
title_short | Neuromuscular disease modeling on a chip |
title_sort | neuromuscular disease modeling on a chip |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7358135/ https://www.ncbi.nlm.nih.gov/pubmed/32817118 http://dx.doi.org/10.1242/dmm.044867 |
work_keys_str_mv | AT santosojeffreyw neuromusculardiseasemodelingonachip AT mccainmeganl neuromusculardiseasemodelingonachip |