Cargando…
Challenges in Physiological Phenotyping of hiPSC-Derived Neurons: From 2D Cultures to 3D Brain Organoids
Neurons derived from human induced pluripotent stem cells (hiPSC-derived neurons) offer novel opportunities for the development of preclinical models of human neurodegenerative diseases (NDDs). Recent advances in the past few years have increased substantially the potential of these techniques and h...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7479826/ https://www.ncbi.nlm.nih.gov/pubmed/32984317 http://dx.doi.org/10.3389/fcell.2020.00797 |
_version_ | 1783580331590287360 |
---|---|
author | Mateos-Aparicio, Pedro Bello, Sabina A. Rodríguez-Moreno, Antonio |
author_facet | Mateos-Aparicio, Pedro Bello, Sabina A. Rodríguez-Moreno, Antonio |
author_sort | Mateos-Aparicio, Pedro |
collection | PubMed |
description | Neurons derived from human induced pluripotent stem cells (hiPSC-derived neurons) offer novel opportunities for the development of preclinical models of human neurodegenerative diseases (NDDs). Recent advances in the past few years have increased substantially the potential of these techniques and have uncovered new challenges that the field is facing. Here, we outline and discuss challenges related to the functional characterization of hiPSC-derived neurons and propose ways to overcome current difficulties. In particular, the enormous variability among studies in the electrical properties of hiPSC-derived neurons and broad differences in cell maturation are factors that impair reproducibility. Furthermore, we discuss how the use of 3D brain organoids are of help in resolving some difficulties posed by 2D cultures. Finally, we elaborate on recent and future advances that may help to overcome the discussed challenges and speed-up progress in the field. |
format | Online Article Text |
id | pubmed-7479826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74798262020-09-26 Challenges in Physiological Phenotyping of hiPSC-Derived Neurons: From 2D Cultures to 3D Brain Organoids Mateos-Aparicio, Pedro Bello, Sabina A. Rodríguez-Moreno, Antonio Front Cell Dev Biol Cell and Developmental Biology Neurons derived from human induced pluripotent stem cells (hiPSC-derived neurons) offer novel opportunities for the development of preclinical models of human neurodegenerative diseases (NDDs). Recent advances in the past few years have increased substantially the potential of these techniques and have uncovered new challenges that the field is facing. Here, we outline and discuss challenges related to the functional characterization of hiPSC-derived neurons and propose ways to overcome current difficulties. In particular, the enormous variability among studies in the electrical properties of hiPSC-derived neurons and broad differences in cell maturation are factors that impair reproducibility. Furthermore, we discuss how the use of 3D brain organoids are of help in resolving some difficulties posed by 2D cultures. Finally, we elaborate on recent and future advances that may help to overcome the discussed challenges and speed-up progress in the field. Frontiers Media S.A. 2020-08-26 /pmc/articles/PMC7479826/ /pubmed/32984317 http://dx.doi.org/10.3389/fcell.2020.00797 Text en Copyright © 2020 Mateos-Aparicio, Bello and Rodríguez-Moreno. 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 | Cell and Developmental Biology Mateos-Aparicio, Pedro Bello, Sabina A. Rodríguez-Moreno, Antonio Challenges in Physiological Phenotyping of hiPSC-Derived Neurons: From 2D Cultures to 3D Brain Organoids |
title | Challenges in Physiological Phenotyping of hiPSC-Derived Neurons: From 2D Cultures to 3D Brain Organoids |
title_full | Challenges in Physiological Phenotyping of hiPSC-Derived Neurons: From 2D Cultures to 3D Brain Organoids |
title_fullStr | Challenges in Physiological Phenotyping of hiPSC-Derived Neurons: From 2D Cultures to 3D Brain Organoids |
title_full_unstemmed | Challenges in Physiological Phenotyping of hiPSC-Derived Neurons: From 2D Cultures to 3D Brain Organoids |
title_short | Challenges in Physiological Phenotyping of hiPSC-Derived Neurons: From 2D Cultures to 3D Brain Organoids |
title_sort | challenges in physiological phenotyping of hipsc-derived neurons: from 2d cultures to 3d brain organoids |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7479826/ https://www.ncbi.nlm.nih.gov/pubmed/32984317 http://dx.doi.org/10.3389/fcell.2020.00797 |
work_keys_str_mv | AT mateosapariciopedro challengesinphysiologicalphenotypingofhipscderivedneuronsfrom2dculturesto3dbrainorganoids AT bellosabinaa challengesinphysiologicalphenotypingofhipscderivedneuronsfrom2dculturesto3dbrainorganoids AT rodriguezmorenoantonio challengesinphysiologicalphenotypingofhipscderivedneuronsfrom2dculturesto3dbrainorganoids |