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Adventures and Advances in Time Travel With Induced Pluripotent Stem Cells and Automated Patch Clamp
In the Hollywood blockbuster “The Curious Case of Benjamin Button” a fantastical fable unfolds of a man’s life that travels through time reversing the aging process; as the tale progresses, the frail old man becomes a vigorous, vivacious young man, then man becomes boy and boy becomes baby. The real...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258620/ https://www.ncbi.nlm.nih.gov/pubmed/35813069 http://dx.doi.org/10.3389/fnmol.2022.898717 |
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author | Rosholm, Kadla R. Badone, Beatrice Karatsiompani, Stefania Nagy, David Seibertz, Fitzwilliam Voigt, Niels Bell, Damian C. |
author_facet | Rosholm, Kadla R. Badone, Beatrice Karatsiompani, Stefania Nagy, David Seibertz, Fitzwilliam Voigt, Niels Bell, Damian C. |
author_sort | Rosholm, Kadla R. |
collection | PubMed |
description | In the Hollywood blockbuster “The Curious Case of Benjamin Button” a fantastical fable unfolds of a man’s life that travels through time reversing the aging process; as the tale progresses, the frail old man becomes a vigorous, vivacious young man, then man becomes boy and boy becomes baby. The reality of cellular time travel, however, is far more wondrous: we now have the ability to both reverse and then forward time on mature cells. Four proteins were found to rewind the molecular clock of adult cells back to their embryonic, “blank canvas” pluripotent stem cell state, allowing these pluripotent stem cells to then be differentiated to fast forward their molecular clocks to the desired adult specialist cell types. These four proteins – the “Yamanaka factors” – form critical elements of this cellular time travel, which deservedly won Shinya Yamanaka the Nobel Prize for his lab’s work discovering them. Human induced pluripotent stem cells (hiPSCs) hold much promise in our understanding of physiology and medicine. They encapsulate the signaling pathways of the desired cell types, such as cardiomyocytes or neurons, and thus act as model cells for defining the critical ion channel activity in healthy and disease states. Since hiPSCs can be derived from any patient, highly specific, personalized (or stratified) physiology, and/or pathophysiology can be defined, leading to exciting developments in personalized medicines and interventions. As such, hiPSC married with high throughput automated patch clamp (APC) ion channel recording platforms provide a foundation for significant physiological, medical and drug discovery advances. This review aims to summarize the current state of affairs of hiPSC and APC: the background and recent advances made; and the pros, cons and challenges of these technologies. Whilst the authors have yet to finalize a fully functional time traveling machine, they will endeavor to provide plausible future projections on where hiPSC and APC are likely to carry us. One future projection the authors are confident in making is the increasing necessity and adoption of these technologies in the discovery of the next blockbuster, this time a life-enhancing ion channel drug, not a fantastical movie. |
format | Online Article Text |
id | pubmed-9258620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92586202022-07-07 Adventures and Advances in Time Travel With Induced Pluripotent Stem Cells and Automated Patch Clamp Rosholm, Kadla R. Badone, Beatrice Karatsiompani, Stefania Nagy, David Seibertz, Fitzwilliam Voigt, Niels Bell, Damian C. Front Mol Neurosci Neuroscience In the Hollywood blockbuster “The Curious Case of Benjamin Button” a fantastical fable unfolds of a man’s life that travels through time reversing the aging process; as the tale progresses, the frail old man becomes a vigorous, vivacious young man, then man becomes boy and boy becomes baby. The reality of cellular time travel, however, is far more wondrous: we now have the ability to both reverse and then forward time on mature cells. Four proteins were found to rewind the molecular clock of adult cells back to their embryonic, “blank canvas” pluripotent stem cell state, allowing these pluripotent stem cells to then be differentiated to fast forward their molecular clocks to the desired adult specialist cell types. These four proteins – the “Yamanaka factors” – form critical elements of this cellular time travel, which deservedly won Shinya Yamanaka the Nobel Prize for his lab’s work discovering them. Human induced pluripotent stem cells (hiPSCs) hold much promise in our understanding of physiology and medicine. They encapsulate the signaling pathways of the desired cell types, such as cardiomyocytes or neurons, and thus act as model cells for defining the critical ion channel activity in healthy and disease states. Since hiPSCs can be derived from any patient, highly specific, personalized (or stratified) physiology, and/or pathophysiology can be defined, leading to exciting developments in personalized medicines and interventions. As such, hiPSC married with high throughput automated patch clamp (APC) ion channel recording platforms provide a foundation for significant physiological, medical and drug discovery advances. This review aims to summarize the current state of affairs of hiPSC and APC: the background and recent advances made; and the pros, cons and challenges of these technologies. Whilst the authors have yet to finalize a fully functional time traveling machine, they will endeavor to provide plausible future projections on where hiPSC and APC are likely to carry us. One future projection the authors are confident in making is the increasing necessity and adoption of these technologies in the discovery of the next blockbuster, this time a life-enhancing ion channel drug, not a fantastical movie. Frontiers Media S.A. 2022-06-22 /pmc/articles/PMC9258620/ /pubmed/35813069 http://dx.doi.org/10.3389/fnmol.2022.898717 Text en Copyright © 2022 Rosholm, Badone, Karatsiompani, Nagy, Seibertz, Voigt and Bell. https://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 | Neuroscience Rosholm, Kadla R. Badone, Beatrice Karatsiompani, Stefania Nagy, David Seibertz, Fitzwilliam Voigt, Niels Bell, Damian C. Adventures and Advances in Time Travel With Induced Pluripotent Stem Cells and Automated Patch Clamp |
title | Adventures and Advances in Time Travel With Induced Pluripotent Stem Cells and Automated Patch Clamp |
title_full | Adventures and Advances in Time Travel With Induced Pluripotent Stem Cells and Automated Patch Clamp |
title_fullStr | Adventures and Advances in Time Travel With Induced Pluripotent Stem Cells and Automated Patch Clamp |
title_full_unstemmed | Adventures and Advances in Time Travel With Induced Pluripotent Stem Cells and Automated Patch Clamp |
title_short | Adventures and Advances in Time Travel With Induced Pluripotent Stem Cells and Automated Patch Clamp |
title_sort | adventures and advances in time travel with induced pluripotent stem cells and automated patch clamp |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258620/ https://www.ncbi.nlm.nih.gov/pubmed/35813069 http://dx.doi.org/10.3389/fnmol.2022.898717 |
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