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Pattern of Functional TTX-Resistant Sodium Channels Reveals a Developmental Stage of Human iPSC- and ESC-Derived Nociceptors

Human pluripotent stem cells (hPSCs) offer the opportunity to generate neuronal cells, including nociceptors. Using a chemical-based approach, we generated nociceptive sensory neurons from HUES6 embryonic stem cells and retrovirally reprogrammed induced hPSCs derived from fibroblasts. The nociceptiv...

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Autores principales: Eberhardt, Esther, Havlicek, Steven, Schmidt, Diana, Link, Andrea S., Neacsu, Cristian, Kohl, Zacharias, Hampl, Martin, Kist, Andreas M., Klinger, Alexandra, Nau, Carla, Schüttler, Jürgen, Alzheimer, Christian, Winkler, Jürgen, Namer, Barbara, Winner, Beate, Lampert, Angelika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618592/
https://www.ncbi.nlm.nih.gov/pubmed/26321143
http://dx.doi.org/10.1016/j.stemcr.2015.07.010
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author Eberhardt, Esther
Havlicek, Steven
Schmidt, Diana
Link, Andrea S.
Neacsu, Cristian
Kohl, Zacharias
Hampl, Martin
Kist, Andreas M.
Klinger, Alexandra
Nau, Carla
Schüttler, Jürgen
Alzheimer, Christian
Winkler, Jürgen
Namer, Barbara
Winner, Beate
Lampert, Angelika
author_facet Eberhardt, Esther
Havlicek, Steven
Schmidt, Diana
Link, Andrea S.
Neacsu, Cristian
Kohl, Zacharias
Hampl, Martin
Kist, Andreas M.
Klinger, Alexandra
Nau, Carla
Schüttler, Jürgen
Alzheimer, Christian
Winkler, Jürgen
Namer, Barbara
Winner, Beate
Lampert, Angelika
author_sort Eberhardt, Esther
collection PubMed
description Human pluripotent stem cells (hPSCs) offer the opportunity to generate neuronal cells, including nociceptors. Using a chemical-based approach, we generated nociceptive sensory neurons from HUES6 embryonic stem cells and retrovirally reprogrammed induced hPSCs derived from fibroblasts. The nociceptive neurons expressed respective markers and showed tetrodotoxin-sensitive (TTXs) and -resistant (TTXr) voltage-gated sodium currents in patch-clamp experiments. In contrast to their counterparts from rodent dorsal root ganglia, TTXr currents of hPSC-derived nociceptors unexpectedly displayed a significantly more hyperpolarized voltage dependence of activation and fast inactivation. This apparent discrepancy is most likely due to a substantial expression of the developmentally important sodium channel NAV1.5. In view of the obstacles to recapitulate neuropathic pain in animal models, our data advance hPSC-derived nociceptors as a better model to study developmental and pathogenetic processes in human nociceptive neurons and to develop more specific small molecules to attenuate pain.
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spelling pubmed-46185922015-11-24 Pattern of Functional TTX-Resistant Sodium Channels Reveals a Developmental Stage of Human iPSC- and ESC-Derived Nociceptors Eberhardt, Esther Havlicek, Steven Schmidt, Diana Link, Andrea S. Neacsu, Cristian Kohl, Zacharias Hampl, Martin Kist, Andreas M. Klinger, Alexandra Nau, Carla Schüttler, Jürgen Alzheimer, Christian Winkler, Jürgen Namer, Barbara Winner, Beate Lampert, Angelika Stem Cell Reports Report Human pluripotent stem cells (hPSCs) offer the opportunity to generate neuronal cells, including nociceptors. Using a chemical-based approach, we generated nociceptive sensory neurons from HUES6 embryonic stem cells and retrovirally reprogrammed induced hPSCs derived from fibroblasts. The nociceptive neurons expressed respective markers and showed tetrodotoxin-sensitive (TTXs) and -resistant (TTXr) voltage-gated sodium currents in patch-clamp experiments. In contrast to their counterparts from rodent dorsal root ganglia, TTXr currents of hPSC-derived nociceptors unexpectedly displayed a significantly more hyperpolarized voltage dependence of activation and fast inactivation. This apparent discrepancy is most likely due to a substantial expression of the developmentally important sodium channel NAV1.5. In view of the obstacles to recapitulate neuropathic pain in animal models, our data advance hPSC-derived nociceptors as a better model to study developmental and pathogenetic processes in human nociceptive neurons and to develop more specific small molecules to attenuate pain. Elsevier 2015-08-28 /pmc/articles/PMC4618592/ /pubmed/26321143 http://dx.doi.org/10.1016/j.stemcr.2015.07.010 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Report
Eberhardt, Esther
Havlicek, Steven
Schmidt, Diana
Link, Andrea S.
Neacsu, Cristian
Kohl, Zacharias
Hampl, Martin
Kist, Andreas M.
Klinger, Alexandra
Nau, Carla
Schüttler, Jürgen
Alzheimer, Christian
Winkler, Jürgen
Namer, Barbara
Winner, Beate
Lampert, Angelika
Pattern of Functional TTX-Resistant Sodium Channels Reveals a Developmental Stage of Human iPSC- and ESC-Derived Nociceptors
title Pattern of Functional TTX-Resistant Sodium Channels Reveals a Developmental Stage of Human iPSC- and ESC-Derived Nociceptors
title_full Pattern of Functional TTX-Resistant Sodium Channels Reveals a Developmental Stage of Human iPSC- and ESC-Derived Nociceptors
title_fullStr Pattern of Functional TTX-Resistant Sodium Channels Reveals a Developmental Stage of Human iPSC- and ESC-Derived Nociceptors
title_full_unstemmed Pattern of Functional TTX-Resistant Sodium Channels Reveals a Developmental Stage of Human iPSC- and ESC-Derived Nociceptors
title_short Pattern of Functional TTX-Resistant Sodium Channels Reveals a Developmental Stage of Human iPSC- and ESC-Derived Nociceptors
title_sort pattern of functional ttx-resistant sodium channels reveals a developmental stage of human ipsc- and esc-derived nociceptors
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618592/
https://www.ncbi.nlm.nih.gov/pubmed/26321143
http://dx.doi.org/10.1016/j.stemcr.2015.07.010
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