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NOCICEPTRA: Gene and microRNA Signatures and Their Trajectories Characterizing Human iPSC‐Derived Nociceptor Maturation

Nociceptors are primary afferent neurons serving the reception of acute pain but also the transit into maladaptive pain disorders. Since native human nociceptors are hardly available for mechanistic functional research, and rodent models do not necessarily mirror human pathologies in all aspects, hu...

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Autores principales: Zeidler, Maximilian, Kummer, Kai K., Schöpf, Clemens L., Kalpachidou, Theodora, Kern, Georg, Cader, M. Zameel, Kress, Michaela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8564443/
https://www.ncbi.nlm.nih.gov/pubmed/34486248
http://dx.doi.org/10.1002/advs.202102354
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author Zeidler, Maximilian
Kummer, Kai K.
Schöpf, Clemens L.
Kalpachidou, Theodora
Kern, Georg
Cader, M. Zameel
Kress, Michaela
author_facet Zeidler, Maximilian
Kummer, Kai K.
Schöpf, Clemens L.
Kalpachidou, Theodora
Kern, Georg
Cader, M. Zameel
Kress, Michaela
author_sort Zeidler, Maximilian
collection PubMed
description Nociceptors are primary afferent neurons serving the reception of acute pain but also the transit into maladaptive pain disorders. Since native human nociceptors are hardly available for mechanistic functional research, and rodent models do not necessarily mirror human pathologies in all aspects, human induced pluripotent stem cell‐derived nociceptors (iDN) offer superior advantages as a human model system. Unbiased mRNA::microRNA co‐sequencing, immunofluorescence staining, and qPCR validations, reveal expression trajectories as well as miRNA target spaces throughout the transition of pluripotent cells into iDNs. mRNA and miRNA candidates emerge as regulatory hubs for neurite outgrowth, synapse development, and ion channel expression. The exploratory data analysis tool NOCICEPTRA is provided as a containerized platform to retrieve experimentally determined expression trajectories, and to query custom gene sets for pathway and disease enrichments. Querying NOCICEPTRA for marker genes of cortical neurogenesis reveals distinct similarities and differences for cortical and peripheral neurons. The platform provides a public domain neuroresource to exploit the entire data sets and explore miRNA and mRNA as hubs regulating human nociceptor differentiation and function.
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spelling pubmed-85644432021-11-09 NOCICEPTRA: Gene and microRNA Signatures and Their Trajectories Characterizing Human iPSC‐Derived Nociceptor Maturation Zeidler, Maximilian Kummer, Kai K. Schöpf, Clemens L. Kalpachidou, Theodora Kern, Georg Cader, M. Zameel Kress, Michaela Adv Sci (Weinh) Research Articles Nociceptors are primary afferent neurons serving the reception of acute pain but also the transit into maladaptive pain disorders. Since native human nociceptors are hardly available for mechanistic functional research, and rodent models do not necessarily mirror human pathologies in all aspects, human induced pluripotent stem cell‐derived nociceptors (iDN) offer superior advantages as a human model system. Unbiased mRNA::microRNA co‐sequencing, immunofluorescence staining, and qPCR validations, reveal expression trajectories as well as miRNA target spaces throughout the transition of pluripotent cells into iDNs. mRNA and miRNA candidates emerge as regulatory hubs for neurite outgrowth, synapse development, and ion channel expression. The exploratory data analysis tool NOCICEPTRA is provided as a containerized platform to retrieve experimentally determined expression trajectories, and to query custom gene sets for pathway and disease enrichments. Querying NOCICEPTRA for marker genes of cortical neurogenesis reveals distinct similarities and differences for cortical and peripheral neurons. The platform provides a public domain neuroresource to exploit the entire data sets and explore miRNA and mRNA as hubs regulating human nociceptor differentiation and function. John Wiley and Sons Inc. 2021-09-05 /pmc/articles/PMC8564443/ /pubmed/34486248 http://dx.doi.org/10.1002/advs.202102354 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zeidler, Maximilian
Kummer, Kai K.
Schöpf, Clemens L.
Kalpachidou, Theodora
Kern, Georg
Cader, M. Zameel
Kress, Michaela
NOCICEPTRA: Gene and microRNA Signatures and Their Trajectories Characterizing Human iPSC‐Derived Nociceptor Maturation
title NOCICEPTRA: Gene and microRNA Signatures and Their Trajectories Characterizing Human iPSC‐Derived Nociceptor Maturation
title_full NOCICEPTRA: Gene and microRNA Signatures and Their Trajectories Characterizing Human iPSC‐Derived Nociceptor Maturation
title_fullStr NOCICEPTRA: Gene and microRNA Signatures and Their Trajectories Characterizing Human iPSC‐Derived Nociceptor Maturation
title_full_unstemmed NOCICEPTRA: Gene and microRNA Signatures and Their Trajectories Characterizing Human iPSC‐Derived Nociceptor Maturation
title_short NOCICEPTRA: Gene and microRNA Signatures and Their Trajectories Characterizing Human iPSC‐Derived Nociceptor Maturation
title_sort nociceptra: gene and microrna signatures and their trajectories characterizing human ipsc‐derived nociceptor maturation
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8564443/
https://www.ncbi.nlm.nih.gov/pubmed/34486248
http://dx.doi.org/10.1002/advs.202102354
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