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The cytokine receptor CRLF3 is a human neuroprotective EV-3 (Epo) receptor

The evolutionary conserved orphan cytokine receptor-like factor 3 (CRLF3) has been implicated in human disease, vertebrate hematopoiesis and insect neuroprotection. While its specific functions are elusive, experimental evidence points toward a general role in cell homeostasis. Erythropoietin (Epo)...

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Autores principales: Knorr, Debbra Y., Rodriguez Polo, Ignacio, Pies, Hanna S., Schwedhelm-Domeyer, Nicola, Pauls, Stephanie, Behr, Rüdiger, Heinrich, Ralf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10165946/
https://www.ncbi.nlm.nih.gov/pubmed/37168680
http://dx.doi.org/10.3389/fnmol.2023.1154509
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author Knorr, Debbra Y.
Rodriguez Polo, Ignacio
Pies, Hanna S.
Schwedhelm-Domeyer, Nicola
Pauls, Stephanie
Behr, Rüdiger
Heinrich, Ralf
author_facet Knorr, Debbra Y.
Rodriguez Polo, Ignacio
Pies, Hanna S.
Schwedhelm-Domeyer, Nicola
Pauls, Stephanie
Behr, Rüdiger
Heinrich, Ralf
author_sort Knorr, Debbra Y.
collection PubMed
description The evolutionary conserved orphan cytokine receptor-like factor 3 (CRLF3) has been implicated in human disease, vertebrate hematopoiesis and insect neuroprotection. While its specific functions are elusive, experimental evidence points toward a general role in cell homeostasis. Erythropoietin (Epo) is a major regulator of vertebrate hematopoiesis and a general cytoprotective cytokine. Erythropoietic functions mediated by classical Epo receptor are understood in great detail whereas Epo-mediated cytoprotective mechanisms are more complex due to involvement of additional Epo receptors and a non-erythropoietic splice variant with selectivity for certain receptors. In the present study, we show that the human CRLF3 mediates neuroprotection upon activation with the natural Epo splice variant EV-3. We generated CRLF3 knock-out iPSC lines and differentiated them toward the neuronal lineage. While apoptotic death of rotenone-challenged wild type iPSC-derived neurons was prevented by EV-3, EV-3-mediated neuroprotection was absent in CRLF3 knock-out neurons. Rotenone-induced apoptosis and EV-3-mediated neuroprotection were associated with differential expression of pro-and anti-apoptotic genes. Our data characterize human CRLF3 as a receptor involved in Epo-mediated neuroprotection and identify CRLF3 as the first known receptor for EV-3.
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spelling pubmed-101659462023-05-09 The cytokine receptor CRLF3 is a human neuroprotective EV-3 (Epo) receptor Knorr, Debbra Y. Rodriguez Polo, Ignacio Pies, Hanna S. Schwedhelm-Domeyer, Nicola Pauls, Stephanie Behr, Rüdiger Heinrich, Ralf Front Mol Neurosci Molecular Neuroscience The evolutionary conserved orphan cytokine receptor-like factor 3 (CRLF3) has been implicated in human disease, vertebrate hematopoiesis and insect neuroprotection. While its specific functions are elusive, experimental evidence points toward a general role in cell homeostasis. Erythropoietin (Epo) is a major regulator of vertebrate hematopoiesis and a general cytoprotective cytokine. Erythropoietic functions mediated by classical Epo receptor are understood in great detail whereas Epo-mediated cytoprotective mechanisms are more complex due to involvement of additional Epo receptors and a non-erythropoietic splice variant with selectivity for certain receptors. In the present study, we show that the human CRLF3 mediates neuroprotection upon activation with the natural Epo splice variant EV-3. We generated CRLF3 knock-out iPSC lines and differentiated them toward the neuronal lineage. While apoptotic death of rotenone-challenged wild type iPSC-derived neurons was prevented by EV-3, EV-3-mediated neuroprotection was absent in CRLF3 knock-out neurons. Rotenone-induced apoptosis and EV-3-mediated neuroprotection were associated with differential expression of pro-and anti-apoptotic genes. Our data characterize human CRLF3 as a receptor involved in Epo-mediated neuroprotection and identify CRLF3 as the first known receptor for EV-3. Frontiers Media S.A. 2023-04-06 /pmc/articles/PMC10165946/ /pubmed/37168680 http://dx.doi.org/10.3389/fnmol.2023.1154509 Text en Copyright © 2023 Knorr, Rodriguez Polo, Pies, Schwedhelm-Domeyer, Pauls, Behr and Heinrich. 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 Molecular Neuroscience
Knorr, Debbra Y.
Rodriguez Polo, Ignacio
Pies, Hanna S.
Schwedhelm-Domeyer, Nicola
Pauls, Stephanie
Behr, Rüdiger
Heinrich, Ralf
The cytokine receptor CRLF3 is a human neuroprotective EV-3 (Epo) receptor
title The cytokine receptor CRLF3 is a human neuroprotective EV-3 (Epo) receptor
title_full The cytokine receptor CRLF3 is a human neuroprotective EV-3 (Epo) receptor
title_fullStr The cytokine receptor CRLF3 is a human neuroprotective EV-3 (Epo) receptor
title_full_unstemmed The cytokine receptor CRLF3 is a human neuroprotective EV-3 (Epo) receptor
title_short The cytokine receptor CRLF3 is a human neuroprotective EV-3 (Epo) receptor
title_sort cytokine receptor crlf3 is a human neuroprotective ev-3 (epo) receptor
topic Molecular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10165946/
https://www.ncbi.nlm.nih.gov/pubmed/37168680
http://dx.doi.org/10.3389/fnmol.2023.1154509
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