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Irisin – a myth rather than an exercise-inducible myokine
The myokine irisin is supposed to be cleaved from a transmembrane precursor, FNDC5 (fibronectin type III domain containing 5), and to mediate beneficial effects of exercise on human metabolism. However, evidence for irisin circulating in blood is largely based on commercial ELISA kits which are base...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352853/ https://www.ncbi.nlm.nih.gov/pubmed/25749243 http://dx.doi.org/10.1038/srep08889 |
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author | Albrecht, Elke Norheim, Frode Thiede, Bernd Holen, Torgeir Ohashi, Tomoo Schering, Lisa Lee, Sindre Brenmoehl, Julia Thomas, Selina Drevon, Christian A. Erickson, Harold P. Maak, Steffen |
author_facet | Albrecht, Elke Norheim, Frode Thiede, Bernd Holen, Torgeir Ohashi, Tomoo Schering, Lisa Lee, Sindre Brenmoehl, Julia Thomas, Selina Drevon, Christian A. Erickson, Harold P. Maak, Steffen |
author_sort | Albrecht, Elke |
collection | PubMed |
description | The myokine irisin is supposed to be cleaved from a transmembrane precursor, FNDC5 (fibronectin type III domain containing 5), and to mediate beneficial effects of exercise on human metabolism. However, evidence for irisin circulating in blood is largely based on commercial ELISA kits which are based on polyclonal antibodies (pAbs) not previously tested for cross-reacting serum proteins. We have analyzed four commercial pAbs by Western blotting, which revealed prominent cross-reactivity with non-specific proteins in human and animal sera. Using recombinant glycosylated and non-glycosylated irisin as positive controls, we found no immune-reactive bands of the expected size in any biological samples. A FNDC5 signature was identified at ~20 kDa by mass spectrometry in human serum but was not detected by the commercial pAbs tested. Our results call into question all previous data obtained with commercial ELISA kits for irisin, and provide evidence against a physiological role for irisin in humans and other species. |
format | Online Article Text |
id | pubmed-4352853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43528532015-03-17 Irisin – a myth rather than an exercise-inducible myokine Albrecht, Elke Norheim, Frode Thiede, Bernd Holen, Torgeir Ohashi, Tomoo Schering, Lisa Lee, Sindre Brenmoehl, Julia Thomas, Selina Drevon, Christian A. Erickson, Harold P. Maak, Steffen Sci Rep Article The myokine irisin is supposed to be cleaved from a transmembrane precursor, FNDC5 (fibronectin type III domain containing 5), and to mediate beneficial effects of exercise on human metabolism. However, evidence for irisin circulating in blood is largely based on commercial ELISA kits which are based on polyclonal antibodies (pAbs) not previously tested for cross-reacting serum proteins. We have analyzed four commercial pAbs by Western blotting, which revealed prominent cross-reactivity with non-specific proteins in human and animal sera. Using recombinant glycosylated and non-glycosylated irisin as positive controls, we found no immune-reactive bands of the expected size in any biological samples. A FNDC5 signature was identified at ~20 kDa by mass spectrometry in human serum but was not detected by the commercial pAbs tested. Our results call into question all previous data obtained with commercial ELISA kits for irisin, and provide evidence against a physiological role for irisin in humans and other species. Nature Publishing Group 2015-03-09 /pmc/articles/PMC4352853/ /pubmed/25749243 http://dx.doi.org/10.1038/srep08889 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Albrecht, Elke Norheim, Frode Thiede, Bernd Holen, Torgeir Ohashi, Tomoo Schering, Lisa Lee, Sindre Brenmoehl, Julia Thomas, Selina Drevon, Christian A. Erickson, Harold P. Maak, Steffen Irisin – a myth rather than an exercise-inducible myokine |
title | Irisin – a myth rather than an exercise-inducible myokine |
title_full | Irisin – a myth rather than an exercise-inducible myokine |
title_fullStr | Irisin – a myth rather than an exercise-inducible myokine |
title_full_unstemmed | Irisin – a myth rather than an exercise-inducible myokine |
title_short | Irisin – a myth rather than an exercise-inducible myokine |
title_sort | irisin – a myth rather than an exercise-inducible myokine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352853/ https://www.ncbi.nlm.nih.gov/pubmed/25749243 http://dx.doi.org/10.1038/srep08889 |
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