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Irisin and FNDC5 in retrospect: An exercise hormone or a transmembrane receptor?

FNDC5 (fibronectin domain-containing [protein] 5) was initially discovered and characterized by two groups in 2002. In 2011 FNDC5 burst into prominence as the parent of irisin, a small protein containing the fibronectin type III domain. Irisin was proposed to be secreted by skeletal muscle cells in...

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Autor principal: Erickson, Harold P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3774709/
https://www.ncbi.nlm.nih.gov/pubmed/24052909
http://dx.doi.org/10.4161/adip.26082
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author Erickson, Harold P
author_facet Erickson, Harold P
author_sort Erickson, Harold P
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description FNDC5 (fibronectin domain-containing [protein] 5) was initially discovered and characterized by two groups in 2002. In 2011 FNDC5 burst into prominence as the parent of irisin, a small protein containing the fibronectin type III domain. Irisin was proposed to be secreted by skeletal muscle cells in response to exercise, and to circulate to fat tissue where it induced a transition to brown fat. Since brown fat results in dissipation of energy, this pathway is of considerable interest for metabolism and obesity. Here I review the original discoveries of FNDC5 and the more recent discovery of irisin. I note in particular three problems in the characterization of irisin: the antibodies used to detect irisin in plasma lack validity; the recombinant protein used to demonstrate activity in cell culture was severely truncated; and the degree of shedding of soluble irisin from the cell surface has not been quantitated. The original discovery proposing that FNDC5 may be a transmembrane receptor may deserve a new look.
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spelling pubmed-37747092013-09-19 Irisin and FNDC5 in retrospect: An exercise hormone or a transmembrane receptor? Erickson, Harold P Adipocyte Commentary FNDC5 (fibronectin domain-containing [protein] 5) was initially discovered and characterized by two groups in 2002. In 2011 FNDC5 burst into prominence as the parent of irisin, a small protein containing the fibronectin type III domain. Irisin was proposed to be secreted by skeletal muscle cells in response to exercise, and to circulate to fat tissue where it induced a transition to brown fat. Since brown fat results in dissipation of energy, this pathway is of considerable interest for metabolism and obesity. Here I review the original discoveries of FNDC5 and the more recent discovery of irisin. I note in particular three problems in the characterization of irisin: the antibodies used to detect irisin in plasma lack validity; the recombinant protein used to demonstrate activity in cell culture was severely truncated; and the degree of shedding of soluble irisin from the cell surface has not been quantitated. The original discovery proposing that FNDC5 may be a transmembrane receptor may deserve a new look. Landes Bioscience 2013-10-01 2013-08-19 /pmc/articles/PMC3774709/ /pubmed/24052909 http://dx.doi.org/10.4161/adip.26082 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Commentary
Erickson, Harold P
Irisin and FNDC5 in retrospect: An exercise hormone or a transmembrane receptor?
title Irisin and FNDC5 in retrospect: An exercise hormone or a transmembrane receptor?
title_full Irisin and FNDC5 in retrospect: An exercise hormone or a transmembrane receptor?
title_fullStr Irisin and FNDC5 in retrospect: An exercise hormone or a transmembrane receptor?
title_full_unstemmed Irisin and FNDC5 in retrospect: An exercise hormone or a transmembrane receptor?
title_short Irisin and FNDC5 in retrospect: An exercise hormone or a transmembrane receptor?
title_sort irisin and fndc5 in retrospect: an exercise hormone or a transmembrane receptor?
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3774709/
https://www.ncbi.nlm.nih.gov/pubmed/24052909
http://dx.doi.org/10.4161/adip.26082
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