Noninvasive imaging of in vivo MuRF1 expression during muscle atrophy.

Numerous human diseases can lead to atrophy of skeletal muscle, and loss of this tissue has been correlated with increased mortality and morbidity rates. Clinically addressing muscle atrophy remains an unmet medical need, and the development of preclinical tools to assist drug discovery and basic re...

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Main Authors: Wei Li, Mark D Claypool, Annabelle M Friera, John McLaughlin, Kristen A Baltgalvis, Ira J Smith, Taisei Kinoshita, Kathy White, Wayne Lang, Guillermo Godinez, Donald G Payan, Todd M Kinsella
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3977994?pdf=render
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spelling doaj-408c765604924646b1fef41e484a25ef2020-11-24T21:45:44ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0194e9403210.1371/journal.pone.0094032Noninvasive imaging of in vivo MuRF1 expression during muscle atrophy.Wei LiMark D ClaypoolAnnabelle M FrieraJohn McLaughlinKristen A BaltgalvisIra J SmithTaisei KinoshitaKathy WhiteWayne LangGuillermo GodinezDonald G PayanTodd M KinsellaNumerous human diseases can lead to atrophy of skeletal muscle, and loss of this tissue has been correlated with increased mortality and morbidity rates. Clinically addressing muscle atrophy remains an unmet medical need, and the development of preclinical tools to assist drug discovery and basic research in this effort is important for advancing this goal. In this report, we describe the development of a bioluminescent gene reporter rat, based on the zinc finger nuclease-targeted insertion of a bicistronic luciferase reporter into the 3' untranslated region of a muscle specific E3 ubiquitin ligase gene, MuRF1 (Trim63). In longitudinal studies, we noninvasively assess atrophy-related expression of this reporter in three distinct models of muscle loss (sciatic denervation, hindlimb unloading and dexamethasone-treatment) and show that these animals are capable of generating refined detail on in vivo MuRF1 expression with high temporal and anatomical resolution.http://europepmc.org/articles/PMC3977994?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Wei Li
Mark D Claypool
Annabelle M Friera
John McLaughlin
Kristen A Baltgalvis
Ira J Smith
Taisei Kinoshita
Kathy White
Wayne Lang
Guillermo Godinez
Donald G Payan
Todd M Kinsella
spellingShingle Wei Li
Mark D Claypool
Annabelle M Friera
John McLaughlin
Kristen A Baltgalvis
Ira J Smith
Taisei Kinoshita
Kathy White
Wayne Lang
Guillermo Godinez
Donald G Payan
Todd M Kinsella
Noninvasive imaging of in vivo MuRF1 expression during muscle atrophy.
PLoS ONE
author_facet Wei Li
Mark D Claypool
Annabelle M Friera
John McLaughlin
Kristen A Baltgalvis
Ira J Smith
Taisei Kinoshita
Kathy White
Wayne Lang
Guillermo Godinez
Donald G Payan
Todd M Kinsella
author_sort Wei Li
title Noninvasive imaging of in vivo MuRF1 expression during muscle atrophy.
title_short Noninvasive imaging of in vivo MuRF1 expression during muscle atrophy.
title_full Noninvasive imaging of in vivo MuRF1 expression during muscle atrophy.
title_fullStr Noninvasive imaging of in vivo MuRF1 expression during muscle atrophy.
title_full_unstemmed Noninvasive imaging of in vivo MuRF1 expression during muscle atrophy.
title_sort noninvasive imaging of in vivo murf1 expression during muscle atrophy.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Numerous human diseases can lead to atrophy of skeletal muscle, and loss of this tissue has been correlated with increased mortality and morbidity rates. Clinically addressing muscle atrophy remains an unmet medical need, and the development of preclinical tools to assist drug discovery and basic research in this effort is important for advancing this goal. In this report, we describe the development of a bioluminescent gene reporter rat, based on the zinc finger nuclease-targeted insertion of a bicistronic luciferase reporter into the 3' untranslated region of a muscle specific E3 ubiquitin ligase gene, MuRF1 (Trim63). In longitudinal studies, we noninvasively assess atrophy-related expression of this reporter in three distinct models of muscle loss (sciatic denervation, hindlimb unloading and dexamethasone-treatment) and show that these animals are capable of generating refined detail on in vivo MuRF1 expression with high temporal and anatomical resolution.
url http://europepmc.org/articles/PMC3977994?pdf=render
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