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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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 |
work_keys_str_mv |
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