Noninvasive Imaging of In Vivo MuRF1 Expression during Muscle Atrophy

被引:2
|
作者
Li, Wei [1 ]
Claypool, Mark D. [1 ]
Friera, Annabelle M. [1 ]
McLaughlin, John [1 ]
Baltgalvis, Kristen A. [1 ]
Smith, Ira J. [1 ]
Kinoshita, Taisei [1 ]
White, Kathy [1 ]
Lang, Wayne [1 ]
Godinez, Guillermo [1 ]
Payan, Donald G. [1 ]
Kinsella, Todd M. [1 ]
机构
[1] Rigel Pharmaceut Inc, Discovery Res, San Francisco, CA 94080 USA
来源
PLOS ONE | 2014年 / 9卷 / 04期
关键词
SKELETAL-MUSCLE; GLUCOCORTICOID-RECEPTOR; DISUSE; INVOLVE; DISEASE; MASS;
D O I
10.1371/journal.pone.0094032
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 39 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.
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收藏
页数:13
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