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Impact of TIEG1 on the structural properties of fast‐ and slow‐twitch skeletal muscle
Author(s) -
Kammoun Malek,
Meme Sandra,
Meme William,
Subramaniam Malayannan,
Hawse John R.,
Ca Francis,
Bensamoun Sabine F.
Publication year - 2017
Publication title -
muscle and nerve
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.025
H-Index - 145
eISSN - 1097-4598
pISSN - 0148-639X
DOI - 10.1002/mus.25252
Subject(s) - muscle hypertrophy , skeletal muscle , hyperplasia , chemistry , cancer research , microbiology and biotechnology , anatomy , biology , endocrinology
Transforming growth factor‐beta (TGF‐β)–inducible early gene‐1 (TIEG1) is a transcription factor that is highly expressed in skeletal muscle. The purpose of this study was to characterize the structural properties of both fast‐twitch (EDL) and slow‐twitch (soleus) muscles in the hindlimb of TIEG1‐deficient (TIEG1 −/− ) mice. Methods Ten slow and 10 fast muscles were analyzed from TIEG1 −/− and wild‐type (WT) mice using MRI texture (MRI‐TA) and histological analyses. Results MRI‐TA could discriminate between WT slow and fast muscles. Deletion of the TIEG1 gene led to changes in the texture profile within both muscle types. Specifically, muscle isolated from TIEG1 −/− mice displayed hypertrophy, hyperplasia, and a modification of fiber area distribution. Conclusions We demonstrated that TIEG1 plays an important role in the structural properties of skeletal muscle. This study further implicates important roles for TIEG1 in the development of skeletal muscle and suggests that defects in TIEG1 expression and/or function may be associated with muscle disease. Muscle Nerve 55 : 410–416, 2017