TY - JOUR
T1 - REDD1 induction regulates the skeletal muscle gene expression signature following acute aerobic exercise
AU - Gordon, Bradley S.
AU - Steiner, Jennifer L.
AU - Rossetti, Michael L.
AU - Qiao, Shuxi
AU - Ellisen, Leif W.
AU - Govindarajan, Subramaniam S.
AU - Eroshkin, Alexey M.
AU - Williamson, David L.
AU - Coen, Paul M.
N1 - Funding Information:
This work was supported by startup funds from the University of Central Florida and Florida State University (B. S. Gordon) as well as by National Institutes of Health Grants F32-AA-023422 to J. L. Steiner and RO1-CA-122589 to L. W. Ellisen.
Publisher Copyright:
© 2017 the American Physiological Society.
PY - 2017/12/6
Y1 - 2017/12/6
N2 - The metabolic stress placed on skeletal muscle by aerobic exercise promotes acute and long-term health benefits in part through changes in gene expression. However, the transducers that mediate altered gene expression signatures have not been completely elucidated. Regulated in development and DNA damage 1 (REDD1) is a stress-induced protein whose expression is transiently increased in skeletal muscle following acute aerobic exercise. However, the role of this induction remains unclear. Because REDD1 altered gene expression in other model systems, we sought to determine whether REDD1 induction following acute exercise altered the gene expression signature in muscle. To do this, wild-type and REDD1-null mice were randomized to remain sedentary or undergo a bout of acute treadmill exercise. Exercised mice recovered for 1, 3, or 6 h before euthanization. Acute exercise induced a transient increase in REDD1 protein expression within the plantaris only at 1 h postexercise, and the induction occurred in both cytosolic and nuclear fractions. At this time point, global changes in gene expression were surveyed using microarray. REDD1 induction was required for the exercise-induced change in expression of 24 genes. Validation by RT-PCR confirmed that the exercise-mediated changes in genes related to exercise capacity, muscle protein metabolism, neuromuscular junction remodeling, and Metformin action were negated in REDD1-null mice. Finally, the exercise-mediated induction of REDD1 was partially dependent upon glucocorticoid receptor activation.
AB - The metabolic stress placed on skeletal muscle by aerobic exercise promotes acute and long-term health benefits in part through changes in gene expression. However, the transducers that mediate altered gene expression signatures have not been completely elucidated. Regulated in development and DNA damage 1 (REDD1) is a stress-induced protein whose expression is transiently increased in skeletal muscle following acute aerobic exercise. However, the role of this induction remains unclear. Because REDD1 altered gene expression in other model systems, we sought to determine whether REDD1 induction following acute exercise altered the gene expression signature in muscle. To do this, wild-type and REDD1-null mice were randomized to remain sedentary or undergo a bout of acute treadmill exercise. Exercised mice recovered for 1, 3, or 6 h before euthanization. Acute exercise induced a transient increase in REDD1 protein expression within the plantaris only at 1 h postexercise, and the induction occurred in both cytosolic and nuclear fractions. At this time point, global changes in gene expression were surveyed using microarray. REDD1 induction was required for the exercise-induced change in expression of 24 genes. Validation by RT-PCR confirmed that the exercise-mediated changes in genes related to exercise capacity, muscle protein metabolism, neuromuscular junction remodeling, and Metformin action were negated in REDD1-null mice. Finally, the exercise-mediated induction of REDD1 was partially dependent upon glucocorticoid receptor activation.
UR - http://www.scopus.com/inward/record.url?scp=85037636145&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85037636145&partnerID=8YFLogxK
U2 - 10.1152/ajpendo.00120.2017
DO - 10.1152/ajpendo.00120.2017
M3 - Article
C2 - 28899858
AN - SCOPUS:85037636145
SN - 0193-1849
VL - 313
SP - E737-E747
JO - American Journal of Physiology - Endocrinology and Metabolism
JF - American Journal of Physiology - Endocrinology and Metabolism
IS - 6
ER -