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Resistance exercise increases muscle protein synthesis and translation of eukaryotic initiation factor 2Bepsilon mRNA in a mammalian target of rapamycin-dependent manner.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 2005 Mar 04; Vol. 280 (9), pp. 7570-80. Date of Electronic Publication: 2004 Dec 10. - Publication Year :
- 2005
-
Abstract
- The contribution of mammalian target of rapamycin (mTOR) signaling to the resistance exercise-induced stimulation of skeletal muscle protein synthesis was assessed by administering rapamycin to Sprague-Dawley rats 2 h prior to a bout of resistance exercise. Animals were sacrificed 16 h postexercise, and gastrocnemius protein synthesis, mTOR signaling, and biomarkers of translation initiation were assessed. Exercise stimulated the rate of protein synthesis; however, this effect was prevented by pretreatment with rapamycin. The stimulation of protein synthesis was mediated by an increase in translation initiation, since exercise caused an increase in polysome aggregation that was abrogated by rapamycin administration. Taken together, the data suggest that the effect of rapamycin was not mediated by reduced phosphorylation of eukaryotic initiation factor 4E (eIF4E) binding protein 1 (BP1), because exercise did not cause a significant change in 4E-BP1(Thr-70) phosphorylation, 4E-BP1-eIF4E association, or eIF4F complex assembly concomitant with increased protein synthetic rates. Alternatively, there was a rapamycin-sensitive decrease in relative eIF2Bepsilon(Ser-535) phosphorylation that was explained by a significant increase in the expression of eIF2Bepsilon protein. The proportion of eIF2Bepsilon mRNA in polysomes was increased following exercise, an effect that was prevented by rapamycin treatment, suggesting that the increase in eIF2Bepsilon protein expression was mediated by an mTOR-dependent increase in translation of the mRNA encoding the protein. The increase in eIF2Bepsilon mRNA translation and protein abundance occurred independent of similar changes in other eIF2B subunits. These data suggest a novel link between mTOR signaling and eIF2Bepsilon mRNA translation that could contribute to the stimulation of protein synthesis following acute resistance exercise.
- Subjects :
- Animals
Blotting, Western
Carrier Proteins metabolism
Eukaryotic Initiation Factor-2B metabolism
Eukaryotic Initiation Factors metabolism
Glycogen Synthase Kinase 3 metabolism
Intracellular Signaling Peptides and Proteins
Male
Muscle, Skeletal pathology
Phosphoproteins metabolism
Phosphorylation
Physical Conditioning, Animal
Polyribosomes chemistry
RNA, Messenger metabolism
RNA, Ribosomal chemistry
Rats
Rats, Sprague-Dawley
Reverse Transcriptase Polymerase Chain Reaction
Ribosomal Protein S6 chemistry
Signal Transduction
Sirolimus pharmacology
TOR Serine-Threonine Kinases
Time Factors
p38 Mitogen-Activated Protein Kinases metabolism
Eukaryotic Initiation Factor-2B physiology
Muscle, Skeletal metabolism
Protein Biosynthesis
Protein Kinases metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9258
- Volume :
- 280
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 15591312
- Full Text :
- https://doi.org/10.1074/jbc.M413732200