Correlation between Ribosome Biogenesis and the Magnitude of Hypertrophy in Overloaded Skeletal Muscle

PLoS One. 2016 Jan 29;11(1):e0147284. doi: 10.1371/journal.pone.0147284. eCollection 2016.

Abstract

External loads applied to skeletal muscle cause increases in the protein translation rate, which leads to muscle hypertrophy. Although some studies have demonstrated that increases in the capacity and efficiency of translation are involved in this process, it remains unclear how these two factors are related to the magnitude of muscle hypertrophy. The present study aimed to clarify the roles played by the capacity and efficiency of translation in muscle hypertrophy. We used an improved synergist ablation in which the magnitude of compensatory hypertrophy could be controlled by partial removal of synergist muscles. Male rats were assigned to four groups in which the plantaris muscle was unilaterally subjected to weak (WK), moderate (MO), middle (MI), and strong (ST) overloading by four types of synergist ablation. Fourteen days after surgery, the weight of the plantaris muscle per body weight increased by 8%, 22%, 32% and 45%, in the WK, MO, MI and ST groups, respectively. Five days after surgery, 18+28S rRNA content (an indicator of translational capacity) increased with increasing overload, with increases of 1.8-fold (MO), 2.2-fold (MI), and 2.5-fold (ST), respectively, relative to non-overloaded muscle (NL) in the WK group. rRNA content showed a strong correlation with relative muscle weight measured 14 days after surgery (r = 0.98). The phosphorylated form of p70S6K (a positive regulator of translational efficiency) showed a marked increase in the MO group, but no further increase was observed with further increase in overload (increases of 22.6-fold (MO), 17.4-fold (MI), and 18.2-fold (ST), respectively, relative to NL in the WK group). These results indicate that increases in ribosome biogenesis at the early phase of overloading are strongly dependent on the amount of overloading, and may play an important role in increasing the translational capacity for further gain of muscular size.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Hypertrophy / genetics
  • Hypertrophy / metabolism*
  • Hypertrophy / physiopathology
  • Hypertrophy / surgery
  • Male
  • Muscle Proteins / biosynthesis*
  • Muscle Proteins / genetics
  • Muscle, Skeletal / metabolism*
  • Muscle, Skeletal / physiopathology
  • Muscle, Skeletal / surgery
  • Organelle Biogenesis
  • Phosphorylation
  • Protein Biosynthesis*
  • RNA, Ribosomal, 18S / biosynthesis
  • RNA, Ribosomal, 18S / genetics
  • RNA, Ribosomal, 28S / biosynthesis
  • RNA, Ribosomal, 28S / genetics
  • Rats
  • Rats, Wistar
  • Ribosomal Protein S6 Kinases, 70-kDa / biosynthesis*
  • Ribosomal Protein S6 Kinases, 70-kDa / genetics
  • Ribosomes / genetics
  • Ribosomes / metabolism*

Substances

  • Muscle Proteins
  • RNA, Ribosomal, 18S
  • RNA, Ribosomal, 28S
  • Ribosomal Protein S6 Kinases, 70-kDa

Grants and funding

This work was supported by JSPS KAKENHI Grant Number 15H03078.