Shimoide Takeshi, Kawao Naoyuki, Tamura Yukinori, Morita Hironobu, Kaji Hiroshi
Department of Physiology and Regenerative Medicine, Kindai University Faculty of Medicine, 377-2 Ohnohigashi, Osakasayama, Osaka 589-8511, Japan.
Department of Physiology, Gifu University Graduate School of Medicine, Gifu 501-1194, Japan.
Biochem Biophys Res Commun. 2016 Oct 21;479(3):602-606. doi: 10.1016/j.bbrc.2016.09.126. Epub 2016 Sep 25.
Skeletal muscle hypertrophy and wasting are induced by hypergravity and microgravity, respectively. However, the mechanisms by which gravity change regulates muscle mass still remain unclear. We previously reported that hypergravity increases muscle mass via the vestibular system in mice. In this study, we performed comparative DNA microarray analysis of the soleus muscle from mice kept in 1 or 3 g environments with or without vestibular lesions. Mice were kept in 1 g or 3 g environment for 4 weeks by using a centrifuge 14 days after surgical bilateral vestibular lesions. FKBP5 was extracted as a gene whose expression was enhanced by hypergravity through the vestibular system. Stable FKBP5 overexpression increased the phosphorylations of Akt and p70 S6 kinase (muscle protein synthesis pathway) and myosin heavy chain, a myotube gene, mRNA level in mouse myoblastic C2C12 cells, although it reduced the mRNA levels of atrogin-1 and MuRF1, muscle protein degradation-related genes. In conclusion, we first showed that FKBP5 is induced by hypergravity through the vestibular system in anti-gravity muscle of mice. Our data suggest that FKBP5 might increase muscle mass through the enhancements of muscle protein synthesis and myotube differentiation as well as an inhibition of muscle protein degradation in mice.
骨骼肌肥大和消瘦分别由超重力和微重力诱导。然而,重力变化调节肌肉质量的机制仍不清楚。我们之前报道过超重力通过小鼠的前庭系统增加肌肉质量。在本研究中,我们对饲养在1g或3g环境中有或无前庭损伤的小鼠比目鱼肌进行了比较DNA微阵列分析。在双侧前庭手术损伤14天后,使用离心机将小鼠置于1g或3g环境中4周。FKBP5被提取为一个其表达通过前庭系统被超重力增强的基因。稳定的FKBP5过表达增加了Akt和p70 S6激酶(肌肉蛋白合成途径)的磷酸化以及肌球蛋白重链(一种肌管基因)在小鼠成肌C2C12细胞中的mRNA水平,尽管它降低了atrogin-1和MuRF1(肌肉蛋白降解相关基因)的mRNA水平。总之,我们首次表明FKBP5在小鼠抗重力肌肉中通过前庭系统被超重力诱导。我们的数据表明FKBP5可能通过增强肌肉蛋白合成和肌管分化以及抑制小鼠肌肉蛋白降解来增加肌肉质量。