TY - JOUR
T1 - Nuclear factor E2-related factor 2 (NRF2) deficiency accelerates fast fibre type transition in soleus muscle during space flight
AU - Hayashi, Takuto
AU - Kudo, Takashi
AU - Fujita, Ryo
AU - Fujita, Shin ichiro
AU - Tsubouchi, Hirona
AU - Fuseya, Sayaka
AU - Suzuki, Riku
AU - Hamada, Michito
AU - Okada, Risa
AU - Muratani, Masafumi
AU - Shiba, Dai
AU - Suzuki, Takafumi
AU - Warabi, Eiji
AU - Yamamoto, Masayuki
AU - Takahashi, Satoru
N1 - Funding Information:
We would like to thank Ms Akane Yumoto of JAXA and Ms Hiromi Suzuki-Hashizume of the Japan Space Forum for coordinating the study, and Ms Naoko Murakami and Ms Rika Oshima of Advanced Engineering Services Co., Ltd for their assistance in animal care. This work was supported by a Grant-in-Aid for the Japan Aerospace Exploration Agency (14YPTK-005512; S.T.), Grant-in-Aid for Scientific Research on Innovative Areas from MEXT (18H04965; S.T.).
Publisher Copyright:
© 2021, The Author(s).
PY - 2021/12
Y1 - 2021/12
N2 - Microgravity induces skeletal muscle atrophy, particularly in the soleus muscle, which is predominantly composed of slow-twitch myofibre (type I) and is sensitive to disuse. Muscle atrophy is commonly known to be associated with increased production of reactive oxygen species. However, the role of NRF2, a master regulator of antioxidative response, in skeletal muscle plasticity during microgravity-induced atrophy, is not known. To investigate the role of NRF2 in skeletal muscle within a microgravity environment, wild-type and Nrf2-knockout (KO) mice were housed in the International Space Station for 31 days. Gene expression and histological analyses demonstrated that, under microgravity conditions, the transition of type I (oxidative) muscle fibres to type IIa (glycolytic) was accelerated in Nrf2-KO mice without affecting skeletal muscle mass. Therefore, our results suggest that NRF2 affects myofibre type transition during space flight.
AB - Microgravity induces skeletal muscle atrophy, particularly in the soleus muscle, which is predominantly composed of slow-twitch myofibre (type I) and is sensitive to disuse. Muscle atrophy is commonly known to be associated with increased production of reactive oxygen species. However, the role of NRF2, a master regulator of antioxidative response, in skeletal muscle plasticity during microgravity-induced atrophy, is not known. To investigate the role of NRF2 in skeletal muscle within a microgravity environment, wild-type and Nrf2-knockout (KO) mice were housed in the International Space Station for 31 days. Gene expression and histological analyses demonstrated that, under microgravity conditions, the transition of type I (oxidative) muscle fibres to type IIa (glycolytic) was accelerated in Nrf2-KO mice without affecting skeletal muscle mass. Therefore, our results suggest that NRF2 affects myofibre type transition during space flight.
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U2 - 10.1038/s42003-021-02334-4
DO - 10.1038/s42003-021-02334-4
M3 - Article
C2 - 34168270
AN - SCOPUS:85108802506
SN - 2399-3642
VL - 4
JO - Communications Biology
JF - Communications Biology
IS - 1
M1 - 787
ER -