Skeletal muscle in MuRF1 null mice is not spared in low-gravity conditions, indicating atrophy proceeds by unique mechanisms in space

被引:44
作者
Cadena, Samuel M. [1 ]
Zhang, Yunyu [1 ]
Fang, Jian [1 ]
Brachat, Sophie [2 ]
Kuss, Pia [2 ]
Giorgetti, Elisa [2 ]
Stodieck, Louis S. [3 ]
Kneissel, Michaela [2 ]
Glass, David J. [1 ]
机构
[1] Novartis Inst Biomed Res, 181 Massachusetts Ave, Cambridge, MA 02139 USA
[2] Novartis Inst Biomed Res, Novartis Campus, CH-4056 Basel, Switzerland
[3] Univ Colorado, BioServe Space Technol, Dept Aerosp Engn Sci, Boulder, CO 80309 USA
关键词
MYOSIN HEAVY-CHAIN; UBIQUITIN LIGASES; CANCER CACHEXIA; EXPRESSION; PROTEIN;
D O I
10.1038/s41598-019-45821-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Microgravity exposure is associated with loss of muscle mass and strength. The E3 ubiquitin ligase MuRF1 plays an integral role in degrading the contractile apparatus of skeletal muscle; MuRF1 null (KO) mice have shown protection in ground-based models of muscle atrophy. In contrast, MuRF1 KO mice subjected to 21 days of microgravity on the International Space Station (ISS) were not protected from muscle atrophy. In a time course experiment microgravity-induced muscle loss on the ISS showed MuRF1 gene expression was not upregulated. A comparison of the soleus transcriptome profiles between spaceflight and a publicly available data set for hindlimb suspension, a claimed surrogate model of microgravity, showed only marginal commonalities between the models. These findings demonstrate spaceflight induced atrophy is unique, and that understanding of effects of space requires study situated beyond the Earth's mesosphere.
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页数:11
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