4.7 Article

Ckip-1 3′-UTR Attenuates Simulated Microgravity-Induced Cardiac Atrophy

期刊

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2021.796902

关键词

Ckip-1 3 '-UTR; simulated microgravity; cardiac atrophy; lipid accumulation; CaMKK2

资金

  1. National Natural Science Foundation of China [81822026, 81701859, 31670865, 81830061, 31800708]
  2. Space Medical Experiment Project of China Manned Space Program [HYZHXM01007]
  3. Grant of State Key Lab of Space Medicine Fundamentals and Application [SMFA19A02, SMFA17B05]

向作者/读者索取更多资源

Microgravity has a significant impact on cardiovascular health, leading to damage and mass loss in the heart. The role of Ckip-1 in atrophic heart growth after simulated microgravity involves inhibiting lipid accumulation and activating gene expression related to fatty acid oxidation. This study highlights the potential of Ckip-1 as an important regulator in maintaining cardiac function in space environments.
Microgravity prominently affected cardiovascular health, which was the gravity-dependent physical factor. Deep space exploration had been increasing in frequency, but heart function was susceptible to conspicuous damage and cardiac mass declined in weightlessness. Understanding of the etiology of cardiac atrophy exposed to microgravity currently remains limited. The 3 & PRIME;-untranslated region (UTR) of casein kinase-2 interacting protein-1 (Ckip-1) was a pivotal mediator in pressure overload-induced cardiac remodeling. However, the role of Ckip-1 3 & PRIME;-UTR in the heart during microgravity was unknown. We analyzed Ckip-1 mRNA 3 & PRIME;-UTR and coding sequence (CDS) expression levels in ground-based analogs such as mice hindlimb unloading (HU) and rhesus monkey head-down bed rest model. Ckip-1 3 & PRIME;-UTR had transcribed levels in the opposite change trend with cognate CDS expression in the hearts. We then subjected wild-type (WT) mice and cardiac-specific Ckip-1 3 & PRIME;-UTR-overexpressing mice to hindlimb unloading for 28 days. Our results uncovered that Ckip-1 3 & PRIME;-UTR remarkably attenuated cardiac dysfunction and mass loss in simulated microgravity environments. Mechanistically, Ckip-1 3 & PRIME;-UTR inhibited lipid accumulation and elevated fatty acid oxidation-related gene expression in the hearts through targeting calcium/calmodulin-dependent kinase 2 (CaMKK2) and activation of the AMPK-PPAR alpha-CPT1b signaling pathway. These findings demonstrated Ckip-1 3 & PRIME;-UTR was an important regulator in atrophic heart growth after simulated microgravity.

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