Spaceflight alters expression of microRNA during T-cell activation
Millie Hughes-Fulford1, Tammy T Chang2, Emily M Martinez2
1*Hughes-Fulford Laboratory, Department of Medicine, Metabolism Division, San Francisco Department of Veterans Affairs Medical Center, San Francisco, California, USA; and Northern California Institute for Research and Education, Department of Medicine, and Department of Surgery, University of California, San Francisco, California, USA milliehf@gmail.com.
Summary
Spaceflight alters microRNA (miRNA) expression, impacting T-cell activation and immune function. This study reveals gravity
Area of Science:
- Space Biology
- Immunology
- Molecular Biology
Background:
- Altered immune function in astronauts poses a significant challenge for long-term space exploration.
- Previous studies noted immune changes during spaceflight, but the underlying molecular mechanisms remain unclear.
Purpose of the Study:
- To investigate the hypothesis that spaceflight induces changes in microRNA (miRNA) expression.
- To determine the role of gravity in regulating T-cell activation at the molecular level.
Main Methods:
- Human leukocytes were stimulated with mitogens aboard the International Space Station.
- MicroRNA expression was analyzed using quantitative real-time PCR.
- Global gene expression was assessed using microarray analysis.
Main Results:
- MicroRNA-21 (miR-21) was significantly upregulated during early T-cell activation under normal gravity.
- Gene expression was suppressed under microgravity, with 85 genes showing significant downregulation.
- Identified EGR3, FASLG, BTG2, SPRY2, and TAGAP as co-upregulated targets of miR-21.
Conclusions:
- Spaceflight regulates miRNA expression, representing the first report of such a phenomenon.
- Gravity influences T-cell activation through transcriptional promotion and noncoding RNA-mediated translational repression.
- T-cell activation may be self-limited by miR-21-mediated inhibition of target gene translation.
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