Gravitational force modulates G2/M phase exit in mechanically unloaded myoblasts
Tatiana Benavides Damm1, Alfredo Franco-Obregón, Marcel Egli
1CC Aerospace Biomedical Science & Technology; Space Biology Group; University of Applied Sciences and Arts; Hergiswil, Switzerland; Institute for Biomechanics; Eidgenössische Technische Hochschule Zürich; Zürich, Switzerland.
Spaceflight causes muscle atrophy by slowing cell growth. Simulated microgravity delayed cell cycle progression, but hypergravity did not, suggesting distinct cellular responses to mechanical unloading and loading.
Area of Science:
- Cell Biology
- Space Medicine
- Skeletal Muscle Physiology
Background:
- Prolonged spaceflight leads to muscle mass loss and reduced strength, known as space atrophy.
- Microgravity causes mechanical unloading of skeletal muscle myoblasts, impairing cell proliferation and altering protein expression.
Purpose of the Study:
- To investigate the mechanisms behind muscle mass decline during microgravity exposure.
- To analyze the effects of simulated microgravity on C2C12 mouse muscle cell proliferation, cell cycle, and cyclin expression.
Main Methods:
- Culturing C2C12 mouse muscle cells under simulated microgravity (SM) and hypergravity (HG).
- Analyzing cell proliferation, cell cycle progression, and expression of cyclin B and D.
Main Results:
- Simulated microgravity (SM) significantly retarded cell growth and delayed G2/M phase progression by approximately 16 hours.
- Cells accumulated between the G2 checkpoint and anaphase onset in SM, with positive cyclin B expression.
- Hypergravity (HG) conditions did not affect proliferation or cell cycle progression, similar to 1g controls.
Conclusions:
- Simulated microgravity and hypergravity induce distinct cellular responses in cell cycle progression.
- The negative effects of microgravity on cell cycle progression can be reversed by normal terrestrial gravity.
- Cellular mechanotransduction pathways respond differently to mechanical unloading versus loading.
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