Alizadeh Sardroud Hamed, Shokhrollahi Barough Mahdieh, Askari Esfandyar, Akbari Mohsen
Laboratory for Innovations in Micro Engineering (LiME), Department of Mechanical Engineering, University of Victoria, Victoria, BC, Canada.
Terasaki Institute for Biomedical Innovations, Los Angeles, CA, USA.
NPJ Sci Food. 2025 Jul 25;9(1):153. doi: 10.1038/s41538-025-00498-5.
This study explores the feasibility of microcarrier-seeded muscle cell expansion and differentiation in simulated microgravity (µG) conditions, aiming to develop a proof-of-concept for producing cultivated meat in space. Gelatin microcarriers supported C2C12 expansion and myogenesis in static culture. The microcarriers were cultured in 1G (stirred bioreactor) and simulated µG bioreactors. µG slowed down the cell expansion, while the 1G condition showed a significant increase in cell expansion. Cells exhibited nuclear elongation and extended cell bodies over 7 days in both 1G and µG conditions. Flow cytometry and real-time polymerase chain reaction (RT-PCR) revealed enhanced myogenesis in both 1G and µG, though differentiation was delayed and gene expression significantly lower under µG. These results suggest that while µG initiates differentiation, the process is primarily limited to early stages. Despite the slower myogenesis, it remains feasible, and future research should focus on culture conditions to enhance muscle cell functionality in µG.
本研究探讨了在模拟微重力(µG)条件下微载体接种的肌肉细胞扩增和分化的可行性,旨在为在太空中生产培养肉建立一个概念验证。明胶微载体在静态培养中支持C2C12细胞的扩增和肌生成。将微载体分别在1G(搅拌生物反应器)和模拟µG生物反应器中培养。µG减缓了细胞扩增,而1G条件下细胞扩增显著增加。在1G和µG条件下,细胞在7天内均表现出细胞核伸长和细胞体延长。流式细胞术和实时聚合酶链反应(RT-PCR)显示,1G和µG条件下肌生成均增强,尽管µG条件下分化延迟且基因表达显著降低。这些结果表明,虽然µG启动了分化,但该过程主要限于早期阶段。尽管肌生成较慢,但仍然可行,未来的研究应聚焦于改善培养条件,以增强µG条件下肌肉细胞的功能。