Lee Ye-Eun, Jeong Eun Soo, Kim Young-Mog, Gong Seung Pyo
Department of Fisheries Biology, Pukyong National University, Busan, 48513 Korea.
Department of Food Science and Technology, Pukyong National University, Busan, 48513 Korea.
Cytotechnology. 2025 Feb;77(1):18. doi: 10.1007/s10616-024-00676-5. Epub 2024 Dec 12.
Culturing fish myogenic cells in vitro holds significant potential to revolutionize aquaculture practices and support sustainable food production. However, advancement in in vitro culture technologies for skeletal muscle-derived myogenic cells have predominantly focused on mammals, with limited studies on fish. Scaffold-based three-dimensional (3D) culture systems for fish myogenic cells remain underexplored, highlighting a critical research gap compared to mammalian systems. This study evaluated the effects of scaffold composition and manufacturing methods on cellular growth in the 3D culture of black sea bream () myogenic cells. Scaffolds were manufactured using three natural polymers: black sea bream-derived extracellular matrix (ECM), sodium alginate, and gelatin. Two scaffold types were tested: "cell-laden scaffolds" prepared by mixing cells into the pre-scaffold solution followed by gelation, and "cell-seeding scaffolds" produced by freezing, gelation, and lyophilization before cell inoculation. Scaffold characteristics, including pore size, porosity, swelling ratio, and degradation rate, were assessed. Cell-seeding scaffolds exhibited relatively larger pore size, higher porosity, and higher degradation rate, while cell-laden scaffolds had higher swelling ratios. When black sea bream myogenic cells were cultured in these scaffolds, cell-seeding scaffolds supported cellular growth, particularly when composed of 3% sodium alginate and 4% gelatin with any concentration of ECM. In contrast, cell-laden scaffolds did not support cellular growth regardless of their composition. These findings provide fundamental insights for optimizing scaffold properties to develop more optimized conditions for 3D culture of fish muscle lineage cells.
体外培养鱼类成肌细胞在彻底改变水产养殖实践和支持可持续粮食生产方面具有巨大潜力。然而,骨骼肌源性成肌细胞的体外培养技术进展主要集中在哺乳动物上,对鱼类的研究有限。用于鱼类成肌细胞的基于支架的三维(3D)培养系统仍未得到充分探索,与哺乳动物系统相比,这凸显了一个关键的研究空白。本研究评估了支架组成和制造方法对黑鲷成肌细胞3D培养中细胞生长的影响。使用三种天然聚合物制造支架:黑鲷来源的细胞外基质(ECM)、海藻酸钠和明胶。测试了两种类型的支架:“载细胞支架”,通过将细胞混入预支架溶液中然后凝胶化制备;“接种细胞支架”,在细胞接种前通过冷冻、凝胶化和冻干产生。评估了支架的特性,包括孔径、孔隙率、溶胀率和降解率。接种细胞支架表现出相对较大的孔径、较高的孔隙率和较高的降解率,而载细胞支架具有较高的溶胀率。当黑鲷成肌细胞在这些支架中培养时,接种细胞支架支持细胞生长,特别是当由3%海藻酸钠和4%明胶以及任何浓度的ECM组成时。相比之下,载细胞支架无论其组成如何都不支持细胞生长。这些发现为优化支架特性以开发更优化的鱼类肌肉谱系细胞3D培养条件提供了基本见解。