Dalmao-Fernandez Andrea, Aizenshtadt Aleksandra, Bakke Hege G, Krauss Stefan, Rustan Arild C, Thoresen G Hege, Kase Eili Tranheim
Section for Pharmacology and Pharmaceutical Biosciences, Department of Pharmacy, University of Oslo, Oslo, Norway.
Hybrid Technology Hub Centre of Excellence, Faculty of Medicine, University of Oslo, Oslo, Norway.
Front Bioeng Biotechnol. 2023 Mar 23;11:1130693. doi: 10.3389/fbioe.2023.1130693. eCollection 2023.
Skeletal muscle is a major contributor to whole-body energy homeostasis and the utilization of fatty acids and glucose. At present, 2D cell models have been the most used cellular models to study skeletal muscle energy metabolism. However, the transferability of the results to might be limited. This project aimed to develop and characterize a skeletal muscle 3D cell model (myospheres) as an easy and low-cost tool to study molecular mechanisms of energy metabolism. We demonstrated that human primary myoblasts form myospheres without external matrix support and carry structural and molecular characteristics of mature skeletal muscle after 10 days of differentiation. We found significant metabolic differences between the 2D myotubes model and myospheres. In particular, myospheres showed increased lipid oxidative metabolism than the 2D myotubes model, which oxidized relatively more glucose and accumulated more oleic acid. These analyses demonstrate model differences that can have an impact and should be taken into consideration for studying energy metabolism and metabolic disorders in skeletal muscle.
骨骼肌是全身能量稳态以及脂肪酸和葡萄糖利用的主要贡献者。目前,二维细胞模型一直是研究骨骼肌能量代谢最常用的细胞模型。然而,研究结果向[此处原文缺失相关内容]的可转移性可能有限。本项目旨在开发并表征一种骨骼肌三维细胞模型(肌球),作为一种研究能量代谢分子机制的简便且低成本的工具。我们证明,人类原代成肌细胞在无外部基质支持的情况下形成肌球,并且在分化10天后具有成熟骨骼肌的结构和分子特征。我们发现二维肌管模型和肌球之间存在显著的代谢差异。特别是,肌球比二维肌管模型显示出更高的脂质氧化代谢,二维肌管模型氧化相对更多的葡萄糖并积累更多的油酸。这些分析表明模型差异可能会产生影响,在研究骨骼肌的能量代谢和代谢紊乱时应予以考虑。