Department of Ophthalmology, School of Medicine, Sapporo Medical University, Sapporo 060-8556, Japan.
Department of Cardiovascular, Renal and Metabolic Medicine, Sapporo Medical University, Sapporo 060-8556, Japan.
Int J Mol Sci. 2023 Jul 14;24(14):11459. doi: 10.3390/ijms241411459.
To establish an appropriate in vitro model for the local environment of cardiomyocytes, three-dimensional (3D) spheroids derived from H9c2 cardiomyoblasts were prepared, and their morphological, biophysical phase contrast and biochemical characteristics were evaluated. The 3D H9c2 spheroids were successfully obtained, the sizes of the spheroids decreased, and they became stiffer during 3-4 days. In contrast to the cell multiplication that occurs in conventional 2D planar cell cultures, the 3D H9c2 spheroids developed into a more mature form without any cell multiplication being detected. qPCR analyses of the 3D H9c2 spheroids indicated that the production of collagen4 (COL4) and fibronectin (FN), connexin43 (CX43), β-catenin, N-cadherin, STAT3, and HIF1 molecules had increased and that the production of COL6 and α-smooth muscle actin (α-SMA) molecules had decreased as compared to 2D cultured cells. In addition, treatment with rapamycin (Rapa), an mTOR complex (mTORC) 1 inhibitor, and Torin 1, an mTORC1/2 inhibitor, resulted in significantly decreased cell densities of the 2D cultured H9c2 cells, but the size and stiffness of the H9c2 cells within the 3D spheroids were reduced with the gene expressions of several of the above several factors being reduced. The metabolic responses to mTOR modulators were also different between the 2D and 3D cultures. These results suggest that as unique aspects of the local environments of the 3D spheroids, the spontaneous expression of GJ-related molecules and hypoxia within the core may be associated with their maturation, suggesting that this may become a useful in vitro model that replicates the local environment of cardiomyocytes.
为了建立心肌细胞局部环境的合适体外模型,制备了来源于 H9c2 心肌细胞的三维(3D)球体,并评估了其形态、生物物理相差和生化特性。成功获得了 3D H9c2 球体,球体大小在 3-4 天内减小,并且变得更硬。与传统的 2D 平面细胞培养中发生的细胞增殖不同,3D H9c2 球体发育成更成熟的形式,没有检测到任何细胞增殖。3D H9c2 球体的 qPCR 分析表明,胶原蛋白 4(COL4)和纤维连接蛋白(FN)、连接蛋白 43(CX43)、β-连环蛋白、N-钙黏蛋白、STAT3 和 HIF1 分子的产生增加,而 COL6 和α-平滑肌肌动蛋白(α-SMA)分子的产生减少与 2D 培养细胞相比。此外,雷帕霉素(Rapa),一种 mTOR 复合物(mTORC)1 抑制剂,和 Torin 1,一种 mTORC1/2 抑制剂,处理导致 2D 培养的 H9c2 细胞的细胞密度显著降低,但 3D 球体中 H9c2 细胞的大小和硬度降低,同时几种上述因素的基因表达降低。mTOR 调节剂的代谢反应在 2D 和 3D 培养物之间也不同。这些结果表明,作为 3D 球体局部环境的独特方面,核心内 GJ 相关分子的自发表达和缺氧可能与它们的成熟有关,这表明它可能成为一种有用的体外模型,可复制心肌细胞的局部环境。