Graduate School of Pharmaceutical Sciences, Chiba University, 1-8-1 Inohana, Chuo-Ku, Chiba, Chiba, 260-8675, Japan.
Division of Pharmacy, Chiba University Hospital, 1-8-1 Inohana, Chuo-Ku, Chiba, Chiba, 260-8677, Japan.
In Vitro Cell Dev Biol Anim. 2023 Aug;59(7):505-513. doi: 10.1007/s11626-023-00788-w. Epub 2023 Jul 28.
Human vascular smooth muscle cells (SMCs) are adherent cells, and they cannot survive without scaffolds in suspension culture. Here, we aimed to establish a suspension culture of SMCs using the functional biopolymer FP003 and to investigate the proliferation status of the cells. When SMCs were suspension cultured with FP003, their proliferation was inhibited with a viability of 75% until day 15. When SMCs were re-plated on plastic plates after suspension culture with FP003 for 48 h, the SMCs proliferated as in a normal plate culture. The SMCs cultured in suspension with FP003 showed a relatively low phosphorylation of retinoblastoma protein, low expression of cyclin D1, high proportion of G0/G1 phase cells, low proportion of S phase cells, and no obvious signs of apoptosis, indicating that this culture system inhibited progression from the G1 to S phase. This growth arrest was a reversible property that showed no significant changes in the expressions of the marker proteins α-smooth muscle actin and smooth muscle myosin heavy chain. These results suggest that human SMCs can be stably cultured in suspension with FP003 without losing their characteristics when they are cultured on plastic plates again.
人血管平滑肌细胞(SMCs)是贴壁细胞,如果在悬浮培养中没有支架,它们就无法存活。在这里,我们旨在使用功能生物聚合物 FP003 建立 SMC 的悬浮培养,并研究细胞的增殖状态。当 SMC 用 FP003 进行悬浮培养时,它们的增殖受到抑制,直到第 15 天活力为 75%。当 SMC 在用 FP003 进行 48 小时悬浮培养后重新在塑料板上培养时,SMC 像在正常平板培养中一样增殖。用 FP003 悬浮培养的 SMC 中视网膜母细胞瘤蛋白的磷酸化程度相对较低,细胞周期蛋白 D1 的表达水平较低,G0/G1 期细胞比例较高,S 期细胞比例较低,没有明显的细胞凋亡迹象,表明该培养系统抑制了从 G1 期到 S 期的进展。这种生长停滞是一种可逆的特性,标志物蛋白α-平滑肌肌动蛋白和平滑肌肌球蛋白重链的表达没有明显变化。这些结果表明,人 SMC 可以在 FP003 中稳定地悬浮培养,当它们再次在塑料板上培养时,不会失去其特性。