Yang Bingquan, Liu Yuefei, Steinacker Jürgen Michael
Department of Endocrinology, Zhongda Hospital, Southeast University, Nanjing, China.
Division of Sports and Rehabilitation Medicine, Department of Cardiology, University of Ulm, Ulm, Germany.
Front Nutr. 2023 May 10;10:1145236. doi: 10.3389/fnut.2023.1145236. eCollection 2023.
Cellular adaptation to physical training and energy metabolism play an important role during physical exercise. This study sought to investigate the effects of α-KG on cell growth and energy metabolism in C2C12 cell culture.
C2C12 cells were cultured in media pretreated without (control) or with α-KG at different concentrations, and cells and media were harvested every 24 h for 8 days. From cell counts, specific cell growth rate (SGR) and doubling time were calculated. The content of glucose, glutamine, lactate, and ammonia in media was determined, and the specific consumption rate (SCR) or production rate (SPR) was calculated. Additionally, cell colony-forming efficiency (CFE) was determined.
The control cells showed a CFE at 50%, a typical cell growth curve in the first 5 days with a mean SGR at 0.86/day, and a mean cell count doubling time at 19.4 h. In the group with α-KG at 100 mM, the cells underwent rapid cell death, and thus no further analysis was made. The treatment with α-KG at lower concentrations (0.1 mM and 1.0 mM) led to a higher CFE at 68 and 55%, respectively, whereas those in groups with higher α-KG concentration decreased (10 and 6% for 20 mM and 30 mM α-KG, respectively). The mean SGR was 0.95/day, 0.94/day, 0.77/day, 0.71/day, and 0.65/day for groups treated with α-KG at 0.1, 1.0, 10.0, 20.0, and 30.0 mM, respectively, and the corresponding cell count doubling time was 17.6, 17.8, 20.9, 24.6, and 24.7 h, respectively. In comparison with that of the control group, the mean glucose SCR decreased in all the groups treated with α-KG, while the mean glutamine SCR remained unchanged; the mean lactate SPR increased in the groups treated with α-KG ≥ 20.0 mM. Finally, the mean SPR of ammonia was lower in all α-KG groups than that in the control.
The treatment with α-KG at lower concentrations increased cell growth whereas at higher concentrations decreased cell growth, and α-KG reduced glucose consumption and ammonia production. Therefore, α-KG stimulates cell growth in a dose-dependent manner, which is likely through the improvement of glucose and glutamine metabolism in a C2C12 culture setting.
细胞对体育锻炼的适应性和能量代谢在体育活动中起着重要作用。本研究旨在探讨α-酮戊二酸(α-KG)对C2C12细胞培养中细胞生长和能量代谢的影响。
将C2C12细胞培养在未预处理(对照)或含有不同浓度α-KG的培养基中,每24小时收集细胞和培养基,持续8天。通过细胞计数计算特定细胞生长率(SGR)和倍增时间。测定培养基中葡萄糖、谷氨酰胺、乳酸和氨的含量,并计算特定消耗率(SCR)或产生率(SPR)。此外,还测定了细胞集落形成效率(CFE)。
对照细胞的CFE为50%,在前5天呈现典型的细胞生长曲线,平均SGR为0.86/天,平均细胞计数倍增时间为19.4小时。在100 mM α-KG组中,细胞迅速死亡,因此未进行进一步分析。较低浓度(0.1 mM和1.0 mM)的α-KG处理分别导致CFE升高至68%和55%,而较高α-KG浓度组的CFE降低(20 mM和30 mM α-KG组分别为10%和6%)。α-KG处理组在0.1、1.0、10.0、20.0和30.0 mM时的平均SGR分别为0.95/天、0.94/天、0.77/天、0.71/天和0.65/天,相应的细胞计数倍增时间分别为17.6、17.8、20.9、24.6和24.7小时。与对照组相比,所有α-KG处理组的平均葡萄糖SCR均降低,而平均谷氨酰胺SCR保持不变;α-KG≥20.0 mM处理组的平均乳酸SPR升高。最后,所有α-KG组的氨平均SPR均低于对照组。
较低浓度的α-KG处理可促进细胞生长,而较高浓度则抑制细胞生长,且α-KG可降低葡萄糖消耗和氨产生。因此,α-KG以剂量依赖的方式刺激细胞生长,这可能是通过改善C2C12培养环境中的葡萄糖和谷氨酰胺代谢实现的。