一项体外研究表明,培养基中胎牛血清和葡萄糖浓度的变化会影响胶质母细胞瘤细胞的生存能力,这是通过调节细胞周期和活性氧来证明的。

Journal of biological methods Pub Date : 2025-08-28 eCollection Date: 2025-01-01 DOI:10.14440/jbm2025.0016
Rimshia Naaz, Mahadevaswamy G Kuruburu, Zonunsiami Leihang, Venugopal R Bovilla, Rajalakshmi Rajashetty, Ramya C Madhusetty, Vijaya Y Vaagesh, SubbaRao V Madhunapantula
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引用次数: 0

摘要

背景:体外细胞培养对于阐明各种信号机制和筛选药物以评估其安全性和有效性至关重要。然而,细胞在培养基中的增殖和存活会受到培养基成分变化的显著影响。例如,葡萄糖和胎牛血清(FBS)浓度的变化会影响细胞活力。尽管如此,只有少数研究考察了培养基中不同FBS和葡萄糖浓度对细胞活力的影响。目的:探讨葡萄糖和FBS剥夺对胶质母细胞瘤细胞的作用机制和细胞效应。方法:系统评价FBS和葡萄糖剥夺对大鼠C6和人U-87 MG胶质母细胞瘤细胞系增殖和存活的影响。结果:葡萄糖剥夺(0 mg/dL)显著降低C6细胞的活力,适度降低U-87 mg细胞的活力,补充葡萄糖(100 mg/dL, 400 mg/dL)后部分恢复。值得注意的是,FBS剥夺(0%)的影响更为深远,在两种细胞系中都诱导了活性氧的积累和广泛的细胞死亡。FBS(1、2、4、6、8和10%)恢复细胞活力并降低氧化应激。此外,葡萄糖和FBS剥夺都改变了抗氧化酶的表达和线粒体功能。葡萄糖和FBS剥夺也会不同程度地影响蛋白激酶B的磷酸化,提示代谢应激诱导的信号调节。结论:这些发现强调了胶质母细胞瘤细胞对葡萄糖和FBS剥夺的不同反应,并强调了在设计胶质母细胞瘤细胞实验时标准化培养条件,特别是血清和葡萄糖水平的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Variations in the fetal bovine serum and glucose concentration in the culture medium impact the viability of glioblastoma cells as evidenced through the modulation of cell cycle and reactive oxygen species: An in vitro study.

Background: In vitro cell culture is essential for elucidating various signaling mechanisms and screening pharmacological agents to assess their safety and efficacy. However, cell proliferation and survival in culture can be significantly influenced by variations in the composition of the culture medium. For instance, variations in glucose and fetal bovine serum (FBS) concentrations can impact cell viability. Despite this, only a few studies have examined the impact of varied FBS and glucose concentrations in culture media on cell viability.

Objective: This study investigated the mechanisms and cellular effects of glucose and FBS deprivation in glioblastoma cell lines.

Methods: We systematically evaluated the impact of FBS and glucose deprivation on the proliferation and survival of rat C6 and human U-87 MG glioblastoma cell lines.

Results: Glucose deprivation (0 mg/dL) significantly reduced the viability of C6 cells and moderately lowered the viability of U-87 MG cells, with partial recovery upon glucose supplementation (100 mg/dL, 400 mg/dL). Notably, FBS deprivation (0%) exerted a more profound effect, inducing the accumulation of reactive oxygen species and extensive cell death in both cell lines. Restoration of FBS (1, 2, 4, 6, 8, and 10%) recovered cell viability and reduced oxidative stress. Furthermore, both glucose and FBS deprivation altered antioxidant enzyme expression and mitochondrial function. Glucose and FBS deprivation also differentially affected protein kinase B phosphorylation, suggesting metabolic stress-induced signaling modulation.

Conclusion: These findings highlight the differential responses of glioblastoma cells to glucose and FBS deprivation and underscore the importance of standardizing culture conditions, especially serum and glucose levels, when designing experiments involving glioblastoma cells.

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