Sun Li-Yi, Pang Cheng-Yoong, Li Dian-Kun, Liao Chia-Hsin, Huang Wei-Chao, Wu Chao-Chuan, Chou Yi-Yo, Li Wei Wu, Chen Shin-Yuan, Liu Hwan-Wun, Chang Yao-Jen, Cheng Ching-Feng
J Biomed Sci. 2013 Aug 1;20(1):53. doi: 10.1186/1423-0127-20-53.
Antioxidants have been shown to enhance the proliferation of adipose-derived mesenchymal stem cells (ADMSCs) in vitro, although the detailed mechanism(s) and potential side effects are not fully understood.
During log-phase growth, exposure to ImF-A resulted in a higher percentage of ADMSCs in the S phase of the cell cycle and a smaller percentage in G0/G1 phase. This resulted in a significantly reduced cell-doubling time and increased number of cells in the antioxidant-supplemented cultures compared with those supplemented with FGF-2 alone, an approximately 225% higher cell density after 7 days. Western blotting showed that the levels of the CDK inhibitors p21 and p27 decreased after ImF-A treatment, whereas CDK2, CDK4, and CDC2 levels clearly increased. In addition, ImF-A resulted in significant reduction in the expression of CD29, CD90, and CD105, whereas relative telomere length, osteogenesis, adipogenesis, and chondrogenesis were enhanced. The results were similar for ADMSCs treated with antioxidants and those under hypoxic conditions.
Antioxidant treatment promotes entry of ADMSCs into the S phase by suppressing cyclin-dependent kinase inhibitors and results in rapid cell proliferation similar to that observed under hypoxic conditions.
抗氧化剂已被证明可在体外增强脂肪来源间充质干细胞(ADMSCs)的增殖,尽管其详细机制和潜在副作用尚未完全明确。
在对数生长期,暴露于ImF-A导致处于细胞周期S期的ADMSCs百分比更高,而处于G0/G1期的百分比更低。这导致细胞倍增时间显著缩短,与仅添加FGF-2的培养物相比,抗氧化剂补充培养物中的细胞数量增加,7天后细胞密度高出约225%。蛋白质印迹显示,ImF-A处理后CDK抑制剂p21和p27的水平降低,而CDK2、CDK4和CDC2的水平明显升高。此外,ImF-A导致CD29、CD90和CD105的表达显著降低,而相对端粒长度、成骨、成脂和成软骨能力增强。抗氧化剂处理的ADMSCs与低氧条件下的ADMSCs结果相似。
抗氧化剂处理通过抑制细胞周期蛋白依赖性激酶抑制剂促进ADMSCs进入S期,并导致细胞快速增殖,类似于在低氧条件下观察到的情况。