Jeong Jin Young, Park Mi Na, Cho Eun Seok, Jang Hyun-Jun, Park Sungkwon, Lee Hyun-Jeong
Animal Products Utilization Division, National Institute of Animal Science, Rural Development Administration, 1500, Kongjwipatjwi-ro, Iseo-myeon, Wanju-gun, Jeollabuk-do, 565-851, Republic of Korea.
Division of Animal Genomics and Bioinformatics, National Institute of Animal Science, Rural Development Administration, 1500, Kongjwipatjwi-ro, Iseo-myeon, Wanju-gun, Jeollabuk-do, 565-851, Republic of Korea.
Cell Tissue Res. 2015 Oct;362(1):87-96. doi: 10.1007/s00441-015-2191-y. Epub 2015 May 14.
Epigallocatechin-3-gallate (EGCG), a major component of catechin in green tea, has known effects on cancer, diabetes and obesity. We recently reported that the expression levels of various genes and proteins involved in adipogenesis decreases following EGCG treatment. We also assessed apoptosis in EGCG-exposed cells. Here, we explore the variability in free-radical production in bovine bone-marrow mesenchymal stem cells (BMSCs) treated with EGCG. Upon adipogenic differentiation, BMSCs were exposed to various EGCG concentrations (0, 0.1, 1, 5, or 10 μM) for 2, 4, or 6 days. We found that EGCG reduced cell viability and arrested the cell cycle at the gap 2/mitosis phase and that EGCG potentially enhanced the production of free radicals, including reactive oxygen species and reactive nitrogen species, in a concentration- and time-dependent manner. Immunostaining revealed that the expression of genes encoding CCAAT/enhancer-binding protein alpha and stearoyl-CoA desaturase were diminished by EGCG treatment. These findings suggest that EGCG alters free-radical production activity during adipogenic differentiation in BMSCs.
表没食子儿茶素-3-没食子酸酯(EGCG)是绿茶中儿茶素的主要成分,已知其对癌症、糖尿病和肥胖有影响。我们最近报道,EGCG处理后,参与脂肪生成的各种基因和蛋白质的表达水平会降低。我们还评估了EGCG处理的细胞中的细胞凋亡情况。在此,我们探究了用EGCG处理的牛骨髓间充质干细胞(BMSCs)中自由基产生的变异性。在进行脂肪生成分化时,将BMSCs暴露于不同浓度(0、0.1、1、5或10 μM)的EGCG中2、4或6天。我们发现,EGCG降低了细胞活力,并使细胞周期停滞在G2/有丝分裂期,且EGCG可能以浓度和时间依赖性方式增强了包括活性氧和活性氮在内的自由基的产生。免疫染色显示,EGCG处理可降低编码CCAAT/增强子结合蛋白α和硬脂酰辅酶A去饱和酶的基因的表达。这些发现表明,EGCG在BMSCs脂肪生成分化过程中改变了自由基产生活性。