Department of Physiology, Preclinical School, Xinjiang Medical University, Urumqi, Xinjiang 830011, China.
Evid Based Complement Alternat Med. 2013;2013:287534. doi: 10.1155/2013/287534. Epub 2013 Nov 4.
Ellagic acid (EA) present in many fruits and nuts serves as antiproliferation, anti-inflammatory, and antitumorigenic properties. However, the effect of EA on preadipocytes adipogenesis and its mechanism(s) have not been elucidated. The present study was designed to examine the effect of EA on adipogenesis in 3T3-L1 preadipocytes and underlying mechanism(s) of action involved. Data show that EA administration decreased the accumulation of lipid droplets. The inhibition was diminished when the addition of EA was delayed to days 2-4 of differentiation. Clonal expansion was reduced in the presence of EA. FACS analysis showed that EA blocked the cell cycle at the G1/S transition. EdU incorporation also confirmed that EA refrained cell from entering S phase. Our data also revealed that the differentiation-induced protein expression of Cyclin A and phosphorylation of the retinoblastoma protein (Rb) were impaired by EA. Differentiation-dependent expression and DNA-binding ability of C/EBP α were also inhibited by EA. Alterations in cell cycle-associated proteins may be important with respect to the antiadipogenic action of EA. In conclusion, EA is capable of inhibiting adipogenesis in 3T3-L1 adipocytes possibly through reduction of Cyclin A protein expression and Rb phosphorylation. With the blocking of G1/S phase transition, EA suppresses terminal differentiation and lipid accumulation in 3T3-L1 adipocytes.
鞣花酸(EA)存在于许多水果和坚果中,具有抗增殖、抗炎和抗肿瘤发生的特性。然而,EA 对前体脂肪细胞脂肪生成的影响及其作用机制尚未阐明。本研究旨在研究 EA 对 3T3-L1 前体脂肪细胞脂肪生成的影响及其作用机制。研究数据表明,EA 处理可减少脂滴的积累。当 EA 添加延迟到分化的第 2-4 天,这种抑制作用就会减弱。在 EA 的存在下,克隆扩展减少。FACS 分析显示 EA 在 G1/S 转换时阻止细胞周期。EdU 掺入也证实 EA 阻止细胞进入 S 期。我们的数据还表明,EA 损害了分化诱导的细胞周期蛋白 A 的蛋白表达和视网膜母细胞瘤蛋白(Rb)的磷酸化。EA 还抑制了分化依赖性表达和 C/EBPα的 DNA 结合能力。细胞周期相关蛋白的改变可能与 EA 的抗脂肪生成作用有关。总之,EA 能够抑制 3T3-L1 脂肪细胞的脂肪生成,可能是通过降低细胞周期蛋白 A 的蛋白表达和 Rb 的磷酸化。通过阻止 G1/S 期转换,EA 抑制了 3T3-L1 脂肪细胞的终末分化和脂质积累。