华南预防医学 ›› 2013, Vol. 39 ›› Issue (5): 1-5.

• 论著 •    下一篇

白藜芦醇对小鼠前脂肪细胞凋亡及细胞周期的影响

黎文明,张翔,谭炳炎,于志文,郑琳,高渊,杨芳,冯翔   

  1. 中山大学公共卫生学院,广东广州510080
  • 出版日期:2013-10-20 发布日期:2014-03-24
  • 作者简介:黎文明(1987-),男,硕士,主要研究方向:营养与健康
  • 基金资助:
    广东省建设中医药强省课题(No.20111157)

Effect of resveratrol on cell cycle and apoptosis in 3T3-L1 preadipocytes

LI Wen-ming, ZHANG Xiang, TAN Bing-yan, YU Zhi-wen, ZHENG Lin, GAO Yuan, YANG Fang, FENG Xiang.   

  1. School of Public Health,SunYat-sen University,Guangzhou 510080,China
  • Online:2013-10-20 Published:2014-03-24
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摘要: 目的 研究白藜芦醇(Res)对小鼠前脂肪细胞凋亡及细胞周期的影响及其机制?方法 分别用25?50?75?100μmol/L的Res干预小鼠前脂肪细胞24?48?72h,并设0μmol/L Res为阴性对照组(每组设3个复孔,重复3次)?全自动倒置荧光显微镜观察细胞的形态学变化?细胞增殖-毒性检测试剂盒检测细胞增殖活性?流式细胞仪检测细胞凋亡与细胞周期?结果 形态学上,经50μmol/L Res干预48h后的小鼠前脂肪细胞具有典型凋亡形态学改变?细胞增殖-毒性检测发现,0?25?50?75?100μmol/L Res干预24h细胞增殖率分别为100%?(97.00±1.00)%?(91.00±2.65)%?(90.67±2.52)%和(86.00±3.61)%;干预48h细胞增殖率分别是100%?(86.67±2.52)%?(76.00±2.00)%?(34.33±2.08)%和(30.33±2.52)%;干预72h,细胞增殖率分别是100%?(82.00±2.65)%?(65.67±3.06)%?(21.00±3.61)%和(16.33±3.21)%?偏相关分析结果显示细胞增殖率与干预时间?Res浓度均呈负相关关系(r=-0.72?-0.83,均P<0.01)?0?25?50?75?100μmol/L Res干预24h,G0/G1期的细胞比例分别为(27.23±2.63)%?(39.03±2.74)%?(80.20±5.15)%?(87.97±3.12)%和(90.80±2.08)%;S期的细胞比例分别为(72.43±2.99)%?(63.93±6.90)%?(19.80±5.15)%?(12.20±2.86)%和(9.20±2.08)%,2个细胞周期的50?75?100μmol/L Res干预组与阴性对照组之间的细胞比例差异均有统计学意义(P<0.05或P<0.01)?0?25?50?75?100μmol/L Res干预48h,细胞凋亡率分别为(2.90±0.10)%?(5.40±3.81)%?(8.23±4.24)%?(29.77±6.18)% 和(27.23±3.17)%;细胞坏死率分别为(7.50±0.87)%?(12.00±4.89)%?(12.27±3.81)%?(12.67±6.13)%和(20.73±2.64)%,100μmol/L的干预组的细胞调亡率?坏死率与阴性对照组的差异均具有统计学意义(P<0.05或P<0.01),其他各组与阴性对照组的差异均无统计学意义(P>0.05)?结论 在一定的剂量范围内(0~100μmol/L),Res 可能抑制小鼠前脂肪细胞生命周期并促进其凋亡?

Abstract: Objective To study the effects and mechanism of resveratrol(Res) on apoptosis and cell cycle in 3T3-L1 preadipocytes. Methods 3T3-L1 preadipocytes were treated with different doses of Restreatment (0,25,50,75,and 100μmol/L, 0μmol/Las the negative control) for 24, 48 or 72h. The Fluorescence microscope, MTT assay,and flow-cytometry were used for measuring cell morphology, cell proliferation, cell cycle, and apoptosis. Results After treated with 50μmol/L of Res for 48h, 3T3-L1 preadipocytes exhibited typical apoptosis features when observed under fluorescence microscope. MTT assay showed that, after different doses of Res treatment (0, 25, 50, 75, and 100μmol/L) for 24h, cell proliferation rate was 100%, (97.00 ±1.00)%, (91.00 ±2.65)%, (90.67 ±2.52)%, and (86.00±3.61)%, respectively; after the similar Res treatment for 48h, cell proliferation rate was 100%, (86.67±2.52)%, (76.00±2.00)%, (34.33±2.08)%, and(30.33±2.52)%, respectively; also, after the similar Res treatment for 72 h, cell proliferation rate was 100%, (82.00±2.65)%, (65.67±3.06)%, (21.00±3.61)%, and (16.33±3.21)%, respectively. Partial correlation analysis showed a negative correlation between cell proliferation rate and intervention time, concentration of Res (r=-0.72?-0.83, all P<0.01). After different doses of Res treatment (0, 25, 50, 75, and 100μmol/L) for 24h, the portion of cells in G0/G1 phase was (27.23±2.63)%, (39.03±2.74)%, (80.20±5.15)%, (87.97±3.12)%, (90.80±2.08)%, respectively; as the same, the portion of cells In S phase was (72.43±2.99)%, (63.93±6.90)%, (19.80±5.15)%, (12.20±2.86)%, (9.20±2.08)%, respectively. From the results of the cell cycle examination, the portion of cells in G0/G1 phase decreased (P<0.05orP <0.01) and increased evidently in S phase (P<0.05 or P < 0.01) in a dose dependent manner. After different doses of Res treatment (0, 25, 50, 75, 100μmol/L) for 48h, apoptosis rate was (2.90±0.10)%, (5.40±3.81)%, (8.23±4.24)%, (29.77±6.18)%, (27.23±3.17)%, respectively; as the same, necrosis rate was (7.50±0.87)%, (12.00±4.89)%, (12.27±3.81)%, (12.67±6.13)%, (20.73±2.64)%, respectively. The apoptosis and necrosis of 3T3-L1 preadipocytes were statistically significant different between 100μmol/L Res group and negative control group (P<0.05 or P<0.01). Conclusion At a certain dose range (0-100μmol/L), Res may inhibit the life cycle and promote apoptosis of 3T3-L1 preadipocytes.

中图分类号: 

  • R589.2