方心灵, 王海峰, 束 刚, 王松波, 朱晓彤, 王丽娜, 高 萍, 江青艳. 山梨酸对C2C12细胞增殖、IGF-1分泌和相关基因表达的影响[J]. 华南农业大学学报, 2012, 33(4): 529-534. DOI: 10.7671/j.issn.1001-411X.2012.04.020
    引用本文: 方心灵, 王海峰, 束 刚, 王松波, 朱晓彤, 王丽娜, 高 萍, 江青艳. 山梨酸对C2C12细胞增殖、IGF-1分泌和相关基因表达的影响[J]. 华南农业大学学报, 2012, 33(4): 529-534. DOI: 10.7671/j.issn.1001-411X.2012.04.020
    FANG Xin-ling, WANG Hai-feng, SHU Gang, WANG Song-bo, ZHU Xiao-tong, WANG Li-na, GAO Ping, JIANG Qing-yan. Effects of Sorbic Acid on Proliferation, IGF-1 Secretion and Related Gene mRNA Expression in C2C12 Cell[J]. Journal of South China Agricultural University, 2012, 33(4): 529-534. DOI: 10.7671/j.issn.1001-411X.2012.04.020
    Citation: FANG Xin-ling, WANG Hai-feng, SHU Gang, WANG Song-bo, ZHU Xiao-tong, WANG Li-na, GAO Ping, JIANG Qing-yan. Effects of Sorbic Acid on Proliferation, IGF-1 Secretion and Related Gene mRNA Expression in C2C12 Cell[J]. Journal of South China Agricultural University, 2012, 33(4): 529-534. DOI: 10.7671/j.issn.1001-411X.2012.04.020

    山梨酸对C2C12细胞增殖、IGF-1分泌和相关基因表达的影响

    Effects of Sorbic Acid on Proliferation, IGF-1 Secretion and Related Gene mRNA Expression in C2C12 Cell

    • 摘要: 为研究山梨酸对小鼠骨骼肌成肌细胞(C2C12)增殖、IGF-1分泌、GH/IGF系统和糖脂代谢相关基因表达的影响,试验通过培养基中添加不同浓度的山梨酸(0、0.1、1.0、10.0和100.0 μmol/L)处理C2C12细胞,采用MTT法检测细胞增殖,RIA法检测细胞IGF-1分泌量,qPCR法检测相关基因mRNA的表达水平.结果表明:1)10.0 μmol/L山梨酸显著促进体积分数为10%胎牛血清(1和2 d)和无血清(4和5 d)培养的C2C12细胞增殖(P<0.05); 2)0.1、1.0和100.0 μmol/L山梨酸均显著抑制无血清培养的C2C12细胞IGF-1的分泌(P <0.05); 3)1.0 μmol/L山梨酸显著上调无血清培养的C2C12细胞IGF-1R、GHR和CPT1b的mRNA表达(P<0.05),对IGFBP3(P=0.09)、PDK4(P=0.10)和PGC1α(P=0.10)的mRNA表达量也有提高趋势.提示山梨酸可促进C2C12细胞的增殖和GH/IGF系统及糖脂代谢相关基因mRNA表达,但对IGF-1的分泌具有抑制作用.

       

      Abstract: The purpose of this experiment was to explore the effects of sorbic acid(SA) on proliferation, IGF-1 secretion, GH/IGF system and glucose and lipid metabolism-related genes mRNA expression in C2C12 cells. C2C12 cells were exposed to different doses of SA(0, 0.1, 1.0, 10.0 and 100.0 μmol/L)to measure cell proliferation by MTT assay, IGF-1 secretion by RIA assay and transcript levels by qPCR assay. Results indicated that: 1) SA(10.0 μmol/L) significantly promoted(P<0.05) proliferation of cell cultured with 10% fetal bovine serum(1 and 2 d) or without serum(4 and 5 d). 2) IGF-1 secretion was significantly suppressed(P<0.05) by 0.1, 1.0 or 100.0 μmol/L SA in serum-free cultured C2C12 cells. 3) Expressions of IGF-1R, GHR and CPT1b mRNA were significantly up-regulated in serum-free cultured C2C12 cells treated with 1.0 μmol/L SA. The increasing trend of IGFBP3 (P=0.09), PDK4 (P=0.10) and PGC1 α(P=0.10) transcript levels were also observed in serum-free cultured C2C12 cells by 1.0 μmol/L SA treatment. This suggested that SA could increase proliferation and GH/IGF system and glucose and lipid metabolism-related genes mRNA expression but depress IGF-1 secretion in C2C12 cells.

       

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