Mau Marcus, Kalbe Claudia, Wollenhaupt Karin, Nürnberg Gerd, Rehfeldt Charlotte
Research Unit Muscle Biology and Growth, Research Institute for the Biology of Farm Animals, Wilhelm-Stahl-Allee 2, 18196 Dummerstorf, Germany.
Domest Anim Endocrinol. 2008 Oct;35(3):281-9. doi: 10.1016/j.domaniend.2008.06.004. Epub 2008 Jul 11.
Soy-derived isoflavones have been reported to be specific inhibitors of protein tyrosine kinases like the type 1 insulin-like growth factor receptor (IGF-1R) and the epidermal growth factor receptor (EGFR). This study was conducted to investigate, whether IGF-I and EGF stimulate porcine myoblast growth and whether the responses are influenced by isoflavones. Satellite cell-born myoblasts derived from the semimembranosus muscle of newborn piglets were treated for 26 h with IGF-I or EGF alone and in combination with genistein or daidzein. The DNA amount was measured and DNA synthesis was recorded as 6 h-[(3)H]thymidine incorporation during exponential growth in serum-free basal medium. IGF-I and EGF synergistically stimulated DNA synthesis of porcine myoblast with EGF causing a greater response. Genistein (100 micromol/l) effectively reduced the growth factor-mediated DNA synthesis, which was associated with an inhibition of growth factor receptor protein expression. In response to daidzein no reduction in growth factor-mediated DNA synthesis was found. Daidzein (1; 10 micromol/l) combined with IGF-I caused even a slight increase in DNA amount compared with the untreated control. The expression of the IGF-1R precursor protein was reduced with 10 and 100 micromol/l daidzein, whereas the EGFR expression remained unchanged with daidzein. The results suggest that dietary isoflavones may interact with growth factor-induced stimulation of pig skeletal muscle growth.
据报道,大豆来源的异黄酮是蛋白酪氨酸激酶的特异性抑制剂,如1型胰岛素样生长因子受体(IGF-1R)和表皮生长因子受体(EGFR)。本研究旨在调查IGF-I和EGF是否刺激猪成肌细胞生长,以及这些反应是否受异黄酮影响。将新生仔猪半膜肌来源的卫星细胞衍生的成肌细胞单独用IGF-I或EGF处理26小时,并与染料木黄酮或大豆苷元联合处理。在无血清基础培养基中指数生长期间,测量DNA含量并将DNA合成记录为6小时-[(3)H]胸腺嘧啶核苷掺入量。IGF-I和EGF协同刺激猪成肌细胞的DNA合成,其中EGF引起更大的反应。染料木黄酮(100微摩尔/升)有效降低生长因子介导的DNA合成,这与生长因子受体蛋白表达的抑制有关。对于大豆苷元,未发现生长因子介导的DNA合成减少。与未处理的对照相比,大豆苷元(1;10微摩尔/升)与IGF-I联合使用甚至使DNA量略有增加。10和100微摩尔/升大豆苷元可降低IGF-1R前体蛋白的表达,而大豆苷元处理后EGFR表达保持不变。结果表明,膳食异黄酮可能与生长因子诱导的猪骨骼肌生长刺激相互作用。