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首页> 外文期刊>Asian-Australasian Journal of Animal Sciences >Conversion of C2C12 myoblast into adipoblast with thiazolidinediones - a possible basis for intramuscular fat generation in meat animals.
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Conversion of C2C12 myoblast into adipoblast with thiazolidinediones - a possible basis for intramuscular fat generation in meat animals.

机译:用噻唑烷二酮将C2C12成肌细胞转化为成脂细胞-肉类动物肌肉内脂肪生成的可能基础。

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Thiazolidinediones (TZDs) act as potent activators of the adipose differentiation program in established preadipose cell lines. TZD's have also been investigated in diabetic patients and reported to act as PPAR- gamma ligands. In this report, the effects of TZDs on the differentiation pathway of myoblasts have been investigated. C2C12 mouse myoblasts were grown in Dulbecco's Modified Eagles medium for 4-5 days until they reached almost 100% confluency. Post-confluent cells (day 0) were further exposed to adipogenic induction medium along with TZDs for 48 hours. Thereafter, cells were exposed only to TZDs every 48 h until day 10. The control was provided with differentiation medium without any treatment. Alterations in the cells during the differentiation programme were analysed on the basis of fusion index, oil-red-o staining, adipocyte index, adipocyte stain uptake measurement, immuno-histochemistry and western blotting. Exposure of C2C12 mouse myoblasts to TZDs prevented the expression of myosin heavy chain with parallel increase in the expression of C/EBP- alpha and PPAR- gamma and acquisition of adipocyte morphology, thus abolishing the formation of multinucleated myotubes. TZDs exert their adipogenic effects only in non-terminally differentiated myoblasts; myotubes were insensitive to the compound. Continuous exposure (at least 4-5 doses) to inducers after the growth arrest was essential to provide a sustained environment to the cells converting to fully matured adipocytes. The results indicate that TZDs specifically converted the differentiation pathway of myoblasts into that of adipoblasts..
机译:噻唑烷二酮(TZD)在已建立的脂肪细胞系中作为脂肪分化程序的有效激活剂。 TZD也已在糖尿病患者中进行了研究,并据报道可作为PPAR-γ配体。在本报告中,已经研究了TZDs对成肌细胞分化途径的影响。 C2C12小鼠成肌细胞在Dulbecco的改良Eagles培养基中生长4-5天,直到它们达到几乎100%融合为止。汇合后的细胞(第0天)进一步与TZD一起暴露于成脂诱导培养基中48小时。之后,每48小时仅将细胞暴露于TZD,直到第10天。为对照提供分化培养基,无需任何处理。根据融合指数,油红-o染色,脂肪细胞指数,脂肪细胞染色摄取测量,免疫组织化学和蛋白质印迹分析了分化程序中细胞的变化。将C2C12小鼠成肌细胞暴露于TZD会阻止肌球蛋白重链的表达,同时增加C /EBP-α和PPAR-γ的表达并获得脂肪细胞形态,从而消除了多核肌管的形成。 TZD仅在非终末分化的成肌细胞中发挥其成脂作用。肌管对该化合物不敏感。生长停滞后连续暴露于诱导剂(至少4-5剂)对于为转化为完全成熟的脂肪细胞的细胞提供持续的环境至关重要。结果表明,TZDs特异地将成肌细胞的分化途径转化为成脂细胞的分化途径。

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