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Insulin signaling in adipocytes differentiated from mouse stromal MC3T3-G2/PA6 cells

机译:与小鼠基质MC3T3-G2 / PA6细胞分化的脂肪细胞中的胰岛素信号传导

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The stromal MC3T3-G2/PA6 (PA6) cells from mouse clavaria did not require insulin for differentiation into mature adipose cells, although insulin is well known to play a key role in adipocyte differentiation. Large lipid droplets were observed in the cytoplasm of PA6 cells, and mRNA expression of the adipose specific proteins (aP2, PPAR gamma, C/EBP alpha, FAS, GLUT4, leptin, and adiponectin) as differentiation markers appeared or increased clearly in the cells at 8 d after stimulation without insulin. In addition, the glycerol released from the cells (lipolysis) was increased in a concentration-dependent manner by isoproterenol. However, the isoproterenol-induced lipolysis in the cells was not influenced by treatment with insulin, although that was observed in extramedullary adipocytes, 3T3-L1 cells. On the other hand, the 2-deoxy-D-[1-H-3]glucose uptake in differentiated PA6 cells also increased by insulin, as shown in other adipose cells. In the cells, insulin induced the phosphorylation of extracellular signal-regulated kinases (Erks), Akt at Ser 473 and ribosomal p70 S6 protein kinase (p70 S6K) at Thr 389, and the insulin-induced 2-deoxy-D-[1-H-3]glucose uptake was inhibited by pre-treatment with wortmannin, an inhibitor of phosphatidylinositol 3-kinase (PI3K), or NIL-9, an Akt inhibitor. These results suggest that the insulin signal for adipogenesis (lipogenesis) and lipolysis in bone marrow stroma PA6 cells differs from extramedullary adipocytes, such as 3T3-L1 cells.
机译:尽管众所周知胰岛素在脂肪细胞分化中起关键作用,但来自小鼠小肠的基质MC3T3-G2 / PA6(PA6)细胞不需要胰岛素即可分化为成熟的脂肪细胞。在PA6细胞的细胞质中观察到大的脂滴,并且脂肪特异性蛋白质(aP2,PPARγ,C / EBPα,FAS,GLUT4,瘦素和脂联素)的mRNA表达在细胞中出现或明显增加在无胰岛素刺激后第8天。另外,异丙肾上腺素以浓度依赖的方式增加从细胞释放的甘油(脂解)。然而,尽管在髓外脂肪细胞,3T3-L1细胞中观察到了胰岛素的作用,但异丙肾上腺素诱导的细胞中的脂解作用并未受到胰岛素治疗的影响。另一方面,如在其他脂肪细胞中所示,分化的PA6细胞中的2-脱氧-D- [1-H-3]葡萄糖摄取也被胰岛素增加。在细胞中,胰岛素诱导细胞外信号调节激酶(Erks),Ser 473的Akt和Thr 389的核糖体p70 S6蛋白激酶(p70 S6K)的磷酸化,以及胰岛素诱导的2-deoxy-D- [1- H-3]葡萄糖的摄取受到渥曼青霉素(磷脂酰肌醇3-激酶(PI3K)的抑制剂)或NIL-9(Akt抑制剂)的预处理的抑制。这些结果表明,骨髓基质PA6细胞中用于脂肪形成(脂肪生成)和脂解的胰岛素信号不同于髓外脂肪细胞,例如3T3-L1细胞。

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