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胰岛素和 IGF-1 对 3T3-F442A 脂肪细胞中生长激素诱导的 STAT5 激活的影响。

Effects of insulin and IGF-I on growth hormone- induced STAT5 activation in 3T3-F442A adipocytes.

机构信息

The Institute of Cell Biology, Shandong University School of Medicine, Jinan 250012, China.

出版信息

Lipids Health Dis. 2013 Apr 30;12:56. doi: 10.1186/1476-511X-12-56.

Abstract

BACKGROUND

Growth hormone (GH) and insulin signaling pathways are known important regulators of adipose homeostasis. The cross-talk between GH and insulin signaling pathways in mature adipocytes is poorly understood.

METHODS

In the present study, the impact of insulin on GH-mediated signaling in differentiated 3T3-F442A adipocytes and primary mice adipocytes was examined.

RESULTS

Insulin alone did not induce STAT5 tyrosine phosphorylation, but enhanced GH-induced STAT5 activation. This effect was more pronounced when insulin was added 20 min prior to GH treatment. The above results were further confirmed by in vivo study, showing that insulin pretreatment potentiated GH- induced STAT5 tyrosine phosphorylation in visceral adipose tissues of C57/BL6 mice. In addition, our in vitro results showed that IGF-I had similar potentiating effect as insulin on GH-induced STAT5 activation. In vitro, insulin and IGF-I had an additive effect on GH- induced MAPK activation.

CONCLUSION

These results indicate that both insulin and IGF-I specifically potentiated GH mediated STAT5 activation in mature adipose cells. These findings suggest that insulin and GH, usually with antagonistic functions, might act synergistically to regulate some specific functions in mature adipocytes.

摘要

背景

生长激素(GH)和胰岛素信号通路是已知的脂肪稳态的重要调节因子。成熟脂肪细胞中 GH 和胰岛素信号通路之间的串扰知之甚少。

方法

本研究探讨了胰岛素对分化的 3T3-F442A 脂肪细胞和原代小鼠脂肪细胞中 GH 介导的信号转导的影响。

结果

胰岛素本身不会诱导 STAT5 酪氨酸磷酸化,但增强了 GH 诱导的 STAT5 激活。当胰岛素在 GH 处理前 20 分钟添加时,这种作用更为明显。体内研究进一步证实了上述结果,表明胰岛素预处理增强了 C57/BL6 小鼠内脏脂肪组织中 GH 诱导的 STAT5 酪氨酸磷酸化。此外,我们的体外结果表明,IGF-I 对 GH 诱导的 STAT5 激活具有与胰岛素相似的增强作用。在体外,胰岛素和 IGF-I 对 GH 诱导的 MAPK 激活具有相加作用。

结论

这些结果表明,胰岛素和 IGF-I 均可特异性增强成熟脂肪细胞中 GH 介导的 STAT5 激活。这些发现表明,胰岛素和 GH 通常具有拮抗作用,可能在调节成熟脂肪细胞中的某些特定功能方面发挥协同作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52b2/3653719/058fe4de001a/1476-511X-12-56-1.jpg

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