首页> 外文期刊>The Journal of Experomental Medicine >Signal Transducer and Activator of Transcription (Stat)-Induced Stat Inhibitor 1 (Ssi-1)/Suppressor of Cytokine Signaling 1 (Socs1) Inhibits Insulin Signal Transduction Pathway through Modulating Insulin Receptor Substrate 1 (Irs-1) Phosphorylation
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Signal Transducer and Activator of Transcription (Stat)-Induced Stat Inhibitor 1 (Ssi-1)/Suppressor of Cytokine Signaling 1 (Socs1) Inhibits Insulin Signal Transduction Pathway through Modulating Insulin Receptor Substrate 1 (Irs-1) Phosphorylation

机译:信号转导和转录激活(Stat)诱导的Stat抑制剂1(Ssi-1)/细胞因子信号1(Socs1)的抑制剂通过调节胰岛素受体底物1(Irs-1)磷酸化来抑制胰岛素信号转导途径。

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Signal transducer and activator of transcription (STAT)-induced STAT inhibitor 1 (SSI-1) is known to function as a negative feedback regulator of cytokine signaling, but it is unclear whether it is involved in other biological events. Here, we show that SSI-1 participates and plays an important role in the insulin signal transduction pathway. SSI-1–deficient mice showed a significantly low level of blood sugar. While the forced expression of SSI-1 reduced the phosphorylation level of insulin receptor substrate 1 (IRS-1), SSI-1 deficiency resulted in sustained phosphorylation of IRS-1 in response to insulin. Furthermore, SSI-1 achieves this inhibition both by binding directly to IRS-1 and by suppressing Janus kinases. These findings suggest that SSI-1 acts as a negative feedback factor also in the insulin signal transduction pathway through the suppression of IRS-1 phosphorylation.
机译:已知信号转导和转录激活因子(STAT)诱导的STAT抑制剂1(SSI-1)充当细胞因子信号的负反馈调节剂,但尚不清楚它是否参与其他生物学事件。在这里,我们表明SSI-1参与并在胰岛素信号转导途径中起重要作用。缺乏SSI-1的小鼠显示出明显较低的血糖水平。虽然SSI-1的强制表达降低了胰岛素受体底物1(IRS-1)的磷酸化水平,但SSI-1缺乏导致响应胰岛素的IRS-1持续磷酸化。此外,SSI-1通过直接结合IRS-1和抑制Janus激酶来达到这种抑制作用。这些发现表明,通过抑制IRS-1磷酸化,SSI-1在胰岛素信号转导途径中也起着负反馈因子的作用。

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