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

被引:128
|
作者
Kawazoe, Y
Naka, T
Fujimoto, M
Kohzaki, H
Morita, Y
Narazaki, M
Okumura, K
Saitoh, H
Nakagawa, R
Uchiyama, Y
Akira, S
Kishimoto, T
机构
[1] Osaka Univ, Sch Med, Dept Med 3, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Sch Med, Dept Cell Biol & Anat 1, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Dept Host Def, Microbial Dis Res Inst, Suita, Osaka 5650871, Japan
[4] Biomol Engn Res Inst, Suita, Osaka 5650871, Japan
来源
JOURNAL OF EXPERIMENTAL MEDICINE | 2001年 / 193卷 / 02期
关键词
insulin; IRS-1; SSI-1/SOCS1; signaling; janus kinase; diabetes;
D O I
10.1084/jem.193.2.263
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:263 / 269
页数:7
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