You Ga Young, Lee Jung Ok, Kim Ji Hae, Kim Nami, Lee Soo Kyung, Moon Ji Wook, Jie Sha, Lee Hye Jeong, Kim Su Jin, Park Sun Hwa, Kim Hyeon Soo
Department of Anatomy, Korea University College of Medicine, Seoul, Republic of Korea.
Cell Signal. 2013 Dec;25(12):2558-65. doi: 10.1016/j.cellsig.2013.08.018. Epub 2013 Aug 29.
Metformin is known to stimulate glucose uptake, but the mechanism for this action is not fully understood. In this study, AMPK activators (AICAR and metformin) increased the expression of T-lymphoma invasion and metastasis-inducing protein-1 (Tiam-1), a Rac1 specific guanine nucleotide exchange factor (GEF), mRNA and protein in skeletal muscle C2C12 cells. Metformin increases the serine-phosphorylation of Tiam-1 by AMPK and induces interaction between Tiam-1 and 14-3-3. Pharmacologic inhibition of AMPK blocks this interaction, indicating that 14-3-3 may be required for induction of Tiam-1 by AMPK. Metformin also increases the phosphorylation of p21-activated kinase 1 (PAK1), a direct downstream target of Rac1, dependent on AMPK. Tiam-1 is down-regulated at high glucose concentrations in cultured cells and in the db/db mouse model of hyperglycemia. Furthermore, Tiam-1 knock-down blocked metformin-induced increase in glucose uptake. These findings suggest that metformin promotes cellular glucose uptake in part through Tiam-1 induction.
已知二甲双胍可刺激葡萄糖摄取,但其作用机制尚未完全明确。在本研究中,AMPK激活剂(AICAR和二甲双胍)可增加骨骼肌C2C12细胞中T淋巴瘤侵袭与转移诱导蛋白-1(Tiam-1,一种Rac1特异性鸟嘌呤核苷酸交换因子(GEF))的mRNA和蛋白表达。二甲双胍通过AMPK增加Tiam-1的丝氨酸磷酸化,并诱导Tiam-1与14-3-3之间的相互作用。对AMPK的药理抑制可阻断这种相互作用,表明14-3-3可能是AMPK诱导Tiam-1所必需的。二甲双胍还可增加p21激活激酶1(PAK1,Rac1的直接下游靶点)的磷酸化,且该作用依赖于AMPK。在培养细胞和糖尿病(db/db)高血糖小鼠模型中,高葡萄糖浓度会使Tiam-1表达下调。此外,敲低Tiam-1可阻断二甲双胍诱导的葡萄糖摄取增加。这些发现提示,二甲双胍部分通过诱导Tiam-1来促进细胞葡萄糖摄取。