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Tiam-1, a GEF for Rac1, plays a critical role in metformin-mediated glucose uptake in C2C12 cells
- Source :
- Cellular Signalling. 25:2558-2565
- Publication Year :
- 2013
- Publisher :
- Elsevier BV, 2013.
-
Abstract
- 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.
- Subjects :
- rac1 GTP-Binding Protein
endocrine system diseases
Glucose uptake
RAC1
AMP-Activated Protein Kinases
Cell Line
Mice
PAK1
AMP-activated protein kinase
medicine
Animals
Guanine Nucleotide Exchange Factors
Hypoglycemic Agents
T-Lymphoma Invasion and Metastasis-inducing Protein 1
RNA, Messenger
Phosphorylation
Muscle, Skeletal
biology
Kinase
Chemistry
nutritional and metabolic diseases
AMPK
Cell Biology
Ribonucleotides
Aminoimidazole Carboxamide
Metformin
Up-Regulation
Cell biology
Glucose
p21-Activated Kinases
biology.protein
medicine.drug
Subjects
Details
- ISSN :
- 08986568
- Volume :
- 25
- Database :
- OpenAIRE
- Journal :
- Cellular Signalling
- Accession number :
- edsair.doi.dedup.....70800f1f9c9bf774e90d5f2c77b440dc
- Full Text :
- https://doi.org/10.1016/j.cellsig.2013.08.018