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Exp. mol. med ; Exp. mol. med;: 180-189, 2006.
Article in English | WPRIM | ID: wpr-15693

ABSTRACT

In adipocytes, insulin stimulates glucose transport primarily by promoting the translocation of GLUT4 to the plasma membrane. Requirements for Ca2+/ calmodulin during insulin-stimulated GLUT4 translocation have been demonstrated; however, the mechanism of action of Ca2+ in this process is unknown. Recently, myosin II, whose function in non-muscle cells is primarily regulated by phosphorylation of its regulatory light chain by the Ca2+/calmodulin-dependent myosin light chain kinase (MLCK), was implicated in insulin-stimulated GLUT4 translocation. The present studies in 3T3- F442A adipocytes demonstrate the novel finding that insulin significantly increases phosphorylation of the myosin II RLC in a Ca2+-dependent manner. In addition, ML-7, a selective inhibitor of MLCK, as well as inhibitors of myosin II, such as blebbistatin and 2,3-butanedione monoxime, block insulin- stimulated GLUT4 translocation and subsequent glucose transport. Our studies suggest that MLCK may be a regulatory target of Ca2+/calmodulin and may play an important role in insulin-stimulated glucose transport in adipocytes.


Subject(s)
Mice , Animals , Protein Transport/drug effects , Phosphorylation , Naphthalenes/pharmacology , Myosin-Light-Chain Kinase/antagonists & inhibitors , Myosin Type II/metabolism , Insulin/pharmacology , Glucose Transporter Type 4/metabolism , Enzyme Inhibitors/pharmacology , Dose-Response Relationship, Drug , Calmodulin/antagonists & inhibitors , Azepines/pharmacology , Adipocytes/cytology , 3T3 Cells
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