Abstract
Incubation of isolated GLUT4-containing vesicles with Xenopus oocyte extracts resulted in a guanosine 5′-[γ-thio]triphosphate (GTPγS) and sodium orthovanadate stimulation of actin comet tails. The in vitro actin-based GLUT4 vesicle motility was inhibited by both latrunculin B and a dominant-interfering N-WASP mutant, N-WASP/ΔVCA. Preparations of gently sheared (broken) 3T3L1 adipocytes also displayed GTPγS and sodium orthovanadate stimulation of actin comet tails on GLUT4 intracellular compartments. Furthermore, insulin pretreatment of intact adipocytes prior to gently shearing also resulted in a marked increase in actin polymerization and actin comet tailing on GLUT4 vesicles. In addition, the insulin stimulation of actin comet tails was completely inhibited by Clostridum difficile toxin B, demonstrating a specific role for a Rho family member small GTP-binding protein. Expression of N-WASP/ΔVCA in intact cells had little effect on adipocyte cortical actin but partially inhibited insulin-stimulated GLUT4 translocation. Taken together, these data demonstrate that insulin can induce GLUT4 vesicle actin comet tails that are necessary for the efficient translocation of GLUT4 from intracellular storage sites to the plasma membrane.
Original language | English (US) |
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Pages (from-to) | 49331-49336 |
Number of pages | 6 |
Journal | Journal of Biological Chemistry |
Volume | 276 |
Issue number | 52 |
DOIs | |
State | Published - Dec 28 2001 |
Externally published | Yes |
ASJC Scopus subject areas
- Biochemistry
- Molecular Biology
- Cell Biology