| Literature DB >> 27929607 |
Zhou Zhou1,2, Franziska Menzel3, Tim Benninghoff1,2, Alexandra Chadt1,2, Chen Du1, Geoffrey D Holman4, Hadi Al-Hasani1,2.
Abstract
The Rab-GTPase-activating proteins (GAPs) TBC1D1 and TBC1D4 play important roles in the insulin-stimulated translocation of the glucose transporter GLUT4 from intracellular vesicles to the plasma membrane in muscle cells and adipocytes. We identified Rab28 as a substrate for the GAP domains of both TBC1D1 and TBC1D4 in vitro. Rab28 is expressed in adipose cells and skeletal muscle, and its GTP-binding state is acutely regulated by insulin. We found that in intact isolated mouse skeletal muscle, siRNA-mediated knockdown of Rab28 decreases basal glucose uptake. Conversely, in primary rat adipose cells, overexpression of Rab28-Q72L, a constitutively active mutant, increases basal cell surface levels of an epitope-tagged HA-GLUT4. Our results indicate that Rab28 is a novel GTPase involved in the intracellular retention of GLUT4 in insulin target cells.Entities:
Keywords: GLUT4; GTPase; adipose tissue; insulin signaling; skeletal muscle
Mesh:
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Year: 2016 PMID: 27929607 DOI: 10.1002/1873-3468.12509
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124