» Articles » PMID: 19076072

The C-terminus of GLUT4 Targets the Transporter to the Perinuclear Compartment but Not to the Insulin-responsive Vesicles

Overview
Journal Biochem J
Specialty Biochemistry
Date 2008 Dec 17
PMID 19076072
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Postprandial blood glucose clearance is mediated by GLUT4 (glucose transporter 4) which is translocated from an intracellular storage pool to the plasma membrane in response to insulin. The nature of the intracellular storage pool of GLUT4 is not well understood. Immunofluorescence staining shows that, under basal conditions, the major population of GLUT4 resides in the perinuclear compartment. At the same time, biochemical fractionation reveals that GLUT4 is localized in IRVs (insulin-responsive vesicles). The relationship between the perinuclear GLUT4 compartment and the IRVs is not known. In the present study, we have exchanged the C-termini of GLUT4 and cellugyrin, another vesicular protein that is not localized in the IRVs and has no insulin response. We have found that GLUT4 with the cellugyrin C-terminus loses its specific perinuclear localization, whereas cellugyrin with the GLUT4 C-terminus acquires perinuclear localization and becomes co-localized with GLUT4. This, however, is not sufficient for the effective entry of the latter chimaera into the IRVs as only a small fraction of cellugyrin with the GLUT4 C-terminus is targeted to the IRVs and is translocated to the plasma membrane in response to insulin stimulation. We suggest that the perinuclear GLUT4 storage compartment comprises the IRVs and the donor membranes from which the IRVs originate. The C-terminus of GLUT4 is required for protein targeting to the perinuclear donor membranes, but not to the IRVs.

Citing Articles

Insulin-promoted mobilization of GLUT4 from a perinuclear storage site requires RAB10.

Brumfield A, Chaudhary N, Molle D, Wen J, Graumann J, McGraw T Mol Biol Cell. 2020; 32(1):57-73.

PMID: 33175605 PMC: 8098823. DOI: 10.1091/mbc.E20-06-0356.


BAG6 contributes to glucose uptake by supporting the cell surface translocation of the glucose transporter GLUT4.

Minami S, Yokota N, Kawahara H Biol Open. 2020; 9(1).

PMID: 31911483 PMC: 6994957. DOI: 10.1242/bio.047324.


Mitochondrial Ultrastructure and Glucose Signaling Pathways Attributed to the Kv1.3 Ion Channel.

Kovach C, Al Koborssy D, Huang Z, Chelette B, Fadool J, Fadool D Front Physiol. 2016; 7:178.

PMID: 27242550 PMC: 4871887. DOI: 10.3389/fphys.2016.00178.


Alternative routes to the cell surface underpin insulin-regulated membrane trafficking of GLUT4.

Kioumourtzoglou D, Pryor P, Gould G, Bryant N J Cell Sci. 2015; 128(14):2423-9.

PMID: 26071524 PMC: 4510850. DOI: 10.1242/jcs.166561.


Dynamic GLUT4 sorting through a syntaxin-6 compartment in muscle cells is derailed by insulin resistance-causing ceramide.

Foley K, Klip A Biol Open. 2014; 3(5):314-25.

PMID: 24705014 PMC: 4021353. DOI: 10.1242/bio.20147898.


References
1.
Perera H, Clarke M, Morris N, Hong W, Chamberlain L, Gould G . Syntaxin 6 regulates Glut4 trafficking in 3T3-L1 adipocytes. Mol Biol Cell. 2003; 14(7):2946-58. PMC: 165689. DOI: 10.1091/mbc.e02-11-0722. View

2.
Corvera S, Chawla A, Chakrabarti R, Joly M, Buxton J, Czech M . A double leucine within the GLUT4 glucose transporter COOH-terminal domain functions as an endocytosis signal. J Cell Biol. 1994; 126(4):979-89. PMC: 2120130. DOI: 10.1083/jcb.126.4.979. View

3.
Laemmli U . Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970; 227(5259):680-5. DOI: 10.1038/227680a0. View

4.
Asano T, Takata K, Katagiri H, Tsukuda K, Lin J, Ishihara H . Domains responsible for the differential targeting of glucose transporter isoforms. J Biol Chem. 1992; 267(27):19636-41. View

5.
Blot V, McGraw T . GLUT4 is internalized by a cholesterol-dependent nystatin-sensitive mechanism inhibited by insulin. EMBO J. 2006; 25(24):5648-58. PMC: 1698906. DOI: 10.1038/sj.emboj.7601462. View