Literature DB >> 8799820

Intracellular targeting of GLUT4 in transfected insulinoma cells: evidence for association with constitutively recycling vesicles distinct from synaptophysin and insulin vesicles.

B Thorens1, J Roth.   

Abstract

In adipocytes and muscle cells, the GLUT4 glucose transporter isoform is present in intracellular vesicles which continuously recycle between an intracytoplasmic location and the plasma membrane. It is not clear whether the GLUT4-vesicles represent a specific kind of vesicle or resemble typical secretory granules or synaptic-like microvesicles. To approach this question, we expressed GLUT4 in the beta cell line RINm5F and determined its intracellular localization by subcellular fractionation and by immunofluorescence and immunoelectron microscopy. GLUT4 was not found in insulin granules but was associated with a subpopulation of smooth-surface vesicles present in the trans-Golgi region and in vesicular structures adjacent to the plasma membrane. In the trans-Golgi region, GLUT4 did not colocalize with synaptophysin or TGN38. Incubation of the cells with horseradish peroxidase (HRP) led to colocalization of HRP and GLUT4 in some endosomal structures adjacent to the plasma membrane and in occasional trans-Golgi region vesicles. When cells were incubated in the presence of Bafilomycin A, analysis by confocal microscopy revealed GLUT4 in numerous large spots present throughout the cytoplasm, many of which costained for TGN38 and synaptophysin. By immunoelectron microscopy, numerous endosomes were observed which stained strongly for GLUT4. Together our data demonstrate that ectopic expression of GLUT4 in insulinoma cells reveals the presence of a subset of vesicular structures distinct from synaptic-like vesicles and insulin secretory granules. Furthermore, they indicate that GLUT4 constitutively recycles between the plasma membrane and its intracellular location by an endocytic route also taken by TGN38 and synaptophysin.

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Year:  1996        PMID: 8799820     DOI: 10.1242/jcs.109.6.1311

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  6 in total

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Authors:  P Arvan; D Castle
Journal:  Biochem J       Date:  1998-06-15       Impact factor: 3.857

2.  Nigericin-induced impairment of autophagic flux in neuronal cells is inhibited by overexpression of Bak.

Authors:  Junghyun Lim; Yunsu Lee; Hyun-Wook Kim; Im Joo Rhyu; Myung Sook Oh; Moussa B H Youdim; Zhenyu Yue; Young J Oh
Journal:  J Biol Chem       Date:  2012-04-05       Impact factor: 5.157

3.  Cerebellar neurons possess a vesicular compartment structurally and functionally similar to Glut4-storage vesicles from peripheral insulin-sensitive tissues.

Authors:  Kyriaki Bakirtzi; Gabriel Belfort; Ignacio Lopez-Coviella; Darshini Kuruppu; Lei Cao; E Dale Abel; Anna-Liisa Brownell; Konstantin V Kandror
Journal:  J Neurosci       Date:  2009-04-22       Impact factor: 6.167

4.  GLUT4 and transferrin receptor are differentially sorted along the endocytic pathway in CHO cells.

Authors:  M L Wei; F Bonzelius; R M Scully; R B Kelly; G A Herman
Journal:  J Cell Biol       Date:  1998-02-09       Impact factor: 10.539

5.  Glucose transporter (GLUT-4) is targeted to secretory granules in rat atrial cardiomyocytes.

Authors:  J W Slot; G Garruti; S Martin; V Oorschot; G Posthuma; E W Kraegen; R Laybutt; G Thibault; D E James
Journal:  J Cell Biol       Date:  1997-06-16       Impact factor: 10.539

6.  Two compartments for insulin-stimulated exocytosis in 3T3-L1 adipocytes defined by endogenous ACRP30 and GLUT4.

Authors:  J S Bogan; H F Lodish
Journal:  J Cell Biol       Date:  1999-08-09       Impact factor: 10.539

  6 in total

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