Literature DB >> 18171432

The mass action hypothesis: formation of Glut4 storage vesicles, a tissue-specific, regulated exocytic compartment.

P F Pilch1.   

Abstract

Insulin stimulates glucose uptake into the target tissues of fat and muscle by recruiting or translocating Glut4 glucose transport proteins to their functional location at the cell surface. In the basal state, Glut4 is sequestered intracellularly in several vesicular compartments, one of which has come to be known as Glut4 storage vesicles (GSVs). The GSVs represent a tissue-specific compartment that is an ultimate target of the insulin signalling cascade. Glut4 translocation has been extensively studied because of its intrinsic scientific importance to cell biology as well as its relevance to the pathology of type 2 diabetes mellitus. I review herein the ontogeny of GSVs and their composition as it relates to a tissue-specific, hormone-sensitive exocytic compartment and propose a mechanism for their formation.

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Year:  2008        PMID: 18171432     DOI: 10.1111/j.1748-1716.2007.01788.x

Source DB:  PubMed          Journal:  Acta Physiol (Oxf)        ISSN: 1748-1708            Impact factor:   6.311


  15 in total

1.  Single nucleotide polymorphisms within functional regions of genes implicated in insulin action and association with the insulin resistant phenotype.

Authors:  Malgorzata Malodobra; Agnieszka Pilecka; Bohdan Gworys; Rajmund Adamiec
Journal:  Mol Cell Biochem       Date:  2010-11-27       Impact factor: 3.396

Review 2.  A proteolytic pathway that controls glucose uptake in fat and muscle.

Authors:  Jonathan P Belman; Estifanos N Habtemichael; Jonathan S Bogan
Journal:  Rev Endocr Metab Disord       Date:  2014-03       Impact factor: 6.514

3.  Coordinated Regulation of Vasopressin Inactivation and Glucose Uptake by Action of TUG Protein in Muscle.

Authors:  Estifanos N Habtemichael; Abel Alcázar-Román; Bradley R Rubin; Laura R Grossi; Jonathan P Belman; Omar Julca; Michael G Löffler; Hongjie Li; Nai-Wen Chi; Varman T Samuel; Jonathan S Bogan
Journal:  J Biol Chem       Date:  2015-05-05       Impact factor: 5.157

4.  Caveolins/caveolae protect adipocytes from fatty acid-mediated lipotoxicity.

Authors:  Tova Meshulam; Michael R Breen; Libin Liu; Robert G Parton; Paul F Pilch
Journal:  J Lipid Res       Date:  2011-06-07       Impact factor: 5.922

5.  Sortilin 1 knockout alters basal adipose glucose metabolism but not diet-induced obesity in mice.

Authors:  Jibiao Li; David J Matye; Yifeng Wang; Tiangang Li
Journal:  FEBS Lett       Date:  2017-03-16       Impact factor: 4.124

6.  Sac3 is an insulin-regulated phosphatidylinositol 3,5-bisphosphate phosphatase: gain in insulin responsiveness through Sac3 down-regulation in adipocytes.

Authors:  Ognian C Ikonomov; Diego Sbrissa; Takeshi Ijuin; Tadaomi Takenawa; Assia Shisheva
Journal:  J Biol Chem       Date:  2009-07-03       Impact factor: 5.157

7.  Proteomic analysis of GLUT4 storage vesicles reveals LRP1 to be an important vesicle component and target of insulin signaling.

Authors:  Mark P Jedrychowski; Carlos A Gartner; Steven P Gygi; Li Zhou; Joachim Herz; Konstantin V Kandror; Paul F Pilch
Journal:  J Biol Chem       Date:  2009-10-28       Impact factor: 5.157

Review 8.  Phosphoinositides in insulin action on GLUT4 dynamics: not just PtdIns(3,4,5)P3.

Authors:  Assia Shisheva
Journal:  Am J Physiol Endocrinol Metab       Date:  2008-05-20       Impact factor: 4.310

9.  Deletion of Cavin/PTRF causes global loss of caveolae, dyslipidemia, and glucose intolerance.

Authors:  Libin Liu; Dennis Brown; Mary McKee; Nathan K Lebrasseur; Dan Yang; Kenneth H Albrecht; Katya Ravid; Paul F Pilch
Journal:  Cell Metab       Date:  2008-10       Impact factor: 27.287

Review 10.  Clathrin-independent endocytosis: a unique platform for cell signaling and PM remodeling.

Authors:  Julie G Donaldson; Natalie Porat-Shliom; Lee Ann Cohen
Journal:  Cell Signal       Date:  2008-07-03       Impact factor: 4.315

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