Literature DB >> 12479577

Giant membrane vesicles as a model to study cellular substrate uptake dissected from metabolism.

D P Y Koonen1, W A Coumans, Y Arumugam, A Bonen, J F C Glatz, J J F P Luiken.   

Abstract

In order to use giant vesicles for substrate uptake studies in metabolically important tissues, we characterized giant vesicles isolated from heart, liver, skeletal muscle and adipose tissue. We investigated which cell types and which plasma membrane regions are involved in giant vesicle formation and we examined the presence of transporters for metabolic substrates. Analysis of giant vesicles with markers specific for distinct cell types and distinct domains of the plasma membrane reveals that the plasma membrane of parenchymal cells, but not endothelial cells, are the source of the vesicle membranes. In addition, plasma membrane regions enriched in caveolae and involved in docking of recycling vesicles from the endosomal compartment are retained in giant vesicles, indicating that KCl-induced alterations in recycling processes are involved in giant vesicle formation. Giant vesicles contain vesicular lumen consisting of the soluble constituents of the cytoplasm including, fatty-acid binding proteins. Furthermore, giant vesicles isolated from heart, liver, skeletal muscle and adipose tissue are similar in size (10-15 microm) and shape and do not contain subcellular organelles, providing the advantage that substrate fluxes in the different organs can be studied independently of the surface/volume ratio but most importantly in the absence of intracellular metabolism.

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Year:  2002        PMID: 12479577

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  52 in total

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Journal:  J Clin Invest       Date:  1988-09       Impact factor: 14.808

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Journal:  J Biol Chem       Date:  1998-07-03       Impact factor: 5.157

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  13 in total

1.  Long-chain fatty acid uptake by skeletal muscle is impaired in homozygous, but not heterozygous, heart-type-FABP null mice.

Authors:  J J F P Luiken; D P Y Koonen; W A Coumans; M M A L Pelsers; B Binas; A Bonen; J F C Glatz
Journal:  Lipids       Date:  2003-04       Impact factor: 1.880

2.  Nitric oxide can acutely modulate its biosynthesis through a negative feedback mechanism on L-arginine transport in cardiac myocytes.

Authors:  Jiaguo Zhou; David D Kim; R Daniel Peluffo
Journal:  Am J Physiol Cell Physiol       Date:  2010-05-26       Impact factor: 4.249

3.  Prolonged AMPK activation increases the expression of fatty acid transporters in cardiac myocytes and perfused hearts.

Authors:  Adrian Chabowski; Iman Momken; Susan L M Coort; Jorge Calles-Escandon; Narendra N Tandon; Jan F C Glatz; Joost J F P Luiken; Arend Bonen
Journal:  Mol Cell Biochem       Date:  2006-05-19       Impact factor: 3.396

4.  In obese Zucker rats, lipids accumulate in the heart despite normal mitochondrial content, morphology and long-chain fatty acid oxidation.

Authors:  Graham P Holloway; Laelie A Snook; Robert J Harris; Jan F C Glatz; Joost J F P Luiken; Arend Bonen
Journal:  J Physiol       Date:  2010-11-01       Impact factor: 5.182

5.  Munc18c provides stimulus-selective regulation of GLUT4 but not fatty acid transporter trafficking in skeletal muscle.

Authors:  Swati S Jain; Laelie A Snook; Jan F C Glatz; Joost J F P Luiken; Graham P Holloway; Debbie C Thurmond; Arend Bonen
Journal:  FEBS Lett       Date:  2012-06-08       Impact factor: 4.124

6.  Fatty acid binding protein facilitates sarcolemmal fatty acid transport but not mitochondrial oxidation in rat and human skeletal muscle.

Authors:  Graham P Holloway; Jamie Lally; James G Nickerson; Hakam Alkhateeb; Laelie A Snook; George J F Heigenhauser; Jorge Calles-Escandon; Jan F C Glatz; Joost J F P Luiken; Lawrence L Spriet; Arend Bonen
Journal:  J Physiol       Date:  2007-05-03       Impact factor: 5.182

7.  Greater transport efficiencies of the membrane fatty acid transporters FAT/CD36 and FATP4 compared with FABPpm and FATP1 and differential effects on fatty acid esterification and oxidation in rat skeletal muscle.

Authors:  James G Nickerson; Hakam Alkhateeb; Carley R Benton; James Lally; Jennifer Nickerson; Xiao-Xia Han; Meredith H Wilson; Swati S Jain; Laelie A Snook; Jan F C Glatz; Adrian Chabowski; Joost J F P Luiken; Arend Bonen
Journal:  J Biol Chem       Date:  2009-04-20       Impact factor: 5.157

8.  Differential effects of contraction and PPAR agonists on the expression of fatty acid transporters in rat skeletal muscle.

Authors:  Carley R Benton; Debby P Y Koonen; Jorge Calles-Escandon; Narendra N Tandon; Jan F C Glatz; Joost J F P Luiken; John J Heikkila; Arend Bonen
Journal:  J Physiol       Date:  2006-02-16       Impact factor: 5.182

Review 9.  Regulation of cardiac long-chain fatty acid and glucose uptake by translocation of substrate transporters.

Authors:  Joost J F P Luiken; Susan L M Coort; Debby P Y Koonen; Dick J van der Horst; Arend Bonen; Antonio Zorzano; Jan F C Glatz
Journal:  Pflugers Arch       Date:  2004-02-10       Impact factor: 3.657

10.  Subcellular immunolocalisation of fatty acid translocase (FAT)/CD36 in human type-1 and type-2 skeletal muscle fibres.

Authors:  Hans A Keizer; Gert Schaart; Narenda N Tandon; Jan F C Glatz; Joost J F P Luiken
Journal:  Histochem Cell Biol       Date:  2004-01-23       Impact factor: 4.304

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