Literature DB >> 6540601

Partial characterization of the glucose transport activity in the Golgi-rich fraction of fat cells.

M M Smith, F W Robinson, T Watanabe, T Kono.   

Abstract

The glucose transport activity solubilized from the basal and plus insulin forms of the Golgi-rich fraction of adipocytes was partially characterized, and the results were compared with those of the activity obtained from the plus insulin form of the plasma membrane-rich fraction. The transport activity was determined in a cell-free, reconstituted, system. Prior to reconstitution, the activities in the three preparations were all (a) stable at 0 degrees C for at least 4 h, but not at 37 degrees C or above; (b) most stable at pH 7-9, and (c) less stable in Tes than in Tris buffer. After reconstitution, the three activities were all (d) stable at 0 degrees C, (e) most active at pH 5.5, (f) mildly stimulated by divalent cations, (g) unaffected by insulin or 1 mM of several SH-blocking agents, (h) inhibited by heavy metal ions, 10-100 mM of monovalent salts, organic solvents, several sugar isomers, and specific sugar-transport inhibitors. The rates of D-glucose uptake by the three liposome preparations were all inhibited more strongly by 2-deoxy-D-glucose or 3-O-methyl-D-glucose than by D-glucose. These data indicate that the general properties of the glucose transport activity in the Golgi-rich fraction are similar to those of the activity in the plasma membrane-rich fraction.

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Year:  1984        PMID: 6540601     DOI: 10.1016/0005-2736(84)90162-7

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  7 in total

1.  Possible role for gp160 in constitutive but not insulin-stimulated GLUT4 trafficking: dissociation of gp160 and GLUT4 localization.

Authors:  A Filippis; S Clark; J Proietto
Journal:  Biochem J       Date:  1998-02-15       Impact factor: 3.857

2.  Insulin-responsive tissues contain the core complex protein SNAP-25 (synaptosomal-associated protein 25) A and B isoforms in addition to syntaxin 4 and synaptobrevins 1 and 2.

Authors:  M N Jagadish; C S Fernandez; D R Hewish; S L Macaulay; K H Gough; J Grusovin; A Verkuylen; L Cosgrove; A Alafaci; M J Frenkel; C W Ward
Journal:  Biochem J       Date:  1996-08-01       Impact factor: 3.857

3.  Enhancement of glucose transport by insulin at 37 degrees C in rat adipocytes is accounted for by increased Vmax.

Authors:  Y Okuno; J Gliemann
Journal:  Diabetologia       Date:  1987-06       Impact factor: 10.122

4.  Mechanism for enhanced glucose transport response to insulin in adipose cells from chronically hyperinsulinemic rats. Increased translocation of glucose transporters from an enlarged intracellular pool.

Authors:  B B Kahn; E S Horton; S W Cushman
Journal:  J Clin Invest       Date:  1987-03       Impact factor: 14.808

5.  Functional studies in 3T3L1 cells support a role for SNARE proteins in insulin stimulation of GLUT4 translocation.

Authors:  S L Macaulay; D R Hewish; K H Gough; V Stoichevska; S F MacPherson; M Jagadish; C W Ward
Journal:  Biochem J       Date:  1997-05-15       Impact factor: 3.857

6.  Isoproterenol inhibits cyclic AMP-mediated but not insulin-mediated translocation of the GLUT4 glucose transporter isoform.

Authors:  S L Macaulay; A S Kelada; J Proietto
Journal:  Mol Cell Biochem       Date:  1994-12-07       Impact factor: 3.396

7.  Divergent mechanisms for the insulin resistant and hyperresponsive glucose transport in adipose cells from fasted and refed rats. Alterations in both glucose transporter number and intrinsic activity.

Authors:  B B Kahn; I A Simpson; S W Cushman
Journal:  J Clin Invest       Date:  1988-08       Impact factor: 14.808

  7 in total

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