Literature DB >> 3045114

Reassessment of the translocation hypothesis by kinetic studies on hexose transport in isolated rat adipocytes.

K Suzuki1.   

Abstract

The effect of insulin and factors which have insulin-like activity on the kinetic parameters of 3-O-methyl-D-glucose (MeGlc) transport in rat adipocytes were assessed. Carrier-mediated uptake of MeGlc was estimated by the difference in the amounts of [14C]MeGlc and L-[3H]glucose taken up in cells under equilibrium exchange conditions at 37 degrees C. The Km and Vmax values in basal cells were 17.4 mM and 0.24 nmol/10(6) cells/s, respectively. Removal of endogenous adenosine by adenosine deaminase resulted in a 26% decrease in the basal rate due to a slight increase in the Km (19.6 mM) and a decrease in the Vmax value (0.20 nmol/10(6) cells/s). The maximum concentration (10 nM) of insulin decreased the Km to approximately one-half of the basal (7.1 mM) concomitant with an 8.5-fold increase in the Vmax value (2.04 nmol/10(6) cells/s). Submaximal concentrations (50 and 150 pM) of insulin, N6-phenylisopropyladenosine (1 microM), mechanical agitation of cells by centrifugal force (160 x g), low temperature (15 degrees C), 12-O-tetradecanoylphorbol-13-acetate (1 microM), and hydrogen peroxide (10 mM) all decreased the basal Km value to a range of 13.5-7.3 mM, concomitant with a 1.7-7.4-fold increase in the Vmax. A possible explanation for the alterations in the kinetic parameters may be that insulin and other factors cause the translocation of the mobile low-Km glucose transporters from an intracellular site to the cell surface, where the stationary high-Km transporters are located. Thus, when the Km and Vmax values of the hypothetical high-Km transporters were assumed to be 20 mM and 0.20 nmol/10(6) cells/s, respectively, and the Km of the low-Km transporters was assumed to be 7 mM, the theoretical Km decreased from 20 to 7.5 mM as the Vmax of the low-Km transporters increased from near 0 to 2.0 nmol/10(6) cells/s. The relation between empirical Km and Vmax values as affected by several agents and conditions followed closely the relation predicted by the above two-transporter model.

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Year:  1988        PMID: 3045114

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  7 in total

1.  A glucose transport protein expressed predominately in insulin-responsive tissues.

Authors:  M J Charron; F C Brosius; S L Alper; H F Lodish
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

Review 2.  Metabolic regulation of glucose transport.

Authors:  F Ismail-Beigi
Journal:  J Membr Biol       Date:  1993-07       Impact factor: 1.843

3.  Functional expression of mammalian glucose transporters in Xenopus laevis oocytes: evidence for cell-dependent insulin sensitivity.

Authors:  J C Vera; O M Rosen
Journal:  Mol Cell Biol       Date:  1989-10       Impact factor: 4.272

4.  Effect of osmolality and myo-inositol deprivation on the transport properties of myo-inositol in primary astrocyte cultures.

Authors:  R E Isaacks; A S Bender; C Y Kim; M D Norenberg
Journal:  Neurochem Res       Date:  1997-12       Impact factor: 3.996

5.  Enhancement of glucose transport in clone 9 cells by exposure to alkaline pH: studies on potential mechanisms.

Authors:  J Hakimian; F Ismail-Beigi
Journal:  J Membr Biol       Date:  1991-02       Impact factor: 1.843

6.  Effect of ammonia and methionine sulfoximine on myo-inositol transport in cultured astrocytes.

Authors:  R E Isaacks; A S Bender; C Y Kim; Y F Shi; M D Norenberg
Journal:  Neurochem Res       Date:  1999-01       Impact factor: 3.996

7.  Interleukin-3 facilitates glucose transport in a myeloid cell line by regulating the affinity of the glucose transporter for glucose: involvement of protein phosphorylation in transporter activation.

Authors:  M V Berridge; A S Tan
Journal:  Biochem J       Date:  1995-02-01       Impact factor: 3.857

  7 in total

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