Literature DB >> 1644862

Expression of glucose transporters (GLUT 1 and GLUT 4) in primary cultured rat adipocytes: differential evolution with time and chronic insulin effect.

E J Hajduch1, M C Guerre-Millo, I A Hainault, C M Guichard, M M Lavau.   

Abstract

We previously reported that in cultured adipose cell lines insulin increased selectively the expression of Glut 1, in contrast to in vivo regulation where variations in insulinemia have been shown to affect only GLUT 4. We have addressed here the question of the long-term regulation of GLUT 1 and GLUT 4 in fat cells by using primary cultures of rat adipocytes. Epididymal fat cells were isolated by collagenase and cultured 4 days in DMEM supplemented with BSA 1%, FCS 1%, and glucose 10 mM. GLUT 1 and GLUT 4 proteins were assessed in total cellular membranes by Western blotting, using specific antibodies against their respective C-terminal peptides. GLUT 1 steadily increased over culture time to reach at day 3, a level 3-fold higher than the initial value. In contrast, GLUT 4 decreased sharply and stabilized at day 3, at 30% of the initial value. The changes in GLUT 1 and GLUT 4 mRNAs with culture time were parallel to changes in the corresponding proteins, suggesting a pre-translational level of regulation. The expression of the lipogenic enzyme, fatty acid synthetase (FAS), highly expressed in fat cell, decreased over time following a pattern closely parallel to that of GLUT 4. Chronic exposure to insulin added at day 2 had no effect on GLUT 4 expression but increased the expression of GLUT 1 and FAS by 70% and 36%, respectively. Glucose consumption was stable over 4 days of culture, while lactate production increased from 24 to 36% of glucose utilization, in agreement with the loss in FAS. Glucose consumption increased only slightly with insulin (+160%), in good keeping with the low levels of expression of both GLUT 4 and FAS in these cultured cells. These data indicate that culture alters oppositely the expression of GLUT 1 and GLUT 4 in rat adipocytes and suggest that factor(s) other than insulin predominate in their regulation in vivo.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1644862     DOI: 10.1002/jcb.240490307

Source DB:  PubMed          Journal:  J Cell Biochem        ISSN: 0730-2312            Impact factor:   4.429


  6 in total

1.  Thiazolidinediones repress ob gene expression in rodents via activation of peroxisome proliferator-activated receptor gamma.

Authors:  P De Vos; A M Lefebvre; S G Miller; M Guerre-Millo; K Wong; R Saladin; L G Hamann; B Staels; M R Briggs; J Auwerx
Journal:  J Clin Invest       Date:  1996-08-15       Impact factor: 14.808

2.  The GLUT3 glucose transporter is the predominant isoform in primary cultured neurons: assessment by biosynthetic and photoaffinity labelling.

Authors:  F Maher; I A Simpson
Journal:  Biochem J       Date:  1994-07-15       Impact factor: 3.857

3.  The adipocyte specific transcription factor C/EBPalpha modulates human ob gene expression.

Authors:  S G Miller; P De Vos; M Guerre-Millo; K Wong; T Hermann; B Staels; M R Briggs; J Auwerx
Journal:  Proc Natl Acad Sci U S A       Date:  1996-05-28       Impact factor: 11.205

4.  IRS1-independent defects define major nodes of insulin resistance.

Authors:  Kyle L Hoehn; Cordula Hohnen-Behrens; Anna Cederberg; Lindsay E Wu; Nigel Turner; Tomoyuki Yuasa; Yousuke Ebina; David E James
Journal:  Cell Metab       Date:  2008-05       Impact factor: 27.287

5.  Fructose transport and metabolism in adipose tissue of Zucker rats: diminished GLUT5 activity during obesity and insulin resistance.

Authors:  Gary J Litherland; Eric Hajduch; Gwyn W Gould; Harinder S Hundal
Journal:  Mol Cell Biochem       Date:  2004-06       Impact factor: 3.396

6.  Extra fructose in the growth medium fuels lipogenesis of adipocytes.

Authors:  Armin Robubi; Klaus R Huber; Walter Krugluger
Journal:  J Obes       Date:  2014-02-19
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.