Literature DB >> 12700047

Regulation of GLUT4 expression in vivo and in vitro.

Ann Louise Olson1, John B Knight.   

Abstract

The GLUT4 gene is subject to complex tissue-specific and metabolic regulation that has a profound impact on insulin-mediated glucose disposal. The regulation of this gene is of special clinical interest because insulin-mediated glucose homeostasis is highly sensitive to the levels of GLUT4 protein in muscle and adipose tissue. For this reason, the mechanisms of regulated expression of the GLUT4 gene have been intensively studied over the past decade. Understanding the transcriptional mechanisms that underlie the regulated expression of this highly differentiated gene have been slow to emerge, due to the paucity of suitable model systems available for detailed investigation. The development of transgenic mouse models to understand the mechanisms of transcriptional regulation has greatly enhanced our understanding of this gene. Information gained about the regulation of the GLUT4 gene has provided insight into mechanisms by which complex gene regulation occurs through a small number of cis-acting regulatory elements.

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Year:  2003        PMID: 12700047     DOI: 10.2741/1072

Source DB:  PubMed          Journal:  Front Biosci        ISSN: 1093-4715


  9 in total

1.  Repression of GLUT4 expression by the endoplasmic reticulum stress response in 3T3-L1 adipocytes.

Authors:  Ryan S Miller; Daniel Diaczok; David W Cooke
Journal:  Biochem Biophys Res Commun       Date:  2007-08-09       Impact factor: 3.575

Review 2.  Hepatitis C virus infection and insulin resistance.

Authors:  Sandip K Bose; Ranjit Ray
Journal:  World J Diabetes       Date:  2014-02-15

3.  Chronic inhibition of the mTORC1/S6K1 pathway increases insulin-induced PI3K activity but inhibits Akt2 and glucose transport stimulation in 3T3-L1 adipocytes.

Authors:  Alain Veilleux; Vanessa P Houde; Kerstin Bellmann; André Marette
Journal:  Mol Endocrinol       Date:  2010-03-04

4.  Cerebellar neurons possess a vesicular compartment structurally and functionally similar to Glut4-storage vesicles from peripheral insulin-sensitive tissues.

Authors:  Kyriaki Bakirtzi; Gabriel Belfort; Ignacio Lopez-Coviella; Darshini Kuruppu; Lei Cao; E Dale Abel; Anna-Liisa Brownell; Konstantin V Kandror
Journal:  J Neurosci       Date:  2009-04-22       Impact factor: 6.167

Review 5.  Vitamin C transporters.

Authors:  C I Rivas; F A Zúñiga; A Salas-Burgos; L Mardones; V Ormazabal; J C Vera
Journal:  J Physiol Biochem       Date:  2008-12       Impact factor: 4.158

6.  Reversible insulin resistance helps Bactrian camels survive fasting.

Authors:  Fucheng Guo; Rendalai Si; Quanyun Li; Le Hai; Li Yi; Jing He; Liang Ming; Rimutu Ji
Journal:  Sci Rep       Date:  2021-09-22       Impact factor: 4.379

7.  Acute inhibition of fatty acid import inhibits GLUT4 transcription in adipose tissue, but not skeletal or cardiac muscle tissue, partly through liver X receptor (LXR) signaling.

Authors:  Beth A Griesel; Juston Weems; Robert A Russell; E Dale Abel; Kenneth Humphries; Ann Louise Olson
Journal:  Diabetes       Date:  2010-01-26       Impact factor: 9.461

Review 8.  Regulation of GLUT4 and Insulin-Dependent Glucose Flux.

Authors:  Ann Louise Olson
Journal:  ISRN Mol Biol       Date:  2012-10-17

Review 9.  Hepatitis C virus infection in chronic kidney disease: paradigm shift in management.

Authors:  So Mi Kim; Il Han Song
Journal:  Korean J Intern Med       Date:  2018-06-28       Impact factor: 2.884

  9 in total

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