Expression study of GLUT4 translocation-related genes in a porcine pre-diabetic model
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  • 作者:Thea Kristensen ; Merete Fredholm ; Susanna Cirera
  • 刊名:Mammalian Genome
  • 出版年:2015
  • 出版时间:December 2015
  • 年:2015
  • 卷:26
  • 期:11-12
  • 页码:650-657
  • 全文大小:870 KB
  • 参考文献:Andersen CL, Jensen JL, ?rntoft TF (2004) Normalization of real-time quantitative reverse transcription-PCR data: a model-based variance estimation approach to identify genes suited for normalization applied to bladder and colon cancer data sets normalization of real-time quantitative reverse. Cancer Res 64:5245-250. doi:10.-158/-008-5472.?CAN-04-0496 CrossRef PubMed
    Bianchin F, Kaaks R, Vainio H (2002) Overweight, obesity, and cancer risk. Lancet Oncol 3(9):565-74CrossRef
    Bouzakri K, Ribaux P, Alejandra T, Parnaud G, Rickenbach K, Halban PA (2008) Rab GTPase-activating protein AS160 is a major downstream effector of protein kinase B/Akt signaling in pancreatic Β-cells. Apoptosis 57:1195-204. doi:10.-337/?db07-1469.?P.?R
    Butler AE, Juliette J, Bonner-Weir S, Ritzel R, Rizza RA, Butler PC (2003) Β-cell deficit and increased Β-cell apoptosis in humans with type 2. Diabetes 52:102-10CrossRef PubMed
    Cirera S (2013) Highly efficient method for isolation of total RNA from adipose tissue. BMC Res Notes 6:472. doi:10.-186/-756-0500-6-472 PubMedCentral CrossRef PubMed
    De Meyts P, Palsgaard J, Sajid W, Theede AM, Aladdin H (2004) Structural biology of insulin and IGF-1 receptors. Novartis Found Symp 262:160-71. doi:10.-038/?nrd917 (discussion 171-6, 265-8) CrossRef PubMed
    Eguez L, Lee A, Chavez JA, Miinea CP, Kane S, Lienhard GE, McGraw TE (2005) Full intracellular retention of GLUT4 requires AS160 Rab GTPase activating protein. Cell Metab 2:263-72. doi:10.-016/?j.?cmet.-005.-9.-05 CrossRef PubMed
    Hoehn KL, Hohnen-Behrens C, Cederberg A, Wu LE, Turner N, Yuasa T, Ebina Y, James DE (2008) IRS1-independent defects define major nodes of insulin resistance. Cell Metab 7:421-33. doi:10.-016/?j.?cmet.-008.-4.-05 PubMedCentral CrossRef PubMed
    Hribal M, Perego L, Lovari S, Andreozzi F, Menghini R, Perego C, Finzi G et al (2003) Chronic hyperglycemia impairs insulin secretion by affecting insulin receptor expression, splicing, and signaling in RIN beta cell line and human islets of langerhans. FASEB J 17:1340-342. doi:10.-096/?fj.-2-0685fje PubMed
    Imamura M, Maeda S (2011) Genetics of Type 2 diabetes: the GWAS era and future perspectives [review]. Endocr J 58(9):723-39. doi:10.-507/?endocrj.?EJ11-0113 CrossRef PubMed
    Kogelman LJA, Kadarmideen HN, Mark T, Karlskov-Mortensen P, Bruun CS, Cirera S, Jacobsen MJ, J?rgensen CB, Fredholm M (2013) An F2 pig resource population as a model for genetic studies of obesity and obesity-related diseases in humans: design and genetic parameters. Front Genet 4:1-4. doi:10.-389/?fgene.-013.-0029 CrossRef
    Kulkarni RN, Brüning JC, Winnay JN, Postic C, Magnuson MA, Kahn CR (1999) Tissue-specific knockout of the insulin receptor in pancreatic Β cells creates an insulin secretory defect similar to that in type 2 diabetes. Cell 96:329-39. doi:10.-016/?S0092-8674(00)80546-2 CrossRef PubMed
    Larance M, Ramm G, St?ckli J, Van Dam E, Winata S, Wasinger V, Simpson F et al (2005) Characterization of the role of the Rab GTPase-activating protein AS160 in insulin-regulated GLUT4 trafficking. J Biol Chem 280:37803-7813. doi:10.-074/?jbc.?M503897200 CrossRef PubMed
    Leibiger B, Leibiger I, Moede T, Kemper S, Kulkarni R, Ronald Kahn C, Vargas L, Berggren P (2001) Selective insulin signaling through A and B insulin receptors regulates transcription of insulin and glucokinase genes in pancreatic beta Cells. Mol Cell 7:559-70. doi:10.-016/?S1097-2765(01)00203-9 CrossRef PubMed
    Minokoshi Y, Ronald Kahn C, Kahn B (2003) Tissue-specific ablation of the GLUT4 glucose transporter or the insulin receptor challenges assumptions about insulin action and glucose homeostasis. J Biol Chem 278:33609-3612. doi:10.-074/?jbc.?R300019200 CrossRef PubMed
    Moltke I, Grarup N, J?rgensen M, Bjerregaard P, Treebak J, Fumagalli M, Korneliussen T et al (2014) A common greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes. Nature. doi:10.-038/?nature13425 PubMedCentral
    Nygard A-B, J?rgensen C, Cirera S, Fredholm M (2007) Selection of reference genes for gene expression studies in pig tissues using SYBR green qPCR. BMC Mol Biol 8(January):67. doi:10.-186/-471-2199-8-67 PubMedCentral CrossRef PubMed
    Oliveira J, Rebuffat S, Gasa R, Gomis R (2014) Targeting type 2 diabetes: lessons from a Knockout model of insulin receptor substrate 2. NRP Res Press 620(June):613-20
    Pant SD, Karlskov-Mortensen P, Jacobsen MJ, Cirera S, Kogelman LJA, Bruun CS, Mark T, J?rgensen CB, Grarup N, Appel EVR, Galjatovic EAA, Hansen T, Pedersen O, Guerin M, Huby T, Lesnik P, Meuwissen THE, Kadarmideen HN, Fredholm M (in press) Comparative analyses of QTLs influencing obesity and metabolic phenotypes in pigs and humans. PLoS ONE
    Postic C, Leturque A, Rencurel F, Printz R, Forest C, Granner D, Girard J (1993) The effects of hyperinsulinemia and hyperglycemia on GLUT4 and hexokinase II mRNA and protein in rat skeletal muscle and
  • 作者单位:Thea Kristensen (1)
    Merete Fredholm (1)
    Susanna Cirera (1)

    1. Department of Veterinary Clinical and Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, 1870, Frederiksberg C, Denmark
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Life Sciences
    Cell Biology
    Anatomy
    Zoology
  • 出版者:Springer New York
  • ISSN:1432-1777
文摘
Obesity is a world-wide exponentially growing health problem that increases the risk of co-morbidities including metabolic syndrome, pre-diabetes, Type 2 Diabetes Mellitus (T2DM), and cancer. These co-morbidities are all complex conditions constituting a big challenge when searching for susceptibility genes. Identification of relevant genes, which could contribute to an earlier identification of individuals prone to develop diabetes, is urgently needed as many long-term complications can be avoided by preventive measures. Pre-diabetes is mainly associated with hyperglycemia; thus studying this phenotype might provide knowledge on relevant genes implicated in molecular mechanisms underlying pre-diabetes, and contributing to the development of T2DM. In the present study, two groups of pigs with high (HGG, N = 6) and low (NGG, N = 6) fasting plasma glucose level respectively were selected from a large pig population. Transcriptional levels of seven genes involved in the glucose transporter 4 (GLUT4) translocation pathway were studied by quantitative real-time PCR (qPCR) in diabetes relevant tissues (pancreas, adipose tissue, skeletal muscle, liver and kidney). Three of the genes, TBC (Tre-2, BUB2, CDC16) 1 Domain Family Member 4 (TBC1D4), insulin receptor and GLUT4 showed altered expression in some of the tissues. The expression pattern observed is in agreement with what has previously been reported in pre-diabetic humans confirming the pre-diabetic status of our pigs. Moreover, a novel isoform of TBC1D4 was detected by Western blotting using protein extracted from pancreas. The expression level of this novel isoform was further verified by qPCR in all tissues, showing the highest expression in the pancreas. Electronic supplementary materialThe online version of this article (doi:10.-007/?s00335-015-9601-z) contains supplementary material, which is available to authorized users.

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