Transcriptional activation of apolipoprotein CIII expression by glucose may contribute to diabetic dyslipidemia

Arterioscler Thromb Vasc Biol. 2011 Mar;31(3):513-9. doi: 10.1161/ATVBAHA.110.220723. Epub 2010 Dec 23.

Abstract

Objective: Hypertriglyceridemia and fatty liver are common in patients with type 2 diabetes, but the factors connecting alterations in glucose metabolism with plasma and liver lipid metabolism remain unclear. Apolipoprotein CIII (apoCIII), a regulator of hepatic and plasma triglyceride metabolism, is elevated in type 2 diabetes. In this study, we analyzed whether apoCIII is affected by altered glucose metabolism.

Methods and results: Liver-specific insulin receptor-deficient mice display lower hepatic apoCIII mRNA levels than controls, suggesting that factors other than insulin regulate apoCIII in vivo. Glucose induces apoCIII transcription in primary rat hepatocytes and immortalized human hepatocytes via a mechanism involving the transcription factors carbohydrate response element-binding protein and hepatocyte nuclear factor-4α. ApoCIII induction by glucose is blunted by treatment with agonists of farnesoid X receptor and peroxisome proliferator-activated receptor-α but not liver X receptor, ie, nuclear receptors controlling triglyceride metabolism. Moreover, in obese humans, plasma apoCIII protein correlates more closely with plasma fasting glucose and glucose excursion after oral glucose load than with insulin.

Conclusions: Glucose induces apoCIII transcription, which may represent a mechanism linking hyperglycemia, hypertriglyceridemia, and cardiovascular disease in type 2 diabetes.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Animals
  • Apolipoprotein C-III / blood
  • Apolipoprotein C-III / genetics*
  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors / genetics
  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors / metabolism
  • Blood Glucose / metabolism
  • Cells, Cultured
  • Diabetes Complications / etiology*
  • Diabetes Complications / genetics
  • Diabetes Complications / metabolism
  • Diabetes Mellitus, Type 2 / complications*
  • Diabetes Mellitus, Type 2 / genetics
  • Diabetes Mellitus, Type 2 / metabolism
  • Dyslipidemias / etiology*
  • Dyslipidemias / genetics
  • Dyslipidemias / metabolism
  • Glucose / metabolism*
  • Heat-Shock Proteins / agonists
  • Heat-Shock Proteins / metabolism
  • Hepatocyte Nuclear Factor 4 / genetics
  • Hepatocyte Nuclear Factor 4 / metabolism
  • Hepatocytes / metabolism*
  • Humans
  • Insulin / blood
  • Liver X Receptors
  • Male
  • Mice
  • Mice, Knockout
  • Middle Aged
  • Obesity / blood
  • Orphan Nuclear Receptors / genetics
  • Orphan Nuclear Receptors / metabolism
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Promoter Regions, Genetic
  • RNA Interference
  • RNA, Messenger / metabolism
  • RNA-Binding Proteins / agonists
  • RNA-Binding Proteins / metabolism
  • Rats
  • Receptor, Insulin / deficiency
  • Receptor, Insulin / genetics
  • Receptors, Cytoplasmic and Nuclear / agonists
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Time Factors
  • Transcription Factors / agonists
  • Transcription Factors / metabolism
  • Transcriptional Activation*
  • Transfection
  • Up-Regulation

Substances

  • Apolipoprotein C-III
  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
  • Blood Glucose
  • HNF4A protein, human
  • Heat-Shock Proteins
  • Hepatocyte Nuclear Factor 4
  • Insulin
  • Liver X Receptors
  • MLXIPL protein, human
  • Mlxipl protein, rat
  • Orphan Nuclear Receptors
  • PPARGC1A protein, human
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Ppargc1a protein, rat
  • RNA, Messenger
  • RNA-Binding Proteins
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • farnesoid X-activated receptor
  • Receptor, Insulin
  • Glucose