[Effects of NYGGF4 gene over-expression on the insulin sensitivity and secretory function of adipocytes]

Zhongguo Dang Dai Er Ke Za Zhi. 2009 Oct;11(10):846-9.
[Article in Chinese]

Abstract

Objective: To study the effect of a new obesity-related gene NYGGF4 on the insulin sensitivity and secretory function of adipocytes.

Methods: 3T3-L1 preadipocytes transfected with either an empty expression vector (pcDNA3.1; control group) or an NYGGF4 expression vector (NYGGF4-pcDNA3.1) were cultured in vitro and differentiated into the matured adipocytes with the standard insulin plus dexamethasone plus 3-isobutyl-methylxanthine (MDI) induction cocktail. 2-deoxy-D-[3H] glucose uptake was determined by liquid scintillation counting. Western blot was performed to detect the protein content and translocation of glucose transporter 4 (GLUT4). The supernatant concentrations of TNF-alpha, IL-6, adiponectin and resistin were measured using ELISA.

Results: NYGGF4 over-expression in 3T3-L1 adipocytes reduced insulin-stimulated glucose uptake. NYGGF4 over-expression impaired insulin-stimulated GLUT4 translocation without affecting the total protein content of GLUT4. The concentrations of TNF-alpha, IL-6, adiponectin and resistin in the culture medium of 3T3-L1 transfected with NYGGF4 were not significantly different from those in the control group.

Conclusions: NYGGF4 over-expression impairs the insulin sensitivity of 3T3-L1 adipocytes through decreasing GLUT4 translocation and had no effects on the secretory function of adipocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / drug effects*
  • Adipocytes / metabolism
  • Adiponectin / metabolism
  • Animals
  • Carrier Proteins / genetics
  • Carrier Proteins / physiology*
  • Glucose / metabolism
  • Glucose Transporter Type 4 / analysis
  • Glucose Transporter Type 4 / metabolism
  • Insulin / pharmacology*
  • Interleukin-6 / metabolism
  • Mice
  • Resistin / analysis
  • Transfection
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Adiponectin
  • Carrier Proteins
  • Glucose Transporter Type 4
  • Insulin
  • Interleukin-6
  • PID1 protein, human
  • Resistin
  • Tumor Necrosis Factor-alpha
  • Glucose