Expression of syntaxin 8 in visceral adipose tissue is increased in obese patients with type 2 diabetes and related to markers of insulin resistance and inflammation

Arch Med Res. 2015 Jan;46(1):47-53. doi: 10.1016/j.arcmed.2014.12.003. Epub 2014 Dec 15.

Abstract

Background and aims: Obesity is associated with increased adipose tissue inflammation as well as with the development of type 2 diabetes (T2D). Syntaxin 8 (STX8) is a protein required for the transport of endosomes. In this study we analyzed the relationship of STX8 with the presence of T2D in the context of obesity.

Methods: With this purpose, 21 subjects (seven lean [LN], eight obese normoglycemic [OB-NG] and six obese with type 2 diabetes [OB-T2D]) were included in the study. Gene and protein expression levels of STX8 and GLUT4 were analyzed in visceral adipose tissue (VAT).

Results: mRNA (p = 0.008) and protein (p <0.001) expression levels of STX8 were significantly increased in VAT of OB-T2D patients. Moreover, gene expression levels of SLC2A4 (GLUT4) were downregulated (p = 0.002) in VAT of obese patients. We found that STX8 was positively correlated (p <0.05) with fasting glucose concentrations, plasma glucose 2 h after an OGTT and C-reactive protein. Interestingly, the expression of STX8 was negatively correlated (p <0.05) with the expression of SLC2A4 in VAT.

Conclusions: Increased STX8 expression in VAT appears to be associated with the presence of T2D in obese patients through a mechanism that may involve GLUT4.

Keywords: GLUT4; Obesity; Syntaxin 8; Type 2 diabetes; Visceral adipose tissue.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biomarkers / metabolism
  • Blood Glucose / analysis
  • C-Reactive Protein / metabolism
  • Diabetes Mellitus, Type 2 / pathology*
  • Female
  • Gene Expression
  • Glucose Transporter Type 4 / biosynthesis*
  • Humans
  • Inflammation / immunology
  • Insulin Resistance / genetics
  • Intra-Abdominal Fat / metabolism*
  • Male
  • Middle Aged
  • Obesity / metabolism*
  • Qa-SNARE Proteins / biosynthesis*
  • RNA, Messenger / genetics

Substances

  • Biomarkers
  • Blood Glucose
  • Glucose Transporter Type 4
  • Qa-SNARE Proteins
  • RNA, Messenger
  • SLC2A4 protein, human
  • C-Reactive Protein