Gene expression profiles in peripheral blood mononuclear cells reflect the pathophysiology of type 2 diabetes

Biochem Biophys Res Commun. 2007 Sep 21;361(2):379-84. doi: 10.1016/j.bbrc.2007.07.006. Epub 2007 Jul 16.


We hypothesized that systemically circulating peripheral blood mononuclear cells (PBMCs) reflect the pathophysiology of type 2 diabetes. PBMCs were obtained from 18 patients with type 2 diabetes and 16 non-diabetic subjects. The expression of genes in the PBMCs was analyzed by using a DNA chip followed by statistical analysis for specific gene sets for biological categories. The only gene set coordinately up-regulated by the existence of diabetes and down-regulated by glycemic control consisted of 48 genes involved in the c-Jun N-terminal kinase (JNK) pathway. In contrast, the only gene set coordinately down-regulated by the existence of diabetes, but not altered by glycemic control consisted of 92 genes involved in the mitochondrial oxidative phosphorylation (OXPHOS) pathway. Our findings suggest that genes involved in the JNK and OXPHOS pathways of PBMCs may be surrogate transcriptional markers for hyperglycemia-induced oxidative stress and morbidity of type 2 diabetes, respectively.

MeSH terms

  • Adult
  • Diabetes Mellitus, Type 2 / epidemiology
  • Diabetes Mellitus, Type 2 / genetics*
  • Female
  • Gene Expression Profiling*
  • Humans
  • Hyperglycemia / enzymology
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • Japan / epidemiology
  • Leukocytes, Mononuclear / metabolism*
  • Male
  • Oxidative Phosphorylation


  • JNK Mitogen-Activated Protein Kinases