Monocytes from type 2 diabetic patients have a pro-inflammatory profile. 1,25-Dihydroxyvitamin D(3) works as anti-inflammatory

Diabetes Res Clin Pract. 2007 Jul;77(1):47-57. doi: 10.1016/j.diabres.2006.10.007. Epub 2006 Nov 16.

Abstract

The exact factors contributing to the pathogenesis of type 2 diabetes remain elusive. Lately, it was suggested that inflammation and activation of the innate immune system could be linked to type 2 diabetes pathogenesis and also to the development of common diabetic complications, mainly atherosclerosis. The aim of this study was to investigate the role of monocytes in this sub-clinical inflammatory state and test 1,25-dihydroxyvitamin D(3), the active form of Vitamin D, as an anti-inflammatory agent. For this purpose, monocytes from type 2 diabetic patients were compared to monocytes from healthy controls and type 1 diabetic patients. The expression profile of inflammatory markers in freshly isolated and immune-stimulated monocytes was measured by quantitative real-time RT-PCR. Type 2 diabetic patients showed significantly higher expression levels of TNF-alpha, IL-6, IL-1, IL-8, COX-2, ICAM-1 and B7-1 compared to controls and type 1 diabetic patients. 1,25-Dihydroxyvitamin D(3) was able to down-regulate the expression of TNF-alpha, IL-6, IL-1, and IL-8, confirming its immunomodulatory properties. From these data we concluded that monocytes from type 2 diabetic patients have a pro-inflammatory profile. In addition, 1,25-dihydroxyvitamin D(3) was able to modulate inflammation in these monocytes.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged, 80 and over
  • Anti-Inflammatory Agents / pharmacology*
  • B7-1 Antigen / biosynthesis
  • Calcitriol / pharmacology*
  • Cyclooxygenase 2 / biosynthesis
  • Diabetes Mellitus, Type 1 / blood
  • Diabetes Mellitus, Type 2 / blood*
  • Down-Regulation
  • Female
  • Humans
  • Inflammation / physiopathology*
  • Intercellular Adhesion Molecule-1 / biosynthesis
  • Interferon-gamma / pharmacology
  • Interleukins / biosynthesis
  • Male
  • Middle Aged
  • Monocytes / drug effects
  • Monocytes / physiology*
  • Tumor Necrosis Factor-alpha / biosynthesis

Substances

  • Anti-Inflammatory Agents
  • B7-1 Antigen
  • Interleukins
  • Tumor Necrosis Factor-alpha
  • Intercellular Adhesion Molecule-1
  • Interferon-gamma
  • Cyclooxygenase 2
  • Calcitriol