Flow cytometry detection of vitamin D receptor changes during vitamin D treatment in Crohn's disease. (5th May 2015)

• Record Type: Journal Article
• Authors: Bendix, M.; Dige, A.; Deleuran, B.; Dahlerup, J. F.; Jørgensen, S. P.; Bartels, L. E.; Husted, L. B.; Harsløf, T.; Langdahl, B.; Agnholt, J.
• Is Part Of: Clinical and experimental immunology. Volume 181:Number 1(2015:Jul.)
• Page Start: 19
• Page End: 28
• Publication Date: 2015-05-05
• Subjects: Crohn's disease -- flow cytometry -- T cells -- VDR -- vitamin D; Immunopathology -- Periodicals; 616.079
• DOI: 10.1111/cei.12613
• Languages: English
• ISSNs: 0009-9104

Abstract

Summary: Crohn's disease (CD) is a chronic inflammatory disease associated with a dysregulated T cell response towards intestinal microflora. Vitamin D has immune modulatory effects on T cells through the nuclear vitamin D receptor (VDR) in vitro . It is unclear how oral vitamin D treatment affects VDR expression. The aim of this study was to establish a flow cytometry protocol, including nuclear and cytoplasmic VDR expression, and to investigate the effects of vitamin D treatment on T cell VDR expression in CD patients. The flow cytometry protocol for VDR staining was developed using the human acute monocytic leukaemia cell line (THP‐1). The protocol was evaluated in anti‐CD3/CD28‐stimulated peripheral blood mononuclear cells (PBMCs) from vitamin D3‐ ( n = 9) and placebo‐treated ( n = 9) CD patients. Anti‐VDR‐stained PBMCs were examined by flow cytometry, and their cytokine production was determined by cytokine bead array. VDR, CYP27B1 and RXRα mRNA expression levels in CD4 + T cells were measured by quantitative reverse transcriptase polymerase chain reaction. The flow cytometry protocol enabled detection of cytoplasmic and nuclear VDR expression. The results were confirmed by confocal microscopy and supported by correlation with VDR mRNA expression. VDR expression in CD4 + T cells increased following stimulation. This VDR up‐regulation was inhibited with 30% by vitamin D treatment compared to placebo in CD patients ( P = 0·027). VDR expression was correlated with in‐vitro interferon‐γ production in stimulated PBMCs ( P = 0·01). Flow cytometry is a useful method with which to measure intracellular VDR expression. Vitamin D treatment in CD patients reduces T cell receptor‐mediated VDR up‐regulation.