The Effect of Caffeine on Calcitriol-Inducible Vitamin D Receptor-Controlled Gene Expression in Intestinal and Osteoblastic Cells.
Ondřej ŽenataAdéla MarcalíkováRadim VrzalPublished in: Calcified tissue international (2019)
Some epidemiological studies suggested caffeine consumption as the cause for bone mineral density loss. Certain genes involved in this process are regulated by vitamin D receptor (VDR). Therefore, we investigated if caffeine can affect inducible expression of VDR-regulated genes, some of them being involved in bone mineralization process. By employing reporter gene assay, polymerase chain reaction, and western blotting, we monitored the VDR activity and expression in cell cultures of intestinal (LS180), osteosarcoma (HOS), and normal human osteoblasts in vitro. While caffeine stimulated calcitriol-inducible VDR-dependent nanoluciferase activity in stable reporter cell line IZ-VDRE (derived from LS180), it rather modulated mRNA levels of target genes, like CYP24A1, BGLAP, SPP1, and TNSF11 in LS180 and HOS cells. However, caffeine significantly decreased calcitriol-inducible CYP24A1, TNSF11, and SPP1 transcripts in osteoblasts. This decrease had non-linear U-shaped profile. Our in vitro data demonstrate biphasic action of caffeine on the expression of certain calcitriol-inducible VDR-regulated genes in normal human osteoblasts.
Keyphrases
- bone mineral density
- poor prognosis
- genome wide
- gene expression
- induced apoptosis
- endothelial cells
- genome wide identification
- postmenopausal women
- cell cycle arrest
- binding protein
- transcription factor
- dna methylation
- body composition
- crispr cas
- bioinformatics analysis
- single cell
- genome wide analysis
- high throughput
- stem cells
- oxidative stress
- cell death
- electronic health record
- endoplasmic reticulum stress
- south africa
- cell proliferation
- deep learning
- single molecule
- atomic force microscopy