Specific regulation of CYP27B1 and VDR in proximal versus distal renal cells

A Bajwa, MN Forster, A Maiti, BL Woolbright… - Archives of biochemistry …, 2008 - Elsevier
A Bajwa, MN Forster, A Maiti, BL Woolbright, MJ Beckman
Archives of biochemistry and biophysics, 2008Elsevier
In this study, we utilized murine renal proximal (MPCT-G) and distal (DKC-8) tubular
epithelial cell lines to compare the gene expressions and promoter activities of 1, 25 (OH)
2D3 receptor (VDR) and 25-hydroxyvitamin D-1α-hydroxylase (CYP27B1) in response to
50nM of parathyroid hormone (PTH) and changes in extracellular calcium (Ca2+)
concentration. In MPCT-G cells, VDR gene expression was suppressed by PTH, whereas
CYP27B1 gene expression was elevated in response to PTH. In DKC-8 cells, treatment of …
In this study, we utilized murine renal proximal (MPCT-G) and distal (DKC-8) tubular epithelial cell lines to compare the gene expressions and promoter activities of 1,25(OH)2D3 receptor (VDR) and 25-hydroxyvitamin D-1α-hydroxylase (CYP27B1) in response to 50nM of parathyroid hormone (PTH) and changes in extracellular calcium (Ca2+) concentration. In MPCT-G cells, VDR gene expression was suppressed by PTH, whereas CYP27B1 gene expression was elevated in response to PTH. In DKC-8 cells, treatment of PTH significantly increased the relative gene expression of VDR by 6.5-fold while CYP27B1 gene expression was unchanged. High Ca2+ exposure stimulated VDR gene expression and repressed CYP27B1 gene expression in both dose and time-dependent fashion in MPCT-G but not DKC-8 cells. The analysis of promoter activities and VDR protein levels corresponded with the gene expression data. We conclude that PTH-mediated decrease in VDR and increase in renal CYP27B1 is proximal cell-specific.
Elsevier