Regulation of 25‐hydroxyvitamin D‐1‐hydroxylase and 24‐hydroxylase in keratinocytes by PTH and FGF23
- 1 August 2018
- journal article
- research article
- Published by Wiley in Experimental Dermatology
- Vol. 27 (11) , 1201-1209
Abstract
Renal 25‐hydroxyvitamin D‐1α‐hydroxylase (1αOHase, CYP27B1) and 24‐hydroxylase (24OHase, CYP24A1) are tightly regulated. However, little is known about the regulation of 1α(OH)ase and 24(OH)ase in extrarenal tissue such as the epidermis. This study was to determine the roles of parathyroid hormone (PTH) and fibroblast growth factor 23 (FGF 23) in the regulation of 1α(OH)ase and 24(OH)ase in epidermal keratinocytes as well as epidermal keratinocyte proliferation and differentiation. The results showed that PTH increased the protein level of 1α(OH)ase in human epidermal keratinocyte cell line HaCaT, but had no effect on the level of 24(OH)ase. The effect of PTH on 1α(OH)ase was blocked by the PKC inhibitor. Treatment with FGF23 decreased mRNA and protein levels of 1α(OH)ase and increased mRNA and protein levels of 24(OH)ase in HaCaT cells. The effect of FGF23 on 1α(OH)ase and 24(OH)ase was blocked by the mitogen‐activated protein kinase/extracellular regulated protein kinase (MAPK/ERK) inhibitor. In addition, treatment with PTH enhanced levels of differentiation markers including keratin 1, involucrin, loricrin, and filaggrin but reduced levels of BrdU incorporation in HaCaT cells. These effects were inhibited by the PKC inhibitor. FGF23 enhanced proliferation of HaCaT cells, but reduced levels of early differentiation markers including keratin 1 and involucrin and enhanced levels of the later differentiation markers including loricrin and filaggrin. These results suggest that PTH stimulates 1α(OH)ase expression and differentiation of HaCaT cells and inhibits proliferation via PKC. The data also suggest that FGF23 inhibits 1α(OH)ase expression and stimulates 24(OH)ase expression via MAPK/ERK. In addition, FGF23 enhances proliferation and late differentiation and inhibits early differentiation of HaCaT keratinocytes.Keywords
Funding Information
- National Natural Science Foundation of China (81072219, 81272973, 81471055, 81672646)
This publication has 71 references indexed in Scilit:
- Fibroblast growth factor 23 inhibits extrarenal synthesis of 1,25-dihydroxyvitamin D in human monocytesJournal of Bone and Mineral Research, 2012
- FGF23 neutralization improves chronic kidney disease–associated hyperparathyroidism yet increases mortalityJournal of Clinical Investigation, 2012
- Two Mechanisms Regulate Keratin K15 Expression In Keratinocytes: Role of PKC/AP-1 and FOXM1 Mediated SignallingPLOS ONE, 2012
- Fibroblast growth factor-23 and early decrements in kidney function: the Heart and Soul StudyNephrology Dialysis Transplantation, 2009
- Vitamin D-Directed Rheostatic Regulation of Monocyte Antibacterial ResponsesThe Journal of Immunology, 2009
- FGF-23–Klotho signaling stimulates proliferation and prevents vitamin D–induced apoptosisJournal of Cell Biology, 2008
- Fibroblast growth factor 23 impairs phosphorus and vitamin D metabolism in vivo and suppresses 25-hydroxyvitamin D-1α-hydroxylase expression in vitroAmerican Journal of Physiology-Renal Physiology, 2007
- Identification of a Novel Fibroblast Growth Factor, FGF-23, Preferentially Expressed in the Ventrolateral Thalamic Nucleus of the BrainBiochemical and Biophysical Research Communications, 2000
- Quantitative immunoelectron microscopic analysis of the localization and induction of 25-hydroxyvitamin D3 24-hydroxylase in rat kidney.Journal of Histochemistry & Cytochemistry, 1995
- Signal transduction in the onset of terminal keratinocyte differentiation induced by 1 α, 25-dihydroxyvitamin D3: Role of protein kinase C translocationBiochemical and Biophysical Research Communications, 1989