Regulation of 25‐hydroxyvitamin D‐1‐hydroxylase and 24‐hydroxylase in keratinocytes by PTH and FGF23. Issue 11 (5th September 2018)

• Record Type: Journal Article
• Authors: Wu, Wenlin; Fan, Hong; Jiang, Yi; Liao, Liyan; Li, Lusha; Zhao, Juan; Zhang, Huiling; Shrestha, Chandrama; Xie, Zhongjian
• Is Part Of: Experimental dermatology. Volume 27:Issue 11(2018)
• Page Start: 1201
• Page End: 1209
• Publication Date: 2018-09-05
• Subjects: 1, 25(OH)2D -- fibroblast growth factor 23 -- keratinocytes -- proliferation -- parathyroid hormone; Dermatology -- Periodicals; 616.5
• DOI: 10.1111/exd.13760
• Languages: English
• ISSNs: 0906-6705

Abstract

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.