Regulation of 1, 25-dihydroxyvitamin d production in human keratinocytes by interferon-γ

DD Bikle, S PILLAI, E GEE, M HINCENBERGS - Endocrinology, 1989 - academic.oup.com
DD Bikle, S PILLAI, E GEE, M HINCENBERGS
Endocrinology, 1989academic.oup.com
Interferon-γ (IFNγ) and 1, 25-dihydroxyvitamin D [1, 25-(OH) 2D] each have potent
antiproliferative and prodifferentiating effects on keratinocytes. Since keratinocytes produce
1, 25-(OH) 2D, we explored the possibility that IFNγ acted on keratinocytes in part by
regulating 1, 25-(OH) 2D production. We cultured human neonatal foreskin keratinocytes for
various periods of time in the presence of various concentrations of IFNγ before assessing
their ability to produce 1, 25-(OH) 2D. The production of 1, 25-(OH) 2D by preconfluent …
Interferon-γ (IFNγ) and 1,25-dihydroxyvitamin D [1,25-(OH)2D] each have potent antiproliferative and prodifferentiating effects on keratinocytes. Since keratinocytes produce 1,25-(OH)2D, we explored the possibility that IFNγ acted on keratinocytes in part by regulating 1,25-(OH)2D production. We cultured human neonatal foreskin keratinocytes for various periods of time in the presence of various concentrations of IFNγ before assessing their ability to produce 1,25-(OH)2D. The production of 1,25-(OH)2D by preconfluent keratinocytes grown in the presence of serum (which retards differentiation) was stimulated by 1.8 nM IFNγ. Postconfluent keratinocytes did not respond to 1.8 nM IFNγ. The production of 1,25-(OH)2D by keratinocytes grown in serum-free medium was maximally stimulated by 0.006 nM IFNγ and inhibited at concentrations greater than 0.06 nM. Keratinocytes grown in 0.1 mM calcium serumfree medium (which prevents differentiation) were more sensitive to both the stimulatory and inhibitory effects of IFNγ than keratinocytes grown in 1.2 mM calcium serum-free medium (which permits differentiation). The stimulatory effect of IFNγ on 1,25-(OH)2D production was maximal after 2 days of incubation. Incubations longer than 2 days showed increasingly less stimulation at the low IFNγ concentrations and increasingly greater inhibition at the higher IFNγ concentrations. The inhibitory effects of IFNγ on 1,25-(OH)2D production paralleled the inhibitory effects of IFNγ on cell growth. Thus, IFNγ does regulate 1,25-(OH)2D production by keratinocytes. However, this regulation is modulated by the state of keratinocyte proliferation and differentiation and is influenced by calcium and undefined factors in serum. The data are consistent with the possibility that IFNγ alters keratinocyte differentiation in part by regulating 1,25-(OH)2D production. (Endocrinology124: 655–660, 1989)
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