Bikle D D, Pillai S, Gee E, Hincenbergs M
Veterans Administration Medical Center, San Francisco, California 94121.
Endocrinology. 1989 Feb;124(2):655-60. doi: 10.1210/endo-124-2-655.
Interferon-gamma (IFN gamma) 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 IFN gamma 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 IFN gamma 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 IFN gamma. Postconfluent keratinocytes did not respond to 1.8 nM IFN gamma. The production of 1,25-(OH)2D by keratinocytes grown in serum-free medium was maximally stimulated by 0.006 nM IFN gamma and inhibited at concentrations greater than 0.06 nM. Keratinocytes grown in 0.1 mM calcium serum-free medium (which prevents differentiation) were more sensitive to both the stimulatory and inhibitory effects of IFN gamma than keratinocytes grown in 1.2 mM calcium serum-free medium (which permits differentiation). The stimulatory effect of IFN gamma 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 IFN gamma concentrations and increasingly greater inhibition at the higher IFN gamma concentrations. The inhibitory effects of IFN gamma on 1,25-(OH)2D production paralleled the inhibitory effects of IFN gamma on cell growth. Thus, IFN gamma 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 IFN gamma alters keratinocyte differentiation in part by regulating 1,25-(OH)2D production.
γ干扰素(IFNγ)和1,25 - 二羟基维生素D [1,25 - (OH)₂D] 对角质形成细胞均具有强大的抗增殖和促分化作用。由于角质形成细胞能产生1,25 - (OH)₂D,我们探讨了IFNγ部分通过调节1,25 - (OH)₂D的产生而作用于角质形成细胞的可能性。在评估其产生1,25 - (OH)₂D的能力之前,我们将人新生儿包皮角质形成细胞在不同浓度的IFNγ存在下培养不同时间。在血清(会延迟分化)存在的情况下生长的未汇合角质形成细胞产生1,25 - (OH)₂D的能力受到1.8 nM IFNγ的刺激。汇合后的角质形成细胞对1.8 nM IFNγ无反应。在无血清培养基中生长的角质形成细胞产生1,25 - (OH)₂D的能力在0.006 nM IFNγ时受到最大刺激,而在浓度大于0.06 nM时受到抑制。在0.1 mM钙的无血清培养基(可防止分化)中生长的角质形成细胞比在1.2 mM钙的无血清培养基(允许分化)中生长的角质形成细胞对IFNγ的刺激和抑制作用更敏感。IFNγ对1,25 - (OH)₂D产生的刺激作用在孵育2天后达到最大。孵育时间超过2天,在低IFNγ浓度下刺激作用逐渐减弱,在高IFNγ浓度下抑制作用逐渐增强。IFNγ对1,25 - (OH)₂D产生的抑制作用与IFNγ对细胞生长的抑制作用平行。因此,IFNγ确实调节角质形成细胞产生1,25 - (OH)₂D。然而,这种调节受到角质形成细胞增殖和分化状态的影响,并受血清中钙和未知因素的影响。这些数据与IFNγ部分通过调节1,25 - (OH)₂D的产生来改变角质形成细胞分化的可能性一致。