Bikle D D, Pillai S, Gee E, Hincenbergs M
Endocrine Research Section, University of California, San Francisco.
Endocrinology. 1991 Jul;129(1):33-8. doi: 10.1210/endo-129-1-33.
The keratinocyte has receptors for, responds to, and produces both tumor necrosis factor-alpha (TNF) and 1,25-dihydroxyvitamin D [1,25-(OH)2D]. Both TNF and 1,25-(OH)2D facilitate the differentiation of keratinocytes. To explore the possibility that TNF stimulates keratinocyte differentiation at least in part by regulating 1,25-(OH)2D production we examined the effect of TNF on both 1,25-(OH)2D production and differentiation (transglutaminase activity, cornified envelope formation) at different stages of differentiation. 1,25-(OH)2D production, transglutaminase activity, and cornified envelope formation are sequentially increased during differentiation such that 1,25-(OH)2D production occurs first, followed by transglutaminase activity and, finally, cornified envelope formation. In preconfluent cells, TNF stimulated 1,25-(OH)2D production. Interferon-gamma also stimulated 1,25-(OH)2D production at low concentrations, but this was not additive to that by TNF. The stimulatory effect of TNF was maximal after 1-2 days of incubation and decreased with prolonged incubation. TNF had little effect on cornified envelope formation and transglutaminase activity in the preconfluent cells. Once keratinocytes achieved confluence, TNF stimulated transglutaminase activity and cornified envelope formation, but inhibited 1,25-(OH)2D production. Our results suggest that TNF regulates 1,25-(OH)2D production as part of its ability to accelerate keratinocyte differentiation; whether TNF stimulates or inhibits 1,25-(OH)2D production depends on whether TNF is added before or after the cell has reached its maximal capacity to make 1,25-(OH)2D.
角质形成细胞拥有肿瘤坏死因子-α(TNF)和1,25-二羟基维生素D[1,25-(OH)₂D]的受体,对其作出反应并产生这两种物质。TNF和1,25-(OH)₂D均促进角质形成细胞的分化。为了探究TNF至少部分通过调节1,25-(OH)₂D的产生来刺激角质形成细胞分化的可能性,我们在不同分化阶段研究了TNF对1,25-(OH)₂D产生及分化(转谷氨酰胺酶活性、角质包膜形成)的影响。在分化过程中,1,25-(OH)₂D的产生、转谷氨酰胺酶活性和角质包膜形成依次增加,使得1,25-(OH)₂D的产生最先发生,其次是转谷氨酰胺酶活性,最后是角质包膜形成。在未汇合的细胞中,TNF刺激1,25-(OH)₂D的产生。γ干扰素在低浓度时也刺激1,25-(OH)₂D的产生,但这与TNF的刺激作用并非相加效应。TNF的刺激作用在孵育1 - 2天后达到最大,且随着孵育时间延长而减弱。TNF对未汇合细胞中的角质包膜形成和转谷氨酰胺酶活性影响很小。一旦角质形成细胞达到汇合状态,TNF刺激转谷氨酰胺酶活性和角质包膜形成,但抑制1,25-(OH)₂D的产生。我们的结果表明,TNF调节1,25-(OH)₂D的产生是其加速角质形成细胞分化能力的一部分;TNF刺激还是抑制1,25-(OH)₂D的产生取决于TNF是在细胞达到产生1,25-(OH)₂D的最大能力之前还是之后添加。