van Leeuwen J P, Pols H A, van den Bemd G C, Kempenaar J, Thio H B, Birkenhäger J C, Ponec M
Department of Internal Medicine III, Erasmus University Medical School, Rotterdam, The Netherlands.
Biochim Biophys Acta. 1994 Mar 31;1221(2):167-70. doi: 10.1016/0167-4889(94)90009-4.
Cultured normal human keratinocytes (NHK) provide a useful experimental model for studies of processes occurring during terminal differentiation, since the extent of keratinocyte maturation can be manipulated experimentally by modulation of extracellular calcium concentration. When NHK are maintained in low calcium (0.06 mM) medium they proliferate but do not stratify. Raising the level of calcium to 1-2 mM results within a few hours in induction of keratinocyte differentiation. Results of the present study show that formation of 1,25-(OH)2D3 is higher in NHK grown at 0.06 mM than in NHK grown at 1.6 mM calcium concentration. After 2 h exposure of low calcium cultures to 1.6 mM calcium the 1,25-(OH)2D3 production starts to decrease. On the other hand, exposure of cells cultured in 1.6 mM calcium medium to 0.06 mM calcium concentration induced already within 4 h an increase in 1,25-(OH)2D3 formation which was not accompanied by a decrease in cornified envelope formation. Thereby, the present study demonstrated that calcium can regulate 1,25-(OH)2D3 formation independently of changes in keratinocyte differentiation.
培养的正常人角质形成细胞(NHK)为研究终末分化过程中发生的现象提供了一个有用的实验模型,因为角质形成细胞的成熟程度可以通过调节细胞外钙浓度进行实验性调控。当NHK维持在低钙(0.06 mM)培养基中时,它们会增殖但不会分层。将钙水平提高到1-2 mM会在数小时内诱导角质形成细胞分化。本研究结果表明,在0.06 mM钙浓度下生长的NHK中1,25-(OH)2D3的形成高于在1.6 mM钙浓度下生长的NHK。将低钙培养物暴露于1.6 mM钙2小时后,1,25-(OH)2D3的产生开始减少。另一方面,将在1.6 mM钙培养基中培养的细胞暴露于0.06 mM钙浓度下,在4小时内就诱导了1,25-(OH)2D3形成增加,且未伴随角质包膜形成减少。因此,本研究表明钙可以独立于角质形成细胞分化的变化来调节1,25-(OH)2D3的形成。