Tong P, Mayes D, Wheeler L
Biochem Biophys Res Commun. 1986 Jul 16;138(1):483-8. doi: 10.1016/0006-291x(86)90306-2.
The rate of proliferation of epidermal keratinocytes was manipulated by growing the cells in medium containing high or low concentrations of calcium. Keratinocytes cultured in high extracellular Ca++ (1.4 mM and 2.8 mM) proliferated twice as fast as those grown in low Ca++ medium (0.09 mM) as measured by incorporation of [3H]thymidine into DNA. Exposure of high calcium keratinocytes to all-trans retinoic acid for 4 days caused a dose-related inhibition of DNA synthesis with an IC50 of about 10 microM. In contrast, incubating low calcium keratinocytes with all-trans retinoic acid caused a dose-related stimulation of DNA synthesis with maximum increase of 278% over control at 10 microM. This increase was accompanied by increases in culture confluency with maximum increase of 109% in cell number over control at 10 microM. These results are of importance since they suggest Ca++ may influence the effect of retinoids on keratinocytes.
通过在含有高浓度或低浓度钙的培养基中培养细胞,来控制表皮角质形成细胞的增殖速率。用[³H]胸苷掺入DNA的方法测定,在高细胞外钙离子浓度(1.4 mM和2.8 mM)条件下培养的角质形成细胞,其增殖速度是在低钙离子浓度培养基(0.09 mM)中培养的细胞的两倍。高钙条件下培养的角质形成细胞暴露于全反式维甲酸4天,会导致与剂量相关的DNA合成抑制,IC50约为10 μM。相反,在低钙条件下培养的角质形成细胞与全反式维甲酸一起孵育,会导致与剂量相关的DNA合成刺激,在10 μM时比对照最大增加278%。这种增加伴随着培养物汇合度的增加,在10 μM时细胞数量比对照最大增加109%。这些结果很重要,因为它们表明钙离子可能会影响类维生素A对角质形成细胞的作用。