Culvenor A J, Zabrenetzky V, Lovenberg W
Biochem Pharmacol. 1984 Aug 1;33(15):2361-6. doi: 10.1016/0006-2952(84)90706-8.
Culture of PC-12 cells in 1 microM dexamethasone for 24, 48 or 72 hr did not alter significantly PC-12 cell total biopterin levels, although tyrosine hydroxylase activity in extracts of cell homogenates was increased 2- to 3-fold. Increasing the concentration of dexamethasone to 10 microM did not change biopterin levels or result in further increases in tyrosine hydroxylase activity measured after 72 hr. Culture of cells in dexamethasone markedly decreased the ratio of biopterin concentration to tyrosine hydroxylase activity. The molar ratio of tyrosine hydroxylase subunits to biopterin in control cells can be estimated to be approximately one. Therefore, following induction of the enzyme by dexamethasone, there appears to be an excess of enzyme molecules relative to cofactor molecules in these cells.
将PC-12细胞在1微摩尔地塞米松中培养24、48或72小时,尽管细胞匀浆提取物中的酪氨酸羟化酶活性增加了2至3倍,但PC-12细胞的总生物蝶呤水平没有显著改变。将地塞米松浓度增加到10微摩尔,72小时后测量的生物蝶呤水平没有变化,酪氨酸羟化酶活性也没有进一步增加。用地塞米松培养细胞显著降低了生物蝶呤浓度与酪氨酸羟化酶活性的比值。对照细胞中酪氨酸羟化酶亚基与生物蝶呤的摩尔比估计约为1。因此,用地塞米松诱导该酶后,这些细胞中相对于辅因子分子而言,酶分子似乎过量。