Berg J P, Ree A H, Sandvik J A, Taskén K, Landmark B F, Torjesen P A, Haug E
Hormone Laboratory, Aker Hospital, Oslo, Norway.
J Biol Chem. 1994 Dec 23;269(51):32233-8.
1,25-Dihydroxyvitamin D3 (1,25(OH)2D3) attenuates the stimulatory effects of cAMP on proliferation and iodide uptake in rat thyroid FRTL-5 cells. This study examines the effects of 1,25-(OH)2D3 on the cAMP-dependent protein kinase (PKA). Cytosol proteins separated by anion exchange chromatography showed increased [3H]cAMP binding activity as well as increased kinase activity in the fractions containing PKA type II in 1,25-(OH)2D3 (10 nM)-treated cells compared to the control cells. Western blot analysis of 1,25-(OH)2D3-treated cells revealed a 4-fold increase in the cytosolic amount of the PKA regulatory subunit RII beta, whereas no changes were detected in the regulatory subunits RI alpha and RII alpha or the catalytic (C) subunit. Northern blot analyses showed a similar increase in RII beta mRNA in cells treated for 12 h with 1,25-(OH)2D3 (10 nM), and RII beta mRNA increased further to 10-fold above control cell level after 96 h of incubation. Iodide uptake was synergistically stimulated with both PKAI- and PKAII-directed pairs of cAMP analogs. The PKAI synergism was, however, inhibited by 1,25-(OH)2D3 treatment of the cells, whereas the PKAII synergism was unaffected. In conclusion, 1,25-(OH)2D3 attenuates both PKAI formation and PKAI-stimulated iodide uptake in rat thyroid FRTL-5 cells by increasing the level of RII beta without altering the other PKA subunit levels.
1,25 - 二羟基维生素D3(1,25(OH)2D3)可减弱环磷酸腺苷(cAMP)对大鼠甲状腺FRTL - 5细胞增殖和碘摄取的刺激作用。本研究检测了1,25 - (OH)2D3对cAMP依赖性蛋白激酶(PKA)的影响。与对照细胞相比,经1,25 - (OH)2D3(10 nM)处理的细胞中,通过阴离子交换色谱分离的胞质蛋白在含有II型PKA的组分中显示出[3H]cAMP结合活性增加以及激酶活性增加。对经1,25 - (OH)2D3处理的细胞进行蛋白质印迹分析显示,PKA调节亚基RIIβ的胞质含量增加了4倍,而调节亚基RIα和RIIα或催化(C)亚基未检测到变化。Northern印迹分析显示,用1,25 - (OH)2D3(10 nM)处理12小时的细胞中RIIβ mRNA有类似增加,孵育96小时后,RIIβ mRNA进一步增加至对照细胞水平的10倍以上。碘摄取受到PKAI和PKAII导向的cAMP类似物对的协同刺激。然而,细胞经1,25 - (OH)2D3处理后,PKAI协同作用受到抑制,而PKAII协同作用未受影响。总之,1,25 - (OH)2D3通过增加RIIβ水平而不改变其他PKA亚基水平,减弱大鼠甲状腺FRTL - 5细胞中PKAI的形成和PKAI刺激的碘摄取。