Soff G A, Cornwell T L, Cundiff D L, Gately S, Lincoln T M
Department of Medicine, Northwestern University Medical School, Chicago, Illinois 60611, USA.
J Clin Invest. 1997 Nov 15;100(10):2580-7. doi: 10.1172/JCI119801.
A key component of the nitric oxide-cyclic guanosine monophosphate (cGMP) pathway in smooth muscle cells (SMC) is the type I GMP-dependent protein kinase (PK-G I). Activation of PK-G I mediates the reduction of cytoplasmic calcium concentrations and vasorelaxation. In this manuscript, we demonstrate that continuous exposure of SMC in culture to the nitrovasodilators S-nitroso-N-acetylpenicillamine (SNAP) or sodium nitroprusside (SNP) results in approximately 75% suppression of PK-G I mRNA by 48 h. PK-G I mRNA and protein were also suppressed by continuous exposure to cGMP analogues 8-bromo- and 8-(4-chlorophenylthio) guanosine-3,5-monophosphate or the cAMP analogue dibutyryl cAMP. These results suggest that activation of one or both of the cyclic nucleotide-dependent protein kinases mediates PK-G I mRNA suppression. Using isoform-specific cDNA probes, only the PK-G I alpha was detected in SMC, either at baseline or after suppression, while PK-G I beta was not detected, indicating that isoform switch was not contributing to the gene regulation. Using the transcription inhibitor actinomycin D, the PK-G I mRNA half-life in bovine SMC was observed to be 5 h. The half-life was not affected by the addition of SNAP to actinomycin D, indicating no effect on PK-G I mRNA stability. Nuclear runoff studies indicated a suppression of PK-G I gene transcription by SNAP. PK-G I suppression was also observed in vivo in rats given isosorbide dinitrate in the drinking water, with a dose-dependent suppression of PK-G I protein in the aorta. PK-G I antigen in whole rat lung extract was also suppressed by administration of isosorbide or theophylline in the drinking water. These data may contribute to our understanding of nitrovasodilator resistance, a phenomenon resulting from continuous exposure to nitroglycerin or other nitrovasodilators.
平滑肌细胞(SMC)中一氧化氮-环磷酸鸟苷(cGMP)信号通路的一个关键成分是I型cGMP依赖性蛋白激酶(PK-G I)。PK-G I的激活介导细胞质钙浓度降低和血管舒张。在本论文中,我们证明,将培养的SMC持续暴露于硝基血管扩张剂S-亚硝基-N-乙酰青霉胺(SNAP)或硝普钠(SNP)48小时后,PK-G I mRNA会被抑制约75%。持续暴露于cGMP类似物8-溴-和8-(4-氯苯硫基)鸟苷-3,5-单磷酸或cAMP类似物二丁酰cAMP也会抑制PK-G I mRNA和蛋白。这些结果表明,一种或两种环核苷酸依赖性蛋白激酶的激活介导了PK-G I mRNA的抑制。使用亚型特异性cDNA探针,在SMC中,无论是在基线还是抑制后,仅检测到PK-G Iα,而未检测到PK-G Iβ,这表明亚型转换对基因调控没有影响。使用转录抑制剂放线菌素D,观察到牛SMC中PK-G I mRNA的半衰期为5小时。向放线菌素D中添加SNAP不会影响半衰期,表明对PK-G I mRNA稳定性没有影响。核转录分析表明,SNAP抑制了PK-G I基因转录。在给饮用水中添加异山梨醇二硝酸酯的大鼠体内也观察到了PK-G I的抑制,主动脉中PK-G I蛋白的抑制呈剂量依赖性。给饮用水中添加异山梨醇或茶碱也会抑制全大鼠肺提取物中的PK-G I抗原。这些数据可能有助于我们理解硝基血管扩张剂抵抗,这是一种因持续暴露于硝酸甘油或其他硝基血管扩张剂而产生的现象。