Campbell V W, Del Valle J, Hawn M, Park J, Yamada T
Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor 48109-0682.
Am J Physiol. 1989 Mar;256(3 Pt 1):G631-6. doi: 10.1152/ajpgi.1989.256.3.G631.
The participation of carbonic anhydrase (CA II) in the gastric acid secretory process has been the subject of considerable controversy. We utilized a cDNA probe for CA II to measure CA II gene expression in canine gastric parietal cells that had been stimulated with the three principal acid secretagogues, carbachol, gastrin, and histamine. Hybridization to dot blots of total parietal cell RNA showed a significant increase in specific CA II mRNA content within minutes of secretagogue addition: carbachol stimulation led to an increase of 52 +/- 8.9%, reaching a maximum within 20 min; gastrin stimulation led to an increase within 60 min of 104 +/- 10.6%; stimulation with histamine was followed within 20 min by an increase of 30 +/- 7.2%. We also measured transcription rates for the CA II gene in cells stimulated by each agent and found an increase within 15 min. Our results show that CA II gene expression is regulated by agents that stimulate the parietal cell to secrete acid and that the accumulation of CA II mRNA subsequent to the initial interaction of stimulant appears to result from new transcription of the CA II gene. These data suggest the participation of CA II in the acid secretory response of the parietal cell to secretagogues.
碳酸酐酶(CA II)在胃酸分泌过程中的参与一直是相当有争议的话题。我们利用CA II的cDNA探针来测量犬胃壁细胞中CA II基因的表达,这些胃壁细胞已用三种主要的胃酸分泌刺激剂——卡巴胆碱、胃泌素和组胺进行了刺激。与壁细胞总RNA斑点杂交显示,在添加刺激剂后的几分钟内,特异性CA II mRNA含量显著增加:卡巴胆碱刺激导致增加52±8.9%,在20分钟内达到最大值;胃泌素刺激在60分钟内导致增加104±10.6%;组胺刺激在20分钟内导致增加30±7.2%。我们还测量了每种试剂刺激的细胞中CA II基因的转录速率,发现在15分钟内增加。我们的结果表明,CA II基因表达受刺激壁细胞分泌酸的试剂调节,并且在刺激剂初始相互作用后CA II mRNA的积累似乎是由CA II基因的新转录引起的。这些数据表明CA II参与了壁细胞对分泌刺激剂的酸分泌反应。