Kumar J Dinesh, Steele Islay, Moore Andrew R, Murugesan Senthil V, Rakonczay Zoltan, Venglovecz Viktoria, Pritchard D Mark, Dimaline Rodney, Tiszlavicz Laszlo, Varro Andrea, Dockray Graham J
Department of Cellular and Molecular Physiology, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom; and.
Department of Pathology, University of Szeged, Szeged, Hungary.
Am J Physiol Gastrointest Liver Physiol. 2015 Jul 15;309(2):G78-86. doi: 10.1152/ajpgi.00084.2015. Epub 2015 May 14.
The pyloric antral hormone gastrin plays a role in remodeling of the gastric epithelium, but the specific targets of gastrin that mediate these effects are poorly understood. Glandular epithelial cells of the gastric corpus express matrix metalloproteinase (MMP)-1, which is a potential determinant of tissue remodeling; some of these cells express the CCK-2 receptor at which gastrin acts. We have now examined the hypothesis that gastrin stimulates expression of MMP-1 in the stomach. We determined MMP-1 transcript abundance in gastric mucosal biopsies from Helicobacter pylori negative human subjects with normal gastric mucosal histology, who had a range of serum gastrin concentrations due in part to treatment with proton pump inhibitors (PPI). The effects of gastrin were studied on gastric epithelial AGS-GR cells using Western blot and migration assays. In human subjects with increased serum gastrin due to PPI usage, MMP-1 transcript abundance was increased 2-fold; there was also increased MMP-7 transcript abundance but not MMP-3. In Western blots, gastrin increased proMMP-1 abundance, as well that of a minor band corresponding to active MMP-1, in the media of AGS-GR cells, and the response was mediated by protein kinase C and p42/44 MAP kinase. There was also increased MMP-1 enzyme activity. Gastrin-stimulated AGS-GR cell migration in both scratch wound and Boyden chamber assays was inhibited by MMP-1 immunoneutralization. We conclude that MMP-1 expression is a target of gastrin implicated in mucosal remodeling.
幽门窦激素胃泌素在胃上皮重塑中发挥作用,但介导这些效应的胃泌素具体靶点尚不清楚。胃体部的腺上皮细胞表达基质金属蛋白酶(MMP)-1,它是组织重塑的一个潜在决定因素;其中一些细胞表达胃泌素作用的CCK-2受体。我们现在检验了胃泌素刺激胃中MMP-1表达的假说。我们测定了幽门螺杆菌阴性、胃黏膜组织学正常的人类受试者胃黏膜活检组织中MMP-1转录本丰度,这些受试者血清胃泌素浓度各异,部分原因是使用了质子泵抑制剂(PPI)。利用蛋白质印迹法和迁移试验研究了胃泌素对胃上皮AGS-GR细胞的影响。在因使用PPI导致血清胃泌素升高的人类受试者中,MMP-1转录本丰度增加了2倍;MMP-7转录本丰度也增加了,但MMP-3没有增加。在蛋白质印迹中,胃泌素增加了AGS-GR细胞培养基中前MMP-1的丰度以及与活性MMP-1对应的一条小带的丰度,且该反应由蛋白激酶C和p42/44丝裂原活化蛋白激酶介导。MMP-1酶活性也增加了。在划痕试验和博伊登小室试验中,MMP-1免疫中和抑制了胃泌素刺激的AGS-GR细胞迁移。我们得出结论,MMP-1表达是胃泌素参与黏膜重塑的一个靶点。