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Am J Physiol Gastrointest Liver Physiol ; 309(2): G78-86, 2015 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-25977510

RESUMO

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.


Assuntos
Movimento Celular , Células Epiteliais/enzimologia , Mucosa Gástrica/enzimologia , Gastrinas/metabolismo , Metaloproteinase 1 da Matriz/metabolismo , Animais , Estudos de Casos e Controles , Movimento Celular/efeitos dos fármacos , Células Cultivadas , Células Epiteliais/efeitos dos fármacos , Mucosa Gástrica/efeitos dos fármacos , Gastrinas/sangue , Gastrinas/genética , Humanos , Metaloproteinase 1 da Matriz/genética , Camundongos , Proteína Quinase 1 Ativada por Mitógeno/metabolismo , Proteína Quinase 3 Ativada por Mitógeno/metabolismo , Proteína Quinase C/metabolismo , Inibidores da Bomba de Prótons/farmacologia , RNA Mensageiro/metabolismo , Ratos , Transdução de Sinais , Transfecção , Regulação para Cima
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