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首页> 外文期刊>Life sciences >Gastrin and interleukin-1 beta stimulate growth factor secretion from cultured rabbit gastric parietal cells
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Gastrin and interleukin-1 beta stimulate growth factor secretion from cultured rabbit gastric parietal cells

机译:胃泌素和白介素-1β刺激培养的兔胃壁细胞分泌生长因子

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The hormone gastrin stimulates proliferation of the gastric mucosa. Inflammation of the stomach is also associated with increased proliferation. The proliferative response is important in the reparative response to injury but can be deleterious by predisposing to the development of cancer. Parietal cells, but not the cells in the proliferative zone of the gastric glands, express the appropriate gastrin receptor. Parietal cells may mediate the trophic effects of gastrin by secreting other growth factors. The role of parietal cells in the proliferative responses has been examined in this study. Rabbit parietal cells were cultured with gastrin or the cytokine interleukin-1beta for IS hours. The conditioned medium from gastrin or IL-1beta stimulated parietal cells increased proliferation of HeLa cells in an epidermal growth factor-receptor dependant manner. Gastrin and IL-1beta stimulated the secretion of heparin-binding epidermal growth factor and amphiregulin but not transforming growth factor-alpha from parietal cells. Combinations of gastrin and IL-1beta on growth factor secretion were synergistic. The protein kinase C inhibitor staurosporine abolished these stimulatory effects of gastrin and IL-1beta. Divergent effects on histamine-stimulated acid secretion were observed; 18 hours pre-treatment with gastrin enhanced acid secretion by 50% but IL-1beta inhibited acid secretion in both control and gastrin pre-treated parietal cells.The acid-secreting parietal cell plays a central role in the regulation of mucosal proliferation in gastric inflammation. Secretion of paracrine growth factors by parietal cells may be an important point of integration between the endocrine and inflammatory stimuli in determining mucosal responses to injury and inflammation. (C) 2004 Elsevier Inc. All rights reserved.
机译:胃泌素激素刺激胃粘膜的增殖。胃部发炎还与增殖增加有关。增殖反应在对损伤的修复反应中很重要,但由于易患癌症,因此可能有害。壁细胞表达适当的胃泌素受体,但不表达胃腺增生区中的细胞。壁细胞可通过分泌其他生长因子来介导胃泌素的营养作用。在这项研究中已经检查了壁细胞在增殖反应中的作用。兔壁细胞用胃泌素或细胞因子白介素-1β培养IS小时。来自胃泌素或IL-1β刺激的壁细胞的条件培养基以表皮生长因子受体依赖性方式增加了HeLa细胞的增殖。胃泌素和IL-1β刺激肝素结合表皮生长因子和双调蛋白的分泌,但不刺激壁细胞转化生长因子-α。胃泌素和IL-1β对生长因子分泌的组合具有协同作用。蛋白激酶C抑制剂星形孢菌素消除了胃泌素和IL-1β的这些刺激作用。观察到对组胺刺激的酸分泌有不同的影响。胃泌素预处理18小时可使酸分泌增加50%,但IL-1β抑制对照和胃泌素预处理的壁细胞中的酸分泌。分泌酸的壁细胞在胃炎症中对粘膜增殖的调节中起着核心作用。壁细胞分泌旁分泌生长因子可能是内分泌和炎性刺激之间整合的重要点,可确定粘膜对损伤和炎症的反应。 (C)2004 Elsevier Inc.保留所有权利。

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