首页> 外文期刊>Regulatory peptides. >Effects of ECL cell extracts and granule/vesicle-enriched fractions from rat oxyntic mucosa on cAMP and IP(3) in rat osteoblast-like cells.
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Effects of ECL cell extracts and granule/vesicle-enriched fractions from rat oxyntic mucosa on cAMP and IP(3) in rat osteoblast-like cells.

机译:ECL细胞提取物和大鼠氧化性粘膜的颗粒/囊泡富集成分对大鼠成骨样细胞cAMP和IP(3)的影响。

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摘要

The existence of an osteotropic hormone (referred to as gastrocalcin) in the ECL cells of the gastric mucosa has been suggested. Both gastrin and an extract of the oxyntic mucosa lower blood Ca(2+) and stimulate Ca(2+) uptake into bone. The ECL cells are known to operate under gastrin control and, conceivably, gastrin lowers blood Ca(2+) indirectly by releasing the hypothetical ECL cell hormone. We have shown earlier that extracts of isolated ECL cells or of the granule/vesicle fraction of the oxyntic mucosa evoke a typical Ca(2+)-mediated second messenger response in osteoblastic cells. In the present study, we characterize this response further. An increase in intracellular inositol 1,4,5-trisphosphate (IP(3)) concentration was observed after treatment of UMR-106.01 osteoblast-like cells with extracts of ECL cells or granule/vesicle-enriched fractions from oxyntic mucosa. Intracellular cyclic adenosine monophosphate (cAMP) concentrations were not affected. Inhibition of phospholipase C (PLC) by U-73122 abolished the increase in [Ca(2+)](i). Preincubation of UMR-106.01 cells with pertussis toxin, which blocks many G-proteins, did not prevent the increases in IP(3) and [Ca(2+)](i). It was also found that the novel peptide hormone ghrelin, produced in the A-like cells of the oxyntic mucosa, did not evoke any Ca(2+) signal in osteoblastic cells. The results indicate that the extracts mediate their effects through a pertussis toxin-insensitive mechanism, and that binding to a receptor leads to activation of PLC and production of IP(3) resulting in increased [Ca(2+)](i). The putative osteotropic hormone is distinct from ghrelin.
机译:已经提出在胃粘膜的ECL细胞中存在促骨质激素(称为胃钙蛋白)。胃泌素和催产性粘膜提取物均降低血液中的Ca(2+)并刺激Ca(2+)吸收到骨骼中。已知ECL细胞在胃泌素控制下运行,并且可以想象,胃泌素通过释放假定的ECL细胞激素间接降低血液Ca(2+)。我们早先已经表明,分离的ECL细胞或氧化性粘膜的颗粒/囊泡部分的提取物在成骨细胞中引起典型的Ca(2+)介导的第二信使反应。在本研究中,我们进一步表征了这种反应。用ECL细胞提取物或氧化性粘膜的颗粒/囊泡富集级分处理UMR-106.01成骨细胞样细胞后,观察到细胞内肌醇1,4,5-三磷酸(IP(3))浓度增加。细胞内环状单磷酸腺苷(cAMP)的浓度不受影响。 U-73122对磷脂酶C(PLC)的抑制作用消除了[Ca(2 +)](i)的增加。 UMR-106.01细胞与百日咳毒素的预温育可以阻止许多G蛋白,但不能阻止IP(3)和[Ca(2 +)](i)的增加。还发现在催产性粘膜的A样细胞中产生的新型肽激素ghrelin不会在成骨细胞中引起任何Ca(2+)信号。结果表明,提取物通过百日咳毒素不敏感的机制介导其作用,与受体的结合导致PLC的激活和IP(3)的产生,导致[Ca(2 +)](i)增加。推定的促骨质激素不同于生长素释放肽。

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