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Proton-sensing G-protein-coupled receptors

机译:质子敏感的G蛋白偶联受体

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Blood pH is maintained in a narrow range around pH 7.4 mainly through regulation of respiration and renal acid extrusion. The molecular mechanisms involved in pH homeostasis are not completely understood. Here we show that ovarian cancer G-protein-coupled receptor 1 (OGR1), previously described as a receptor for sphingosylphosphorylcholine, acts as a proton-sensing receptor stimulating inositol phosphate formation. The receptor is inactive at pH 7.8, and fully activated at pH 6.8―site- directed mutagenesis shows that histidines at the extracellular surface are involved in pH sensing. We find that GPR4, a close relative of OGR1, also responds to pH changes, but elicits cyclic AMP formation. It is known that the skeleton participates in pH homeostasis as a buffering organ, and that osteoblasts respond to pH changes in the physiological range, but the pH-sensing mechanism operating in these cells was hitherto not known. We detect expression of OGR1 in osteosarcoma cells and primary human osteoblast precursors, and show that these cells exhibit strong pH-dependent inositol phosphate formation. Immuno-histochemistry on rat tissue sections confirms the presence of OGR1 in osteoblasts and osteocytes. We propose that OGR1 and GPR4 are proton-sensing receptors involved in pH homeostasis.
机译:血液的pH值主要通过调节呼吸作用和肾酸排出而维持在7.4左右的窄范围内。 pH稳态涉及的分子机制尚未完全了解。在这里,我们显示卵巢癌G蛋白偶联受体1(OGR1),先前描述为鞘氨醇磷酸胆碱的受体,充当质子感应受体,刺激肌醇磷酸酯的形成。该受体在pH 7.8时无活性,在pH 6.8时被完全活化。定点诱变表明细胞外表面的组氨酸参与pH传感。我们发现,GPR4,OGR1的近亲,也响应pH值变化,但引发了环AMP的形成。已知骨架作为缓冲器官参与pH稳态,成骨细胞对生理范围内的pH变化作出反应,但是迄今为止尚不清楚在这些细胞中起作用的pH感应机制。我们检测OGR1在骨肉瘤细胞和主要的人类成骨细胞前体中的表达,并显示这些细胞表现出较强的pH依赖性肌醇磷酸形成。大鼠组织切片上的免疫组织化学证实了OGR1在成骨细胞和骨细胞中的存在。我们建议OGR1和GPR4是参与pH稳态的质子感应受体。

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