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Citric acid cycle intermediates as ligands for orphan G-protein-coupled receptors

机译:柠檬酸循环中间体作为孤儿G蛋白偶联受体的配体

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摘要

The citric acid cycle is central to the regulation of energy homeostasis and cell metabolism(1). Mutations in enzymes that catalyse steps in the citric acid cycle result in human diseases with various clinical presentations(2). The intermediates of the citric acid cycle are present at micromolar concentration in blood and are regulated by respiration, metabolism and renal reabsorption/ extrusion. Here we show that GPR91 (ref. 3), a previously orphan G-protein-coupled receptor (GPCR), functions as a receptor for the citric acid cycle intermediate succinate. We also report that GPR99 (ref. 4), a close relative of GPR91, responds to alpha-ketoglutarate, another intermediate in the citric acid cycle. Thus by acting as ligands for GPCRs, succinate and alpha-ketoglutarate are found to have unexpected signalling functions beyond their traditional roles. Furthermore, we show that succinate increases blood pressure in animals. The succinate-induced hypertensive effect involves the renin - angiotensin system and is abolished in GPR91-deficient mice. Our results indicate a possible role for GPR91 in renovascular hypertension, a disease closely linked to atherosclerosis, diabetes and renal failure(5,6).
机译:柠檬酸循环对于能量稳态和细胞代谢的调节至关重要(1)。催化柠檬酸循环过程中酶的突变会导致多种临床表现的人类疾病(2)。柠檬酸循环的中间体以血液中的微摩尔浓度存在,并受呼吸,代谢和肾脏重吸收/挤出的调节。在这里,我们显示GPR91(参考文献3),以前是孤立的G蛋白偶联受体(GPCR),起柠檬酸周期琥珀酸酯柠檬酸受体的作用。我们还报告说,GPR91的近亲GPR99(参考文献4)对柠檬酸循环中的另一种中间体α-酮戊二酸有反应。因此,通过充当GPCR的配体,发现琥珀酸酯和α-酮戊二酸酯具有超出其传统作用的出乎意料的信号传导功能。此外,我们表明琥珀酸酯会增加动物的血压。琥珀酸诱导的高血压作用涉及肾素-血管紧张素系统,在缺乏GPR91的小鼠中被取消。我们的结果表明GPR91在肾血管性高血压中可能发挥作用,该疾病与动脉粥样硬化,糖尿病和肾衰竭密切相关(5,6)。

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