Department of Pharmacology, Max-Planck-Institute for Heart and Lung Research, Ludwigstr. 43, 61231 Bad Nauheim, Germany.
Trends Pharmacol Sci. 2009 Nov;30(11):557-62. doi: 10.1016/j.tips.2009.09.001.
G-protein-coupled receptors (GPCRs) are the most versatile receptor family as they have the ability to respond to chemically diverse ligands. Despite intensive efforts during the past two decades, there are still more than 100 orphan GPCRs for which endogenous ligands are unknown. Recently, GPR109A, GPR109B and GPR81, which form a GPCR subfamily, have been deorphanized. The physiological ligands of these receptors are the ketone body 3-hydroxy-butyrate, the metabolite 2-hydroxy-propanoate (lactate) as well as the beta-oxidation intermediate 3-hydroxy-octanoate. Thus, this receptor subfamily is activated by hydroxy-carboxylic acid ligands which are intermediates of energy metabolism. All three receptors are predominantly expressed in adipocytes and mediate antilipolytic effects. In this article, we propose that the hydroxy-carboxylic acid structure of their endogenous ligands is the defining property of this receptor subfamily and that hydroxy-carboxylic acid receptors function as metabolic sensors which fine-tune the regulation of metabolic pathways.
G 蛋白偶联受体(GPCRs)是最具多功能性的受体家族,因为它们能够对化学性质多样的配体做出反应。尽管在过去的二十年里进行了密集的研究,但仍有 100 多种孤儿 GPCR 其内源性配体尚不清楚。最近,GPR109A、GPR109B 和 GPR81 这三种受体形成了一个 GPCR 亚家族,现已被发现。这些受体的生理配体是酮体 3-羟基丁酸、代谢物 2-羟基丙酸(乳酸)以及β-氧化中间产物 3-羟基辛酸。因此,这个受体亚家族被羟羧酸配体激活,而羟羧酸配体是能量代谢的中间产物。这三种受体主要在脂肪细胞中表达,介导抗脂肪分解作用。在本文中,我们提出其内源性配体的羟基羧酸结构是该受体亚家族的决定性特征,并且羟基羧酸受体作为代谢传感器,精细调节代谢途径的调节。