Bradshaw Heather B, Lee Sung Ha, McHugh Douglas
The Department of Psychological and Brain Sciences, Indiana University, Bloomington, IN 47405, USA.
Prostaglandins Other Lipid Mediat. 2009 Sep;89(3-4):131-4. doi: 10.1016/j.prostaglandins.2009.04.006. Epub 2009 Apr 18.
A large and growing family of over 70 endogenous lipids of the basic structure N-acyl amide has been identified during the last 10 years. Only a few of these lipids have been characterized for biological activity, however, those that have shown a wide-range of activity may act at G-protein coupled receptors (GPCRs). Like orphan GPCRs that are identified as being in the genome and expressed in tissue, the majority of these endogenous lipids many produced throughout the body, some predominately in nervous tissue, remain orphaned. Here, we give a brief history of these orphan lipids and highlight the activity of N-arachidonoyl glycine, and farnesyl pyrophosphate at the orphan receptors GPR18 and GPR92, respectively, as well as summarizing the biological and pharmacological data for the recently identified N-palmitoyl glycine that suggests activity at a novel GPCR. Working to deorphanize both lipids and GPCRs together provides a unique opportunity for a greater understanding of cellular signaling and a challenge to find them all a home.
在过去十年中,已鉴定出一个庞大且不断增长的家族,其中有70多种具有N-酰基酰胺基本结构的内源性脂质。然而,这些脂质中只有少数几种的生物活性得到了表征,那些显示出广泛活性的脂质可能作用于G蛋白偶联受体(GPCR)。就像在基因组中被鉴定并在组织中表达的孤儿GPCR一样,这些内源性脂质中的大多数在全身产生,有些主要在神经组织中产生,但仍然没有对应的受体。在这里,我们简要介绍这些孤儿脂质的历史,并分别强调N-花生四烯酰甘氨酸和法呢基焦磷酸在孤儿受体GPR18和GPR92上的活性,同时总结最近鉴定出的N-棕榈酰甘氨酸的生物学和药理学数据,这些数据表明其在一种新型GPCR上具有活性。共同努力使脂质和GPCR都找到对应的受体,为更深入理解细胞信号传导提供了独特的机会,同时也带来了一项挑战,即要为它们全部找到归属。