G protein-coupled receptors for lysophosphatidylethanolamine

Soojin Park, D. Im
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引用次数: 2

Abstract

Lysophospholipids like lysophosphatidic acid (LPA) and sphingosine 1-phosphate have been intensively studied over the last several decades, and these studies have resulted in the identification of their G protein-coupled receptors (GPCR) and in the discoveries of new drugs targeting GPCRs. However, lysophosphatidylethanolamine (LPE) has not attracted much research attention. Recently, we found several interesting points regarding the action and signaling of LPE, that is, its cell-type dependence, structure specificity, and unique signaling. In particular, LPE signaling through LPA 1 receptor (type 1 lysophosphatidic acid receptor) was found to be cell type dependent, and LPEs with different chain lengths induced different responses in different cells without LPA 1 involvement. Here, we review recent findings and propose possible action modes of LPE GPCRs in different cells.
溶血磷脂酰乙醇胺G蛋白偶联受体
溶血磷脂如溶血磷脂酸(LPA)和鞘氨醇1-磷酸在过去的几十年里得到了广泛的研究,这些研究导致了它们的G蛋白偶联受体(GPCR)的鉴定和针对GPCR的新药的发现。然而,溶血磷脂酰乙醇胺(LPE)并没有引起太多的研究关注。最近,我们发现了LPE的作用和信号传导的几个有趣的点,即它的细胞类型依赖性、结构特异性和独特的信号传导。特别是通过LPA 1受体(1型溶血磷脂酸受体)传递的LPE信号被发现是细胞类型依赖的,不同链长的LPE在没有LPA 1参与的不同细胞中诱导不同的反应。在这里,我们回顾了最近的发现,并提出了LPE gpcr在不同细胞中的可能作用模式。
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