Hla Timothy
Center for Vascular Biology, Department of Cell Biology, University of Connecticut Health Center, Farmington, CT 06030, USA.
Prostaglandins Other Lipid Mediat. 2005 Sep;77(1-4):197-209. doi: 10.1016/j.prostaglandins.2005.06.008.
G protein-coupled receptors (GPCR) are used ubiquitously and widely for signal transduction across the plasma membrane. The ligands for GPCRs are structurally diverse and include peptides, odorants, photon, ions and lipids. It is thought that GPCRs evolved by gene duplication and mutational events that diversified the ligand binding and signaling properties, thereby resulting in paralogues in various organisms. Genomic sequencing efforts of various organisms indicate that GPCRs evolved very early in evolution; for example, unicellular eukaryotes use GPCRs for mating, differentiation and sporulation responses and prokarotes utilize these receptors for phototransduction, as exemplified by the bacteriorhodopsin, a photon sensor. Many GPCRs fall into subfamilies, usually determined by structural similarity to their ligands. Bioactive lipids such as lysophospholipids, eicosanoids, ether lipids and endocannabinoids, which are produced widely in evolution, also signal through GPCRs. Thus, distinct subfamilies of bioactive lipid GPCRs, such as prostanoid receptors, lysophosphatidic, sphingosine 1-phosphate, leukotrienes, hydroxy fatty acids, endocannabinoids and ether lipids exist in the mammalian genome. With the increasing availability of genomic information throughout the phylogenetic tree, orthologues of bioactive lipid receptors are found in the genomes of vertebrates and chordates but not in worms, flies or other lower organisms. This is in contrast to GPCRs for biogenic amines and polypeptide growth factors, which are conserved in invertebrates as well. Thus, it appears that with the evolution of chordates, lipids may have acquired novel roles in cell-cell communication events via GPCRs. This hypothesis will be discussed using the prostanoid and lysophospholipid signaling systems. Since such bioactive lipids play critical roles in immune, vascular and nervous systems, this suggests that lipid metabolite signaling via the GPCRs co-evolved with the development of sophisticated vascular, immune and nervous systems in chordates and vertebrates.
G蛋白偶联受体(GPCR)广泛且普遍地用于跨质膜的信号转导。GPCR的配体在结构上多种多样,包括肽、气味分子、光子、离子和脂质。据认为,GPCR是通过基因复制和突变事件进化而来的,这些事件使配体结合和信号特性多样化,从而在各种生物体中产生了旁系同源物。对各种生物体的基因组测序结果表明,GPCR在进化过程中很早就出现了;例如,单细胞真核生物利用GPCR进行交配、分化和孢子形成反应,原核生物利用这些受体进行光转导,细菌视紫红质(一种光子传感器)就是例证。许多GPCR属于亚家族,通常由与其配体的结构相似性来确定。生物活性脂质,如溶血磷脂、类二十烷酸、醚脂和内源性大麻素,在进化过程中广泛产生,它们也通过GPCR进行信号传导。因此,在哺乳动物基因组中存在生物活性脂质GPCR的不同亚家族,如前列腺素受体、溶血磷脂酸、1-磷酸鞘氨醇、白三烯、羟基脂肪酸、内源性大麻素和醚脂。随着整个系统发育树中基因组信息的可用性不断增加,在脊椎动物和脊索动物的基因组中发现了生物活性脂质受体的直系同源物,但在蠕虫、苍蝇或其他低等生物中未发现。这与生物胺和多肽生长因子的GPCR形成对比,后者在无脊椎动物中也保守存在。因此,随着脊索动物的进化,脂质似乎可能通过GPCR在细胞间通讯事件中获得了新的作用。将使用前列腺素和溶血磷脂信号系统来讨论这一假设。由于此类生物活性脂质在免疫、血管和神经系统中起关键作用,这表明通过GPCR的脂质代谢物信号传导与脊索动物和脊椎动物中复杂的血管、免疫和神经系统的发育共同进化。