Kotani M, Detheux M, Vandenbogaerde A, Communi D, Vanderwinden J M, Le Poul E, Brézillon S, Tyldesley R, Suarez-Huerta N, Vandeput F, Blanpain C, Schiffmann S N, Vassart G, Parmentier M
Institut de Recherche Interdisciplinare en Biologie Humaine et Nucléaire (I.R.I.B.H.N.), Brussels, Belgium.
J Biol Chem. 2001 Sep 14;276(37):34631-6. doi: 10.1074/jbc.M104847200. Epub 2001 Jul 16.
Natural peptides displaying agonist activity on the orphan G protein-coupled receptor GPR54 were isolated from human placenta. These 54-, 14,- and 13-amino acid peptides, with a common RF-amide C terminus, derive from the product of KiSS-1, a metastasis suppressor gene for melanoma cells, and were therefore designated kisspeptins. They bound with low nanomolar affinities to rat and human GPR54 expressed in Chinese hamster ovary K1 cells and stimulated PIP(2) hydrolysis, Ca(2+) mobilization, arachidonic acid release, ERK1/2 and p38 MAP kinase phosphorylation, and stress fiber formation but inhibited cell proliferation. Human GPR54 was highly expressed in placenta, pituitary, pancreas, and spinal cord, suggesting a role in the regulation of endocrine function. Stimulation of oxytocin secretion after kisspeptin administration to rats confirmed this hypothesis.
从人胎盘中分离出了对孤儿G蛋白偶联受体GPR54具有激动剂活性的天然肽。这些由54个、14个和13个氨基酸组成的肽,其C末端具有共同的RF-酰胺结构,来源于黑色素瘤细胞转移抑制基因KiSS-1的产物,因此被命名为亲吻素。它们以低纳摩尔亲和力与中国仓鼠卵巢K1细胞中表达的大鼠和人GPR54结合,并刺激磷脂酰肌醇-4,5-二磷酸(PIP₂)水解、钙离子动员、花生四烯酸释放、细胞外信号调节激酶1/2(ERK1/2)和p38丝裂原活化蛋白激酶(MAP激酶)磷酸化以及应力纤维形成,但抑制细胞增殖。人GPR54在胎盘、垂体、胰腺和脊髓中高度表达,提示其在内分泌功能调节中发挥作用。向大鼠注射亲吻素后刺激催产素分泌证实了这一假说。