Kremshofer Julia, Siwetz Monika, Berghold Veronika M, Lang Ingrid, Huppertz Berthold, Gauster Martin
Institute of Cell Biology, Histology and Embryology, Medical University Graz, Harrachgasse 21/VII, 8010, Graz, Austria.
Histochem Cell Biol. 2015 Jul;144(1):49-58. doi: 10.1007/s00418-015-1321-7. Epub 2015 Apr 14.
Endocannabinoids and their G protein-coupled receptors have been suggested to play a key role in human pregnancy, by regulating important aspects such as implantation, decidualization, placentation and labor. G protein-coupled receptor 55 (GPR55) was previously postulated to be another cannabinoid receptor, since specific cannabinoids were shown to act independently of the classical cannabinoid receptors CB1 or CB2. Current knowledge about GPR55 expression and function in human placenta is very limited and motivated us to evaluate human placental GPR55 expression in relation to other human peripheral tissues and to analyze spatiotemporal GPR55 expression in human placenta. Gene expression analysis revealed low GPR55 levels in human placenta, when compared to spleen and lung, the organs showing highest GPR55 expression. Moreover, expression analysis showed 5.8 fold increased placental GPR55 expression at term compared to first trimester. Immunohistochemistry located GPR55 solely at the fetal endothelium of first trimester and term placentas. qPCR and immunocytochemistry consistently confirmed GPR55 expression in isolated primary placental arterial and venous endothelial cells. Incubation with L-α-lysophosphatidylinositol (LPI), the specific and functional ligand for GPR55, at a concentration of 1 µM, significantly enhanced migration of venous, but not arterial endothelial cells. LPI-enhanced migration was inhibited by the GPR55 antagonist O-1918, suggesting a role of the LPI-GPR55 axis in placental venous endothelium function.
内源性大麻素及其G蛋白偶联受体被认为在人类妊娠中发挥关键作用,通过调节诸如着床、蜕膜化、胎盘形成和分娩等重要方面。G蛋白偶联受体55(GPR55)先前被假定为另一种大麻素受体,因为特定的大麻素已被证明可独立于经典大麻素受体CB1或CB2发挥作用。目前关于GPR55在人胎盘中的表达和功能的知识非常有限,这促使我们评估人胎盘GPR55相对于其他人体外周组织的表达,并分析其在人胎盘中的时空表达。基因表达分析显示,与脾脏和肺相比,人胎盘中GPR55水平较低,而脾脏和肺是GPR55表达最高的器官。此外,表达分析显示,与孕早期相比,足月时胎盘GPR55表达增加了5.8倍。免疫组织化学显示,GPR55仅位于孕早期和足月胎盘的胎儿内皮细胞。qPCR和免疫细胞化学一致证实了GPR55在分离的原代胎盘动脉和静脉内皮细胞中的表达。用GPR55的特异性功能性配体L-α-溶血磷脂酰肌醇(LPI)以1µM的浓度孵育,可显著增强静脉内皮细胞而非动脉内皮细胞的迁移。LPI增强的迁移被GPR55拮抗剂O-1918抑制,表明LPI-GPR55轴在胎盘静脉内皮功能中起作用。