School of Optometry, University of Montreal , Montreal, Quebec H3T 1P1, Canada.
School of Optometry, University of Montreal, Montreal, Quebec H3T 1P1, Canada; VIB Vesalius Research Center, KU Leuven, Leuven, Belgium, 3000.
eNeuro. 2015 Nov 9;2(5). doi: 10.1523/ENEURO.0011-15.2015. eCollection 2015 Sep-Oct.
Guidance molecules regulate the navigation of retinal ganglion cell (RGC) projections toward targets in the visual thalamus. In this study, we demonstrate that the G-protein-coupled receptor 55 (GPR55) is expressed in the retina during development, and regulates growth cone (GC) morphology and axon growth. In vitro, neurons obtained from gpr55 knock-out (gpr55(-/-) ) mouse embryos have smaller GCs, less GC filopodia, and have a decreased outgrowth compared with gpr55(+/+) neurons. When gpr55(+/+) neurons were treated with GPR55 agonists, lysophosphatidylinositol (LPI) and O-1602, we observed a chemo-attractive effect and an increase in GC size and filopodia number. In contrast, cannabidiol (CBD) decreased the GC size and filopodia number inducing chemo-repulsion. In absence of the receptor (gpr55(-/-) ), no pharmacologic effects of the GPR55 ligands were observed. In vivo, compared to their wild-type (WT) littermates, gpr55(-/-) mice revealed a decreased branching in the dorsal terminal nucleus (DTN) and a lower level of eye-specific segregation of retinal projections in the superior colliculus (SC) and in the dorsal lateral geniculate nucleus (dLGN). Moreover, a single intraocular injection of LPI increased branching in the DTN, whereas treatment with CBD, an antagonist of GPR55, decreased it. These results indicate that GPR55 modulates the growth rate and the targets innervation of retinal projections and highlight, for the first time, an important role of GPR55 in axon refinement during development.
指导分子调节视网膜神经节细胞(RGC)投射向视觉丘脑目标的导航。在这项研究中,我们证明 G 蛋白偶联受体 55(GPR55)在发育过程中在视网膜中表达,并调节生长锥(GC)形态和轴突生长。在体外,从 gpr55 敲除(gpr55(-/-))鼠胚胎中获得的神经元具有较小的 GC,较少的 GC 丝状伪足,并且与 gpr55(+/+)神经元相比,其生长减少。当 gpr55(+/+)神经元用 GPR55 激动剂,溶血磷脂酰肌醇(LPI)和 O-1602 处理时,我们观察到趋化吸引作用以及 GC 大小和丝状伪足数量的增加。相反,大麻二酚(CBD)减少 GC 大小和丝状伪足数量诱导趋化排斥。在没有受体(gpr55(-/-))的情况下,观察不到 GPR55 配体的药理作用。在体内,与野生型(WT)同窝仔相比,gpr55(-/-)小鼠在背侧终核(DTN)中的分支减少,并且在外侧膝状体(SC)和背外侧膝状体核(dLGN)中的视网膜投射的眼特异性分离水平较低。此外,单次眼内注射 LPI 增加了 DTN 的分支,而 GPR55 的拮抗剂 CBD 的治疗则减少了分支。这些结果表明 GPR55 调节视网膜投射的生长速度和靶神经支配,并首次强调了 GPR55 在发育过程中轴突细化中的重要作用。