Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL, 33136, USA.
Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, FL, 33136, USA.
Exp Eye Res. 2019 May;182:39-43. doi: 10.1016/j.exer.2019.03.004. Epub 2019 Mar 14.
Wingless-type (Wnt) signaling pathways mediate axonal growth and remodeling in the embryonic optic nerve, brain and spinal cord. Recent studies demonstrated that the canonical Wnt/β-catenin signaling pathway also induces axonal regeneration after injury in the optic nerve of adult animals. However, the molecular mechanisms of Wnt-mediated axonal growth are not well understood. Additionally, because Wnt signaling is stimulated in neurons as well as neighboring non-neuronal cells, the cell type(s) responsible for Wnt-induced axonal regeneration are not known. The objectives of this study were to investigate potential mechanisms and target cells of Wnt3a stimulated neurite growth using primary retinal ganglion cell (RGC) cultures. We demonstrated that Wnt3a ligand induced dose-dependent increases in average neurite length and number of neurites in RGCs. QPCR analysis of candidate mediators showed that Wnt3a-dependent neurite growth was associated with lower expression of Ripk1 and Ripk3 genes. Additionally, inhibiting Ripk1 signaling with Necrostatin-1s led to increased neurite number per cell but not increased neurite length. Therefore, Ripk signaling may be involved in mediating the effects of Wnt3a on neurite number but Ripk activity does not seem to be required for Wnt3a-dependent regulation of neurite length. This study shows that RGCs are direct cellular targets of Wnt3a-induced axonal growth, and we identified a novel association between Wnt signaling and Rip kinases in neurite formation.
Wnt 信号通路介导胚胎视神经、大脑和脊髓中的轴突生长和重塑。最近的研究表明,经典的 Wnt/β-连环蛋白信号通路也能诱导成年动物视神经损伤后的轴突再生。然而,Wnt 介导的轴突生长的分子机制尚不清楚。此外,由于 Wnt 信号在神经元以及邻近的非神经元细胞中都受到刺激,因此尚不清楚负责 Wnt 诱导的轴突再生的细胞类型。本研究的目的是使用原代视网膜神经节细胞(RGC)培养物来研究 Wnt3a 刺激神经突生长的潜在机制和靶细胞。我们证明了 Wnt3a 配体诱导 RGC 中平均神经突长度和神经突数量的剂量依赖性增加。候选介质的 QPCR 分析表明,Wnt3a 依赖性神经突生长与 Ripk1 和 Ripk3 基因表达降低有关。此外,用 Necrostatin-1s 抑制 Ripk1 信号会导致每个细胞的神经突数量增加,但不会增加神经突长度。因此,Ripk 信号可能参与介导 Wnt3a 对神经突数量的影响,但 Ripk 活性似乎不是 Wnt3a 依赖性调节神经突长度所必需的。本研究表明,RGC 是 Wnt3a 诱导的轴突生长的直接细胞靶标,并且我们在神经突形成中发现了 Wnt 信号与 Rip 激酶之间的新关联。