Graduate Institute of Neural Regenerative Medicine, College of Medical Science and Technology, Taipei Medical University, Taipei, 11031, Taiwan; Research Center of Neuroscience, Taipei Medical University, Taipei, 11031, Taiwan; TMU Research Center of Cancer Translational Medicine, Taipei Medical University, Taipei, 11031, Taiwan.
Graduate Institute of Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei, 11031, Taiwan.
Neurosci Res. 2022 Mar;176:31-39. doi: 10.1016/j.neures.2021.10.006. Epub 2021 Oct 20.
During the neural circuit formation, neuronal growth cones must be guided precisely to their neuronal or muscle targets, which can be achieved by the activation of membrane-bound guidance receptors at the periphery. However, the mechanisms that regulate the temporal availability of these receptors remain largely unknown. TAR DNA binding protein-43 (TDP-43) has been proposed to bind with the mRNAs of guidance receptors, thus prompting us to investigate its role in axon guidance of the spinal lateral motor column (LMC) neurons into the limb mesenchyme. We first identified the TDP-43 expression in the LMC neurons at the stage of axons growth into the limb using in situ mRNA hybridization. The loss and gain of TDP-43 function in chick LMC neurons redirected their axon trajectory with opposite effects. In mice, a spinal motor neuron-specific TDP-43 deletion led to the misrouting of LMC axons. Further, ectopic TDP-43 expression increased EphB protein levels in LMC neurons, suggesting that TDP-43 mediates LMC pathfinding by regulating EphB expression. Finally, TDP-43 levels influenced the growth preference of LMC neurites against ephrin-B, but not Netrin-1 and Semaphorin ligands. Our results demonstrate that TDP-43 is essential for the ephrinB:EphB signaling-mediated axon trajectory selection of LMC subtypes into the limb.
在神经回路形成过程中,神经元生长锥必须精确地导向其神经元或肌肉靶标,这可以通过在周围激活膜结合的导向受体来实现。然而,调节这些受体的时间可用性的机制在很大程度上仍然未知。TAR DNA 结合蛋白-43(TDP-43)被提议与导向受体的 mRNA 结合,因此促使我们研究其在脊髓侧运动柱(LMC)神经元进入肢体间质的轴突导向中的作用。我们首先使用原位 mRNA 杂交在 LMC 神经元进入肢体的轴突生长阶段鉴定了 TDP-43 的表达。 chick LMC 神经元中 TDP-43 功能的缺失和获得以相反的效果改变了它们的轴突轨迹。在小鼠中,脊髓运动神经元特异性 TDP-43 缺失导致 LMC 轴突的错误布线。此外,EphB 蛋白水平在 LMC 神经元中增加,表明 TDP-43 通过调节 EphB 表达来介导 LMC 寻径。最后,TDP-43 水平影响 LMC 突起对 Ephrin-B 的生长偏好,但不影响 Netrin-1 和 Semaphorin 配体。我们的结果表明,TDP-43 是 LMC 亚型进入肢体的 EphrinB:EphB 信号介导的轴突轨迹选择所必需的。