School of Life Sciences, Arizona State University, Tempe, AZ 85287, USA.
School of Biological and Health Systems Engineering, Arizona State University, Tempe, AZ 85287, USA.
Dis Model Mech. 2024 Jun 1;17(6). doi: 10.1242/dmm.050570. Epub 2024 Jul 2.
Abnormal extracellular signal-regulated kinase 1/2 (ERK1/2, encoded by Mapk3 and Mapk1, respectively) signaling is linked to multiple neurodevelopmental diseases, especially the RASopathies, which typically exhibit ERK1/2 hyperactivation in neurons and non-neuronal cells. To better understand how excitatory neuron-autonomous ERK1/2 activity regulates forebrain development, we conditionally expressed a hyperactive MEK1 (MAP2K1) mutant, MEK1S217/221E, in cortical excitatory neurons of mice. MEK1S217/221E expression led to persistent hyperactivation of ERK1/2 in cortical axons, but not in soma/nuclei. We noted reduced axonal arborization in multiple target domains in mutant mice and reduced the levels of the activity-dependent protein ARC. These changes did not lead to deficits in voluntary locomotion or accelerating rotarod performance. However, skilled motor learning in a single-pellet retrieval task was significantly diminished in these MEK1S217/221E mutants. Restriction of MEK1S217/221E expression to layer V cortical neurons recapitulated axonal outgrowth deficits but did not affect motor learning. These results suggest that cortical excitatory neuron-autonomous hyperactivation of MEK1 is sufficient to drive deficits in axon outgrowth, which coincide with reduced ARC expression, and deficits in skilled motor learning. Our data indicate that neuron-autonomous decreases in long-range axonal outgrowth may be a key aspect of neuropathogenesis in RASopathies.
异常细胞外信号调节激酶 1/2(ERK1/2,分别由 Mapk3 和 Mapk1 编码)信号与多种神经发育疾病有关,特别是 RAS 相关疾病,其神经元和非神经元细胞中通常表现出 ERK1/2 的过度激活。为了更好地理解兴奋性神经元自主 ERK1/2 活性如何调节前脑发育,我们在小鼠皮质兴奋性神经元中条件性表达了一种过度活跃的 MEK1(MAP2K1)突变体 MEK1S217/221E。MEK1S217/221E 的表达导致皮质轴突中 ERK1/2 的持续过度激活,但在体/核中没有。我们注意到突变小鼠多个靶域的轴突分支减少,活性依赖性蛋白 ARC 的水平降低。这些变化并没有导致自愿运动或加速旋转棒性能的缺陷。然而,在单次取食任务中的熟练运动学习在这些 MEK1S217/221E 突变体中显著减少。将 MEK1S217/221E 的表达限制在皮质 V 层神经元中重现了轴突生长缺陷,但没有影响运动学习。这些结果表明,皮质兴奋性神经元自主的 MEK1 过度激活足以导致轴突生长缺陷,这与 ARC 表达减少以及熟练运动学习缺陷相吻合。我们的数据表明,长程轴突生长的神经元自主减少可能是 RAS 相关疾病神经发病机制的一个关键方面。