Xing Lei, Larsen Rylan S, Bjorklund George Reed, Li Xiaoyan, Wu Yaohong, Philpot Benjamin D, Snider William D, Newbern Jason M
University of North Carolina Neuroscience Center, The University of North Carolina School of Medicine, Chapel Hill, United States.
Allen Institute for Brain Science, Seattle, United States.
Elife. 2016 Feb 5;5:e11123. doi: 10.7554/eLife.11123.
Aberrant signaling through the Raf/MEK/ERK (ERK/MAPK) pathway causes pathology in a family of neurodevelopmental disorders known as 'RASopathies' and is implicated in autism pathogenesis. Here, we have determined the functions of ERK/MAPK signaling in developing neocortical excitatory neurons. Our data reveal a critical requirement for ERK/MAPK signaling in the morphological development and survival of large Ctip2(+) neurons in layer 5. Loss of Map2k1/2 (Mek1/2) led to deficits in corticospinal tract formation and subsequent corticospinal neuron apoptosis. ERK/MAPK hyperactivation also led to reduced corticospinal axon elongation, but was associated with enhanced arborization. ERK/MAPK signaling was dispensable for axonal outgrowth of layer 2/3 callosal neurons. However, Map2k1/2 deletion led to reduced expression of Arc and enhanced intrinsic excitability in both layers 2/3 and 5, in addition to imbalanced synaptic excitation and inhibition. These data demonstrate selective requirements for ERK/MAPK signaling in layer 5 circuit development and general effects on cortical pyramidal neuron excitability.
通过Raf/MEK/ERK(ERK/MAPK)信号通路的异常信号传导会导致一类被称为“RAS病”的神经发育障碍的病理变化,并与自闭症发病机制有关。在这里,我们确定了ERK/MAPK信号在发育中的新皮质兴奋性神经元中的功能。我们的数据揭示了ERK/MAPK信号在第5层大型Ctip2(+)神经元的形态发育和存活中的关键需求。Map2k1/2(Mek1/2)的缺失导致皮质脊髓束形成缺陷以及随后的皮质脊髓神经元凋亡。ERK/MAPK的过度激活也导致皮质脊髓轴突伸长减少,但与分支增加有关。ERK/MAPK信号对于第2/3层胼胝体神经元的轴突生长是可有可无的。然而,Map2k1/2的缺失除了导致突触兴奋和抑制失衡外,还导致第2/3层和第5层中Arc表达减少以及内在兴奋性增强。这些数据证明了ERK/MAPK信号在第5层回路发育中的选择性需求以及对皮质锥体神经元兴奋性的总体影响。