大脑皮层谷氨酸能神经元中 MEK1 的过度激活会导致投射轴突缺陷和异常运动学习。

IF 4 3区 医学 Q2 CELL BIOLOGY Disease Models & Mechanisms Pub Date : 2024-06-01 Epub Date: 2024-07-02 DOI:10.1242/dmm.050570
George R Bjorklund, Katherina P Rees, Kavya Balasubramanian, Lauren T Hewitt, Kenji Nishimura, Jason M Newbern
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引用次数: 0

摘要

细胞外调控激酶 1/2(ERK1/2)信号异常与多种神经发育疾病有关,尤其是 RAS 病,这些疾病通常表现为神经元和非神经元细胞中的 ERK1/2 过度激活。为了更好地了解兴奋性神经元自主的ERK1/2活性是如何调控前脑发育的,我们在皮质兴奋性神经元中条件表达了超活性的MEK1S217/221E。MEK1S217/221E 的表达导致了大脑皮层轴突中 ERK1/2 的持续过度激活,而在体节/核中则没有。我们注意到突变体中多个靶域的轴突分枝减少,活动依赖基因 ARC 的表达也减少。这些变化并没有导致自主运动或加速旋转能力的缺陷。然而,在这些MEK1S217/221E突变体中,单颗粒检索任务中的熟练运动学习能力明显减弱。将MEK1S217/221E的表达限制在第V层皮层神经元再现了轴突生长缺陷,但并不影响运动学习。这些结果表明,皮层兴奋性神经元自主的 MEK1 过度激活足以驱动轴突生长缺陷,而轴突生长缺陷与 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,神经元自主的长程轴突生长减少可能是RAS疾病神经发病机制的一个关键方面。
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Hyperactivation of MEK1 in cortical glutamatergic neurons results in projection axon deficits and aberrant motor learning.

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.

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来源期刊
Disease Models & Mechanisms
Disease Models & Mechanisms 医学-病理学
CiteScore
6.60
自引率
7.00%
发文量
203
审稿时长
6-12 weeks
期刊介绍: Disease Models & Mechanisms (DMM) is an online Open Access journal focusing on the use of model systems to better understand, diagnose and treat human disease.
期刊最新文献
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