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Mef2c通过调节对 Ephrin 排斥的敏感性来控制产后胼胝体轴突靶向。

Mef2c Controls Postnatal Callosal Axon Targeting by Regulating Sensitivity to Ephrin Repulsion.

作者信息

Sudarsanam Sriram, Guzman-Clavel Luis E, Dar Nyle, Ziak Jakub, Shahid Naseer, Jin Xinyu O, Kolodkin Alex L

机构信息

Solomon H. Snyder Department of Neuroscience, The Johns Hopkins Kavli Neuroscience Discovery Institute, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.

Solomon H. Snyder Department of Neuroscience, The Johns Hopkins Kavli Neuroscience Discovery Institute, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205

出版信息

J Neurosci. 2025 May 21;45(21):e0201252025. doi: 10.1523/JNEUROSCI.0201-25.2025.

Abstract

Intracortical circuits, including long-range callosal projections, are crucial for information processing. The development of neuronal connectivity in the cerebral cortex is contingent on ordered emergence of neuronal classes followed by the formation of class-specific axon projections. However, the genetic determinants of intracortical axon targeting are still unclear. We find that the transcription factor myocyte enhancer factor 2-c (Mef2c) directs the development of somatosensory cortical (S1) Layer 4 and 5 identity in murine postmitotic pyramidal neurons during embryogenesis. During postnatal development, expression shifts to Layer 2/3 callosal projection neurons (L2/3 CPNs). At this later developmental stage, we identify a novel function for in contralateral homotopic domain targeting by S1-L2/3 CPN axons. We employ functional manipulation of EphrinA-EphA signaling in mutant CPNs and demonstrate that Mef2c represses 6 to desensitize S1-L2/3 CPN axons to EphrinA5 repulsion at their contralateral targets. Our work uncovers dual roles for in cortical development: regulation of laminar subtype specification during embryogenesis and axon targeting in postnatal callosal neurons.

摘要

包括长程胼胝体投射在内的皮质内回路对于信息处理至关重要。大脑皮质中神经元连接的发育取决于神经元类别的有序出现,随后是特定类别的轴突投射的形成。然而,皮质内轴突靶向的遗传决定因素仍不清楚。我们发现转录因子肌细胞增强因子2-c(Mef2c)在胚胎发生过程中指导小鼠有丝分裂后锥体神经元体感皮质(S1)第4层和第5层特征的发育。在出生后发育过程中,表达转移到第2/3层胼胝体投射神经元(L2/3 CPNs)。在这个较晚的发育阶段,我们确定了其在S1-L2/3 CPN轴突对侧同位域靶向中的新功能。我们在突变的CPNs中对EphrinA-EphA信号进行功能操作,并证明Mef2c抑制6以降低S1-L2/3 CPN轴突在其对侧靶点对EphrinA5排斥的敏感性。我们的工作揭示了其在皮质发育中的双重作用:在胚胎发生过程中调节层状亚型特化以及在出生后胼胝体神经元中调节轴突靶向。

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