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神经纤毛蛋白-2 信号通过调节 CRMP2 来调节轴突侧支形成,从而调节癫痫大鼠模型中的苔藓纤维发芽。

Neuropilin-2 Signaling Modulates Mossy Fiber Sprouting by Regulating Axon Collateral Formation Through CRMP2 in a Rat Model of Epilepsy.

机构信息

Department of Neurology, Zhongshan Hospital, Fudan University, Shanghai, China.

Department of The State Key Laboratory of Medical Neurobiology, MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, Shanghai, China.

出版信息

Mol Neurobiol. 2022 Nov;59(11):6817-6833. doi: 10.1007/s12035-022-02995-0. Epub 2022 Aug 31.

Abstract

Programmed neural circuit formation constitutes the foundation for normal brain functions. Axon guidance cues play crucial roles in neural circuit establishment during development. Whether or how they contribute to maintaining the stability of networks in mature brains is seldom studied. Upon injury, neural rewiring could happen in adulthood, of which mossy fiber sprouting (MFS) is a canonical example. Here, we uncovered a novel role of axon guidance molecule family Sema3F/Npn-2 signaling in MFS and epileptogenesis in a rat model of epilepsy. Dentate gyrus-specific Npn-2 knockdown increased seizure activity in epileptic animals along with increased MFS. Hippocampal culture results suggested that Npn-2 signaling modulates MFS via regulating axon outgrowth and collateral formation. In addition, we discovered that Sema3F/Npn-2 signal through CRMP2 by regulating its phosphorylation in the process of MFS. Our work illustrated that Npn-2 signaling in adult epilepsy animals could potentially modulate seizure activity by controlling MFS. MFS constitutes the structural basis for abnormal electric discharge of neurons and recurrent seizures. Therapies targeting Npn-2 signaling could potentially have disease-modifying anti-epileptogenesis effects in epilepsy treatment.

摘要

程序性神经回路形成是正常大脑功能的基础。轴突导向线索在发育过程中神经回路的建立中起着至关重要的作用。它们是否以及如何有助于维持成熟大脑中网络的稳定性很少被研究。在受伤后,成年期可能会发生神经重连,其中苔藓纤维发芽(MFS)是一个典型的例子。在这里,我们在癫痫大鼠模型中发现了轴突导向分子家族 Sema3F/Npn-2 信号在 MFS 和癫痫发生中的新作用。齿状回特异性 Npn-2 敲低增加了癫痫动物的癫痫发作活动,同时增加了 MFS。海马培养结果表明,Npn-2 信号通过调节轴突生长和侧支形成来调节 MFS。此外,我们发现 Sema3F/Npn-2 通过在 MFS 过程中调节其磷酸化来通过 CRMP2 信号转导。我们的工作表明,成年癫痫动物中的 Npn-2 信号可能通过控制 MFS 来调节癫痫发作活动。MFS 是神经元异常放电和复发性癫痫的结构基础。针对 Npn-2 信号的治疗方法可能在癫痫治疗中具有改变疾病的抗癫痫发生作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e7d/9525442/a3ab470ecb3b/12035_2022_2995_Fig1_HTML.jpg

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