海马少突胶质细胞调节苔藓纤维发育参与癫痫反应。

IF 5.8 2区 医学 Q1 NEUROSCIENCES
Chunxia Jiang, Yunan Hu, Feng Zhang, Mengsheng Qiu, Xiaofeng Zhao
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引用次数: 0

摘要

虽然已知少突胶质细胞(OLs)在神经元轴突周围形成髓鞘,用于动作电位的跳跃传导,但最近的研究表明,OLs也调节神经元的功能和可塑性。在本研究中,我们发现Myrf-CKO小鼠的OL成熟缺陷引起自发性癫痫发生并导致死亡。为了进一步研究OL发育与癫痫之间的关系,我们检测了Adamts4 KO小鼠系,该小鼠系在海马中具有轻度OL分化表型。因此,突变海马的分化缺陷降低了髓磷脂相关糖蛋白的表达,并减弱了其对磷酸化原肌球蛋白相关激酶B去磷酸化的抑制作用,这与青少年海马苔藓纤维发育迟缓和成年后更易发生癫痫有关。更重要的是,通过口服clemastine增强分化,可以挽救出生后早期有缺陷的苔藓纤维发育,并减轻成人癫痫的易感性。综上所述,这些结果强烈表明,海马体中OL分化缺陷可能导致成人癫痫易感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hippocampal Oligodendrocytes Regulate Mossy Fiber Development Involved in Epileptic Responses.

Although oligodendrocytes (OLs) are known to form the myelin sheath around neuronal axons for the saltatory conduction of action potentials, recent studies have suggested that OLs also modulate neuronal function and plasticity. In the present study, we found that OL maturation deficiency in Myrf-CKO mice caused spontaneous epileptogenesis and resulted in death. To further investigate the association between OL development and epilepsy, we examined the Adamts4 KO mouse line, which has a mild OL differentiation phenotype in the hippocampus. As a result, the differentiation defect in the mutant hippocampus reduced the expression of myelin-associated glycoprotein and lessened its inhibition of the dephosphorylation of phosphorylated tropomyosin-related kinase B, which is associated with retarded adolescent hippocampal mossy fiber development and higher susceptibility to epileptogenesis in adulthood. More importantly, enhancing differentiation by orally administered clemastine rescues the defective mossy fiber development in the early postnatal period and attenuates epilepsy susceptibility in adults. Together, these results strongly suggest that an OL differentiation defect in the hippocampus may contribute to susceptibility to epilepsy in adults.

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来源期刊
Neuroscience bulletin
Neuroscience bulletin NEUROSCIENCES-
CiteScore
7.20
自引率
16.10%
发文量
163
审稿时长
6-12 weeks
期刊介绍: Neuroscience Bulletin (NB), the official journal of the Chinese Neuroscience Society, is published monthly by Shanghai Institutes for Biological Sciences (SIBS), Chinese Academy of Sciences (CAS) and Springer. NB aims to publish research advances in the field of neuroscience and promote exchange of scientific ideas within the community. The journal publishes original papers on various topics in neuroscience and focuses on potential disease implications on the nervous system. NB welcomes research contributions on molecular, cellular, or developmental neuroscience using multidisciplinary approaches and functional strategies. We feature full-length original articles, reviews, methods, letters to the editor, insights, and research highlights. As the official journal of the Chinese Neuroscience Society, which currently has more than 12,000 members in China, NB is devoted to facilitating communications between Chinese neuroscientists and their international colleagues. The journal is recognized as the most influential publication in neuroscience research in China.
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