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深入了解皮质发育全局和局灶性迁移障碍的发育机制。

Insight into developmental mechanisms of global and focal migration disorders of cortical development.

机构信息

Department of Neurosciences, Division of Child Neurology, University of California San Diego, San Diego, CA, USA.

Department of Neurosciences, Rady Children's Institute for Genomic Medicine, University of California San Diego, San Diego, CA, USA.

出版信息

Curr Opin Neurobiol. 2021 Feb;66:77-84. doi: 10.1016/j.conb.2020.10.005. Epub 2020 Oct 21.

Abstract

Cortical development involves neurogenesis followed by migration, maturation, and myelination of immature neurons. Disruptions in these processes can cause malformations of cortical development (MCD). Radial glia (RG) are the stem cells of the brain, both generating neurons and providing the scaffold upon which immature neurons radially migrate. Germline mutations in genes required for cell migration, or cell-cell contact, often lead to global MCDs. Somatic mutations in RG in genes involved in homeostatic function, like mTOR signaling, often lead to focal MCDs. Two different mutations occurring in the same patient can combine in ways we are just beginning to understand. Our growing knowledge about MCD suggests mTOR inhibitors may have expanded utility in treatment-resistant epilepsy, while imaging techniques can better delineate the type and extent of these lesions.

摘要

皮质发育涉及神经发生,随后是不成熟神经元的迁移、成熟和髓鞘形成。这些过程的中断会导致皮质发育畸形(MCD)。放射状胶质(RG)是大脑的干细胞,既能产生神经元,又能为不成熟神经元的放射状迁移提供支架。细胞迁移或细胞间接触所需基因的种系突变,常导致广泛的 MCD。涉及同源性功能的 RG 基因中的体细胞突变,如 mTOR 信号通路,常导致局灶性 MCD。同一患者中发生的两种不同突变可能以我们才刚刚开始理解的方式组合。我们对 MCD 的认识不断加深,提示 mTOR 抑制剂在治疗耐药性癫痫方面可能具有更广泛的应用,而影像学技术可以更好地描绘这些病变的类型和范围。

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