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微管细胞骨架在神经发育障碍中的作用。

The Role of the Microtubule Cytoskeleton in Neurodevelopmental Disorders.

作者信息

Lasser Micaela, Tiber Jessica, Lowery Laura Anne

机构信息

Department of Biology, Boston College, Chestnut Hill, MA, United States.

出版信息

Front Cell Neurosci. 2018 Jun 14;12:165. doi: 10.3389/fncel.2018.00165. eCollection 2018.

Abstract

Neurons depend on the highly dynamic microtubule (MT) cytoskeleton for many different processes during early embryonic development including cell division and migration, intracellular trafficking and signal transduction, as well as proper axon guidance and synapse formation. The coordination and support from MTs is crucial for newly formed neurons to migrate appropriately in order to establish neural connections. Once connections are made, MTs provide structural integrity and support to maintain neural connectivity throughout development. Abnormalities in neural migration and connectivity due to genetic mutations of MT-associated proteins can lead to detrimental developmental defects. Growing evidence suggests that these mutations are associated with many different neurodevelopmental disorders, including intellectual disabilities (ID) and autism spectrum disorders (ASD). In this review article, we highlight the crucial role of the MT cytoskeleton in the context of neurodevelopment and summarize genetic mutations of various MT related proteins that may underlie or contribute to neurodevelopmental disorders.

摘要

在胚胎早期发育的许多不同过程中,神经元依赖高度动态的微管(MT)细胞骨架,这些过程包括细胞分裂和迁移、细胞内运输和信号转导,以及正确的轴突导向和突触形成。微管的协调和支持对于新形成的神经元进行适当迁移以建立神经连接至关重要。一旦建立连接,微管在整个发育过程中提供结构完整性和支持以维持神经连接。由于微管相关蛋白的基因突变导致的神经迁移和连接异常可导致有害的发育缺陷。越来越多的证据表明,这些突变与许多不同的神经发育障碍有关,包括智力障碍(ID)和自闭症谱系障碍(ASD)。在这篇综述文章中,我们强调了微管细胞骨架在神经发育背景下的关键作用,并总结了各种与微管相关蛋白的基因突变,这些突变可能是神经发育障碍的基础或促成因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28a0/6010848/149aba3d6e96/fncel-12-00165-g0001.jpg

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