Regulation of EB1/3 proteins by classical MAPs in neurons.

Bioarchitecture Pub Date : 2014-01-01 Epub Date: 2014-01-10 DOI:10.4161/bioa.27774
C L Sayas, Jesús Avila
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引用次数: 13

Abstract

Microtubules (MTs) are key cytoskeletal elements in developing and mature neurons. MT reorganization underlies the morphological changes that occur during neuronal development. Furthermore, MTs contribute to the maintenance of neuronal architecture, enable intracellular transport and act as scaffolds for signaling molecules. Thus, a fine-tuned regulation of MT dynamics and stability is crucial for the correct differentiation and functioning of neurons. Different types of proteins contribute to the regulation of the MT state, such as plus-end tracking proteins (+TIPs), which interact with the plus-ends of growing microtubules, and classical microtubule-associated proteins (MAPs), which bind along the microtubule lattice. Recent evidence indicates that MAPs interplay with End Binding Proteins (EBs), the core +TIPs, in neuronal cells. This might contribute to the orchestrated regulation of MT dynamics in neurons. In this mini-review article, we address recent research on the neuronal crosstalk between EBs and classical MAPs and speculate on its possible functional relevance.

Abstract Image

经典map对神经元中EB1/3蛋白的调控。
微管(MTs)是发育和成熟神经元的关键细胞骨架元件。MT重组是神经元发育过程中发生的形态学变化的基础。此外,mt有助于维持神经元结构,使细胞内运输和作为信号分子的支架。因此,MT动力学和稳定性的精细调节对于神经元的正确分化和功能至关重要。不同类型的蛋白质有助于调控MT状态,例如与生长微管的正端相互作用的正端跟踪蛋白(+TIPs),以及沿着微管晶格结合的经典微管相关蛋白(MAPs)。最近的证据表明,在神经细胞中,map与末端结合蛋白(End Binding Proteins, EBs),即核心+TIPs相互作用。这可能有助于神经元中MT动力学的协调调节。在这篇小型综述文章中,我们讨论了EBs和经典map之间的神经元串扰的最新研究,并推测其可能的功能相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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