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局部mRNA翻译与细胞骨架重组:调节神经元反应的机制。

Local mRNA translation and cytoskeletal reorganization: Mechanisms that tune neuronal responses.

作者信息

Triantopoulou Nikoletta, Vidaki Marina

机构信息

Division of Basic Sciences, Medical School, University of Crete, Heraklion, Greece.

Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology Hellas (IMBB-FORTH), Heraklion, Greece.

出版信息

Front Mol Neurosci. 2022 Aug 1;15:949096. doi: 10.3389/fnmol.2022.949096. eCollection 2022.

Abstract

Neurons are highly polarized cells with significantly long axonal and dendritic extensions that can reach distances up to hundreds of centimeters away from the cell bodies in higher vertebrates. Their successful formation, maintenance, and proper function highly depend on the coordination of intricate molecular networks that allow axons and dendrites to quickly process information, and respond to a continuous and diverse cascade of environmental stimuli, often without enough time for communication with the soma. Two seemingly unrelated processes, essential for these rapid responses, and thus neuronal homeostasis and plasticity, are local mRNA translation and cytoskeletal reorganization. The axonal cytoskeleton is characterized by high stability and great plasticity; two contradictory attributes that emerge from the powerful cytoskeletal rearrangement dynamics. Cytoskeletal reorganization is crucial during nervous system development and in adulthood, ensuring the establishment of proper neuronal shape and polarity, as well as regulating intracellular transport and synaptic functions. Local mRNA translation is another mechanism with a well-established role in the developing and adult nervous system. It is pivotal for axonal guidance and arborization, synaptic formation, and function and seems to be a key player in processes activated after neuronal damage. Perturbations in the regulatory pathways of local translation and cytoskeletal reorganization contribute to various pathologies with diverse clinical manifestations, ranging from intellectual disabilities (ID) to autism spectrum disorders (ASD) and schizophrenia (SCZ). Despite the fact that both processes are essential for the orchestration of pathways critical for proper axonal and dendritic function, the interplay between them remains elusive. Here we review our current knowledge on the molecular mechanisms and specific interaction networks that regulate and potentially coordinate these interconnected processes.

摘要

神经元是高度极化的细胞,具有显著长的轴突和树突延伸,在高等脊椎动物中,这些延伸可到达距离细胞体数百厘米远的地方。它们的成功形成、维持和正常功能高度依赖于复杂分子网络的协调,这些网络使轴突和树突能够快速处理信息,并对连续多样的环境刺激级联做出反应,而通常没有足够的时间与胞体进行通信。对于这些快速反应以及神经元的稳态和可塑性至关重要的两个看似不相关的过程是局部mRNA翻译和细胞骨架重组。轴突细胞骨架的特点是高稳定性和高可塑性;这两个相互矛盾的特性源于强大的细胞骨架重排动力学。细胞骨架重组在神经系统发育和成年期都至关重要,它确保了适当的神经元形状和极性的建立,以及调节细胞内运输和突触功能。局部mRNA翻译是另一种在发育中和成年神经系统中具有既定作用的机制。它对于轴突导向和分支、突触形成及功能至关重要,并且似乎是神经元损伤后激活的过程中的关键参与者。局部翻译和细胞骨架重组的调节途径的扰动会导致各种具有不同临床表现的病理状况,从智力残疾(ID)到自闭症谱系障碍(ASD)和精神分裂症(SCZ)。尽管这两个过程对于协调对轴突和树突正常功能至关重要的途径都是必不可少的,但它们之间的相互作用仍然难以捉摸。在这里,我们综述了我们目前关于调节并可能协调这些相互关联过程的分子机制和特定相互作用网络的知识。

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