轴突初段可塑性中的肌动蛋白聚合和纵向肌动蛋白纤维

IF 3.5 3区 医学 Q2 NEUROSCIENCES Frontiers in Molecular Neuroscience Pub Date : 2024-05-10 DOI:10.3389/fnmol.2024.1376997
David Micinski, Pirta Hotulainen
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引用次数: 0

摘要

轴突起始节段(AIS)位于神经元的体节和轴突之间的交界处,因此在维持神经极性和作为动作电位产生的场所方面起着重要作用。轴突初段还能以活动依赖的方式进行大规模迁移。这代表了一种同态可塑性,神经元通过改变 AIS 的大小和/或位置来调节自身的兴奋性。虽然 AIS 可塑性对含 AIS 神经元的正常功能非常重要,但人们对 AIS 可塑性的细胞和分子机制却知之甚少。在这里,我们利用三维结构照明显微镜(3D-SIM)分析了 AIS 可塑性过程中 AIS 肌动蛋白细胞骨架的变化。我们发现,在可塑性诱导 3 小时后,纵向肌动蛋白纤维的数量瞬时增加。我们进一步发现,肌动蛋白聚合,尤其是甲形蛋白介导的肌动蛋白聚合,是AIS可塑性和纵向肌动蛋白纤维形成所必需的。在形蛋白家族中,Daam1定位于纵向肌动蛋白纤维的末端。这些结果表明,肌动蛋白细胞骨架的主动重组是AIS正常可塑性所必需的。
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Actin polymerization and longitudinal actin fibers in axon initial segment plasticity
The location of the axon initial segment (AIS) at the junction between the soma and axon of neurons makes it instrumental in maintaining neural polarity and as the site for action potential generation. The AIS is also capable of large-scale relocation in an activity-dependent manner. This represents a form of homeostatic plasticity in which neurons regulate their own excitability by changing the size and/or position of the AIS. While AIS plasticity is important for proper functionality of AIS-containing neurons, the cellular and molecular mechanisms of AIS plasticity are poorly understood. Here, we analyzed changes in the AIS actin cytoskeleton during AIS plasticity using 3D structured illumination microscopy (3D-SIM). We showed that the number of longitudinal actin fibers increased transiently 3 h after plasticity induction. We further showed that actin polymerization, especially formin mediated actin polymerization, is required for AIS plasticity and formation of longitudinal actin fibers. From the formin family of proteins, Daam1 localized to the ends of longitudinal actin fibers. These results indicate that active re-organization of the actin cytoskeleton is required for proper AIS plasticity.
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来源期刊
CiteScore
5.70
自引率
2.10%
发文量
669
审稿时长
14 weeks
期刊介绍: Frontiers in Molecular Neuroscience is a first-tier electronic journal devoted to identifying key molecules, as well as their functions and interactions, that underlie the structure, design and function of the brain across all levels. The scope of our journal encompasses synaptic and cellular proteins, coding and non-coding RNA, and molecular mechanisms regulating cellular and dendritic RNA translation. In recent years, a plethora of new cellular and synaptic players have been identified from reduced systems, such as neuronal cultures, but the relevance of these molecules in terms of cellular and synaptic function and plasticity in the living brain and its circuits has not been validated. The effects of spine growth and density observed using gene products identified from in vitro work are frequently not reproduced in vivo. Our journal is particularly interested in studies on genetically engineered model organisms (C. elegans, Drosophila, mouse), in which alterations in key molecules underlying cellular and synaptic function and plasticity produce defined anatomical, physiological and behavioral changes. In the mouse, genetic alterations limited to particular neural circuits (olfactory bulb, motor cortex, cortical layers, hippocampal subfields, cerebellum), preferably regulated in time and on demand, are of special interest, as they sidestep potential compensatory developmental effects.
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