Rho GTPase Signaling: A Molecular Switchboard for Regulating the Actin Cytoskeleton in Axon Guidance

IF 4.5 2区 生物学 Q2 CELL BIOLOGY
Madhavi Gorla, Digvijay Singh Guleria
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引用次数: 0

Abstract

Axon pathfinding is a highly dynamic process regulated by the interactions between cell-surface guidance receptors and guidance cues present in the extracellular environment. During development, precise axon pathfinding is crucial for the formation of functional neural circuits. The spatiotemporal expression of axon guidance receptors helps the navigating axon make correct decisions in a complex environment comprising both attractive and repulsive guidance cues. Axon guidance receptors initiate distinct signaling cascades that eventually influence the cytoskeleton at the growing tip of an axon, called the growth cone. The actin cytoskeleton is the primary target of these guidance signals and plays a key role in growth cone motility, exploration, and behavior. Of the many regulatory molecules that modulate the actin cytoskeleton in response to distinct guidance signals, Rho GTPases play central roles. Rho GTPases are molecular switchboards; their ON (GTP-bound) and OFF (GDP-bound) switches are controlled by their interactions with proteins that regulate the exchange of GDP for GTP or with the proteins that promote GTP hydrolysis. Various upstream signals, including axon guidance signals, regulate the activity of these Rho GTPase switch regulators. As cycling molecular switches, Rho GTPases interact with and control the activities of downstream effectors, which directly influence actin reorganization in a context-dependent manner. A deeper exploration of the spatiotemporal dynamics of Rho GTPase signaling and the molecular basis of their involvement in regulating growth cone actin cytoskeleton can unlock promising therapeutic strategies for neurodevelopmental disorders linked to dysregulated Rho GTPase signaling. This review not only provides a comprehensive overview of the field but also highlights recent discoveries that have considerably advanced our understanding of the complex regulatory roles of Rho GTPases in modulating actin cytoskeleton arrangement at the growth cone during axon guidance.

Rho GTPase信号传导:在轴突引导中调节肌动蛋白细胞骨架的分子开关板。
轴突寻路是一个高度动态的过程,受细胞表面引导受体和细胞外环境中存在的引导信号相互作用的调节。在发育过程中,精确的轴突寻路对于功能性神经回路的形成至关重要。轴突引导受体的时空表达有助于导航轴突在包含吸引和排斥引导信号的复杂环境中做出正确的决定。轴突引导受体启动不同的信号级联反应,最终影响轴突生长尖端的细胞骨架,称为生长锥。肌动蛋白细胞骨架是这些引导信号的主要目标,在生长锥运动、探索和行为中起关键作用。在许多调节肌动蛋白细胞骨架的调控分子中,Rho GTPases起着核心作用。GTPases是分子开关板;它们的ON (GTP结合)和OFF (GDP结合)开关由它们与调节GTP与GDP交换的蛋白质或促进GTP水解的蛋白质的相互作用控制。各种上游信号,包括轴突引导信号,调节这些Rho GTPase开关调节器的活性。作为循环分子开关,Rho GTPases与下游效应物相互作用并控制其活性,从而以上下文依赖的方式直接影响肌动蛋白重组。深入探索Rho GTPase信号的时空动态及其参与调节生长锥肌动蛋白细胞骨架的分子基础,可以为与Rho GTPase信号失调相关的神经发育障碍提供有希望的治疗策略。这篇综述不仅提供了该领域的全面概述,而且强调了最近的发现,这些发现大大提高了我们对Rho GTPases在轴突引导过程中调节肌动蛋白细胞骨架在生长锥上的复杂调节作用的理解。
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来源期刊
CiteScore
14.70
自引率
0.00%
发文量
256
审稿时长
1 months
期刊介绍: The Journal of Cellular Physiology publishes reports of high biological significance in areas of eukaryotic cell biology and physiology, focusing on those articles that adopt a molecular mechanistic approach to investigate cell structure and function. There is appreciation for the application of cellular, biochemical, molecular and in vivo genetic approaches, as well as the power of genomics, proteomics, bioinformatics and systems biology. In particular, the Journal encourages submission of high-interest papers investigating the genetic and epigenetic regulation of proliferation and phenotype as well as cell fate and lineage commitment by growth factors, cytokines and their cognate receptors and signal transduction pathways that influence the expression, integration and activities of these physiological mediators. Similarly, the Journal encourages submission of manuscripts exploring the regulation of growth and differentiation by cell adhesion molecules in addition to the interplay between these processes and those induced by growth factors and cytokines. Studies on the genes and processes that regulate cell cycle progression and phase transition in eukaryotic cells, and the mechanisms that determine whether cells enter quiescence, proliferate or undergo apoptosis are also welcomed. Submission of papers that address contributions of the extracellular matrix to cellular phenotypes and physiological control as well as regulatory mechanisms governing fertilization, embryogenesis, gametogenesis, cell fate, lineage commitment, differentiation, development and dynamic parameters of cell motility are encouraged. Finally, the investigation of stem cells and changes that differentiate cancer cells from normal cells including studies on the properties and functions of oncogenes and tumor suppressor genes will remain as one of the major interests of the Journal.
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