Neuronal guidance behaviours: the primary cilium perspective.

IF 4.6 2区 生物学 Q2 CELL BIOLOGY
Frontiers in Cell and Developmental Biology Pub Date : 2025-06-30 eCollection Date: 2025-01-01 DOI:10.3389/fcell.2025.1612555
Melody Atkins, Coralie Fassier, Xavier Nicol
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引用次数: 0

Abstract

The establishment of functional neuronal circuits critically relies on the ability of developing neurons to accurately sense and integrate a variety of guidance signals from their surrounding environment. Such signals are indeed crucial during key steps of neuronal circuit wiring, including neuronal migration and axon guidance, to guide developing neurons or extending axons towards their target destination in the developing brain. The growth cone, located at the tip of developing neurons, is a key subcellular structure in this process, that concentrates many different guidance receptors and signalling molecules and specialises in the probing and integration of extracellular signals into various guidance behaviours. Interestingly, the small primary cilium, long considered as a vestigial organelle, has progressively emerged as a cellular antenna specialised in cell signalling, and has been reported, just like the growth cone, to harbour a variety of guidance receptors. How primary cilium-elicited signals are then transduced into specific cellular processes to guide developing neurons and axons remains however obscure. In this review, we will summarise our emerging understanding of the role of primary cilium-elicited signalling pathways on neuronal guidance processes, by focusing on neuronal migration and axon guidance. We will highlight the primary cilium molecular diversity, and how it shapes the primary cilium functional versatility, allowing the ciliary compartment to instruct various guidance behaviours through the regulation of different cellular processes. We will moreover discuss current and future avenues of research, to unravel the different molecular effectors activated downstream of specific ciliary signals, and clues to be gained from studies performed in non-neuronal cells. Rising challenges of the field will also be addressed, such as the technical challenge induced by the dual subcellular localisation (i.e., ciliary and extra-ciliary) of many ciliary guidance receptors, and the importance of the development of new genetic/chemo-genetic/optogenetic tools. Finally, we will highlight the insight such studies will bring for our understanding of the aetiology of different disorders, including ciliopathies, neurodevelopmental and neurodegenerative disorders, but also cancer cell migration/invasion, which are associated with defective primary cilium formation and function.

神经元的引导行为:初级纤毛的视角。
功能性神经元回路的建立关键依赖于发育中的神经元准确感知和整合来自周围环境的各种引导信号的能力。这些信号在神经元回路布线的关键步骤中确实是至关重要的,包括神经元迁移和轴突引导,以引导发育中的神经元或延伸轴突到达发育中的大脑中的目标目的地。生长锥位于发育中的神经元顶端,是这一过程中关键的亚细胞结构,它集中了许多不同的引导受体和信号分子,并专门探测和整合细胞外信号,以实现各种引导行为。有趣的是,小的初级纤毛,长期以来被认为是一个退化的细胞器,已经逐渐成为一个专门用于细胞信号传导的细胞天线,并且有报道称,就像生长锥一样,含有各种引导受体。然而,初级纤毛引发的信号如何被转导到特定的细胞过程中,以指导发育中的神经元和轴突,目前尚不清楚。在这篇综述中,我们将总结我们对初级纤毛引发的信号通路在神经元引导过程中的作用的新认识,重点关注神经元迁移和轴突引导。我们将重点介绍初级纤毛的分子多样性,以及它如何塑造初级纤毛的功能多样性,使纤毛室通过调节不同的细胞过程来指导各种指导行为。此外,我们将讨论当前和未来的研究途径,以揭示特定纤毛信号下游激活的不同分子效应物,以及从非神经元细胞中进行的研究中获得的线索。该领域面临的挑战也将得到解决,例如由许多纤毛引导受体的双亚细胞定位(即纤毛和纤毛外)引起的技术挑战,以及开发新的遗传/化学遗传/光遗传工具的重要性。最后,我们将强调这些研究将为我们理解不同疾病的病因学带来的见解,包括纤毛病、神经发育和神经退行性疾病,以及与初级纤毛形成和功能缺陷相关的癌细胞迁移/侵袭。
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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来源期刊
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
9.70
自引率
3.60%
发文量
2531
审稿时长
12 weeks
期刊介绍: Frontiers in Cell and Developmental Biology is a broad-scope, interdisciplinary open-access journal, focusing on the fundamental processes of life, led by Prof Amanda Fisher and supported by a geographically diverse, high-quality editorial board. The journal welcomes submissions on a wide spectrum of cell and developmental biology, covering intracellular and extracellular dynamics, with sections focusing on signaling, adhesion, migration, cell death and survival and membrane trafficking. Additionally, the journal offers sections dedicated to the cutting edge of fundamental and translational research in molecular medicine and stem cell biology. With a collaborative, rigorous and transparent peer-review, the journal produces the highest scientific quality in both fundamental and applied research, and advanced article level metrics measure the real-time impact and influence of each publication.
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