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Wnt7b通过调节JNK介导的细胞骨架动力学促进轴突分化和延伸。

Wnt7b Promotes Axon Differentiation and Extension by Regulating JNK-Mediated Cytoskeletal Dynamics.

作者信息

Neila Lorena P, Luna Sebastian, Vena Rodrigo, Rosso Silvana B

机构信息

Área Toxicología. Departamento de Ciencias de los Alimentos y Medio Ambiente, Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario, Suipacha 531, S2002LRK, Rosario, Santa Fe, Argentina.

Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Rosario, Argentina.

出版信息

Neurochem Res. 2025 Sep 4;50(5):284. doi: 10.1007/s11064-025-04540-6.

DOI:10.1007/s11064-025-04540-6
PMID:40906300
Abstract

Neuronal polarization and axon growth are critical processes underlying neuronal differentiation and maturation. Wnt proteins have been implicated as key regulators of neuronal development; however, the cellular mechanisms through which they influence axon growth remain poorly understood. In this study, we investigated the role of Wnt7b in axon differentiation and elongation in hippocampal neurons, and aimed to characterize the underlying molecular mechanisms involved. Our results show that Wnt7b accelerates neuronal polarization and promotes axon elongation. In the presence of Wnt7b, most undifferentiated neurons polarized and subsequently developed longer axons compared to controls. Further analysis revealed that this effect is mediated by the JNK signaling pathway, as both pharmacological inhibition and expression of a dominant-negative JNK construct blocked Wnt7b-induced axonal elongation. Additionally, Wnt7b triggered local activation of JNK in growing axons and induced cytoskeletal rearrangements. Specially, Wnt stimulation promoted microtubule stabilization along newly formed axons and enhanced the protrusion of dynamic microtubules into the growth cones, a process that may facilitate axon extension. Together, these findings identify Wnt7b as a crucial modulator of axon differentiation and elongation, acting through activation of the JNK pathway.

摘要

神经元极化和轴突生长是神经元分化和成熟的关键过程。Wnt蛋白被认为是神经元发育的关键调节因子;然而,它们影响轴突生长的细胞机制仍知之甚少。在本研究中,我们研究了Wnt7b在海马神经元轴突分化和伸长中的作用,旨在阐明其潜在的分子机制。我们的结果表明,Wnt7b加速神经元极化并促进轴突伸长。与对照组相比,在Wnt7b存在的情况下,大多数未分化的神经元发生极化并随后长出更长的轴突。进一步分析表明,这种作用是由JNK信号通路介导的,因为药理学抑制和显性负性JNK构建体的表达均阻断了Wnt7b诱导的轴突伸长。此外,Wnt7b触发生长轴突中JNK的局部激活并诱导细胞骨架重排。特别地,Wnt刺激促进新形成轴突上微管的稳定,并增强动态微管向生长锥的突出,这一过程可能有助于轴突延伸。总之,这些发现确定Wnt7b是轴突分化和伸长的关键调节因子,通过激活JNK途径发挥作用。

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本文引用的文献

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A genetic variant of the Wnt receptor LRP6 accelerates synapse degeneration during aging and in Alzheimer's disease.LRP6 这个 Wnt 受体的一个遗传变异体在衰老和阿尔茨海默病期间加速了突触退化。
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