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卷曲蛋白 5 受体参与海马神经元的神经元极性和形态发生。

Frizzled-5 receptor is involved in neuronal polarity and morphogenesis of hippocampal neurons.

机构信息

Centro de Envejecimiento y Regeneración (CARE), Departamento de Biología Celular y Molecular, Facultad de Ciencias Biológicas, P. Universidad Católica de Chile, Santiago, Chile.

出版信息

PLoS One. 2013 Oct 18;8(10):e78892. doi: 10.1371/journal.pone.0078892. eCollection 2013.

Abstract

The Wnt signaling pathway plays important roles during different stages of neuronal development, including neuronal polarization and dendritic and axonal outgrowth. However, little is known about the identity of the Frizzled receptors mediating these processes. In the present study, we investigated the role of Frizzled-5 (Fzd5) on neuronal development in cultured Sprague-Dawley rat hippocampal neurons. We found that Fzd5 is expressed early in cultured neurons on actin-rich structures localized at minor neurites and axonal growth cones. At 4 DIV, Fzd5 polarizes towards the axon, where its expression is detected mainly at the peripheral zone of axonal growth cones, with no obvious staining at dendrites; suggesting a role of Fzd5 in neuronal polarization. Overexpression of Fzd5 during the acquisition of neuronal polarity induces mislocalization of the receptor and a loss of polarized axonal markers. Fzd5 knock-down leads to loss of axonal proteins, suggesting an impaired neuronal polarity. In contrast, overexpression of Fzd5 in neurons that are already polarized did not alter polarity, but decreased the total length of axons and increased total dendrite length and arborization. Fzd5 activated JNK in HEK293 cells and the effects triggered by Fzd5 overexpression in neurons were partially prevented by inhibition of JNK, suggesting that a non-canonical Wnt signaling mechanism might be involved. Our results suggest that, Fzd5 has a role in the establishment of neuronal polarity, and in the morphogenesis of neuronal processes, in part through the activation of the non-canonical Wnt mechanism involving JNK.

摘要

Wnt 信号通路在神经元发育的不同阶段发挥重要作用,包括神经元极化、树突和轴突生长。然而,介导这些过程的卷曲受体的身份知之甚少。在本研究中,我们研究了卷曲受体 5(Fzd5)在培养的 Sprague-Dawley 大鼠海马神经元发育中的作用。我们发现 Fzd5 在培养神经元中的早期表达,位于 actin 丰富的结构上,定位于小神经突和轴突生长锥。在 4 天体外培养(DIV)时,Fzd5 向轴突极化,其表达主要在轴突生长锥的外周区检测到,在树突中没有明显染色;提示 Fzd5 在神经元极化中的作用。在获得神经元极性期间过表达 Fzd5 会导致受体定位错误,并丧失极化的轴突标记物。Fzd5 敲低会导致轴突蛋白丢失,提示神经元极性受损。相比之下,在已经极化的神经元中过表达 Fzd5 不会改变极性,但会减少轴突的总长度,增加总树突长度和分支。Fzd5 在 HEK293 细胞中激活 JNK,并且 Fzd5 在神经元中的过表达引发的效应部分被 JNK 抑制所阻止,提示可能涉及非经典 Wnt 信号机制。我们的结果表明,Fzd5 在神经元极性的建立和神经元过程的形态发生中起作用,部分通过激活涉及 JNK 的非经典 Wnt 机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c55a/3800132/a8b8cb3de617/pone.0078892.g001.jpg

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