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皮层肌动蛋白结合蛋白2可增强微管稳定性并调节树突分支。

Cortactin-binding protein 2 increases microtubule stability and regulates dendritic arborization.

作者信息

Shih Pu-Yun, Lee Sue-Ping, Chen Yi-Kai, Hsueh Yi-Ping

机构信息

Faculty of Life Sciences, Institute of Genome Sciences, National Yang-Ming University, Taipei 112, Taiwan Institute of Molecular Biology, Academia Sinica, Taipei 115, Taiwan.

Institute of Molecular Biology, Academia Sinica, Taipei 115, Taiwan.

出版信息

J Cell Sci. 2014 Aug 15;127(Pt 16):3521-34. doi: 10.1242/jcs.149476. Epub 2014 Jun 13.

Abstract

Neurons are characterized by subcellular compartments, such as axons, dendrites and synapses, that have highly specialized morphologies and biochemical specificities. Cortactin-binding protein 2 (CTTNBP2), a neuron-specific F-actin regulator, has been shown to play a role in the regulation of dendritic spine formation and their maintenance. Here, we show that, in addition to F-actin, CTTNBP2 also associates with microtubules before mature dendritic spines form. This association of CTTNBP2 and microtubules induced the formation of microtubule bundles. Although the middle (Mid) region of CTTNBP2 was sufficient for its association with microtubules, for microtubule bundling, the N-terminal region containing the coiled-coil motifs (NCC), which mediates the dimerization or oligomerization of CTTNBP2, was also required. Our study indicates that CTTNBP2 proteins form a dimer or oligomer and brings multiple microtubule filaments together to form bundles. In cultured hippocampal neurons, knockdown of CTTNBP2 or expression of the Mid or NCC domain alone reduced the acetylation levels of microtubules and impaired dendritic arborization. This study suggests that CTTNBP2 influences both the F-actin and microtubule cytoskeletons and regulates dendritic spine formation and dendritic arborization.

摘要

神经元具有亚细胞区室,如轴突、树突和突触,它们具有高度特化的形态和生化特异性。皮层肌动蛋白结合蛋白2(CTTNBP2)是一种神经元特异性F-肌动蛋白调节剂,已被证明在树突棘的形成及其维持的调节中发挥作用。在这里,我们表明,除了F-肌动蛋白外,CTTNBP2在成熟树突棘形成之前也与微管相关联。CTTNBP2与微管的这种关联诱导了微管束的形成。尽管CTTNBP2的中间(Mid)区域足以使其与微管相关联,但对于微管束形成而言,还需要包含卷曲螺旋基序(NCC)的N端区域,该区域介导CTTNBP2的二聚化或寡聚化。我们的研究表明,CTTNBP2蛋白形成二聚体或寡聚体,并将多条微管丝聚集在一起形成束。在培养的海马神经元中,敲低CTTNBP2或单独表达Mid或NCC结构域会降低微管的乙酰化水平并损害树突分支。这项研究表明,CTTNBP2影响F-肌动蛋白和微管细胞骨架,并调节树突棘形成和树突分支。

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