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本文引用的文献

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Neuronal microtubules: when the MAP is the roadblock.神经元微管:当微管相关蛋白成为路障时。
Trends Cell Biol. 2005 Apr;15(4):183-7. doi: 10.1016/j.tcb.2005.02.001.
2
Probing microtubule +TIPs: regulation of axon branching.探索微管正端追踪蛋白:轴突分支的调控
Curr Opin Neurobiol. 2005 Feb;15(1):58-66. doi: 10.1016/j.conb.2005.01.009.
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Linking axonal degeneration to microtubule remodeling by Spastin-mediated microtubule severing.通过Spastin介导的微管切断将轴突退变与微管重塑联系起来。
J Cell Biol. 2005 Feb 14;168(4):599-606. doi: 10.1083/jcb.200409058.
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The MAP2/Tau family of microtubule-associated proteins.微管相关蛋白的MAP2/Tau家族。
Genome Biol. 2005;6(1):204. doi: 10.1186/gb-2004-6-1-204. Epub 2004 Dec 23.
5
Role of actin filaments in the axonal transport of microtubules.肌动蛋白丝在微管轴突运输中的作用。
J Neurosci. 2004 Dec 15;24(50):11291-301. doi: 10.1523/JNEUROSCI.3443-04.2004.
6
Axonal growth is sensitive to the levels of katanin, a protein that severs microtubules.轴突生长对katanin(一种切断微管的蛋白质)的水平很敏感。
J Neurosci. 2004 Jun 23;24(25):5778-88. doi: 10.1523/JNEUROSCI.1382-04.2004.
7
Expression of the mitotic kinesin Kif15 in postmitotic neurons: implications for neuronal migration and development.有丝分裂驱动蛋白Kif15在有丝分裂后神经元中的表达:对神经元迁移和发育的影响。
J Neurocytol. 2003 Jan;32(1):79-96. doi: 10.1023/a:1027332432740.
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Slow axonal transport and the genesis of neuronal morphology.慢速轴突运输与神经元形态的形成
J Neurobiol. 2004 Jan;58(1):3-17. doi: 10.1002/neu.10281.
9
Pontocerebellar axon guidance: neuropilin-1- and semaphorin 3A-sensitivity gradients across basilar pontine nuclei and semaphorin 3A variation across cerebellum.脑桥小脑轴突导向:整个脑桥基底部核团的神经纤毛蛋白-1和3A信号蛋白敏感性梯度以及整个小脑的3A信号蛋白变异
Mol Cell Neurosci. 2002 Oct;21(2):266-84. doi: 10.1006/mcne.2002.1187.
10
Katanin-mediated microtubule severing can be regulated by multiple mechanisms.katanin介导的微管切断可通过多种机制进行调节。
Cell Motil Cytoskeleton. 2002 Dec;53(4):337-49. doi: 10.1002/cm.10080.

神经元发育过程中katanin亚基对微管切断的调控

Regulation of microtubule severing by katanin subunits during neuronal development.

作者信息

Yu Wenqian, Solowska Joanna M, Qiang Liang, Karabay Arzu, Baird Douglas, Baas Peter W

机构信息

Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, Pennsylvania 19129, USA.

出版信息

J Neurosci. 2005 Jun 8;25(23):5573-83. doi: 10.1523/JNEUROSCI.0834-05.2005.

DOI:10.1523/JNEUROSCI.0834-05.2005
PMID:15944385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1201504/
Abstract

Katanin, the microtubule-severing protein, consists of a subunit termed P60 that breaks the lattice of the microtubule and another subunit termed P80, the functions of which are not well understood. Data presented here show that the ratio of P60 to P80 varies markedly in different tissues, at different phases of development, and regionally within the neuron. P80 is more concentrated in the cell body and less variable during development, whereas P60 often shows concentrations in the distal tips of processes as well as dramatic spikes in expression at certain developmental stages. Overexpression of P60 at various stages in the differentiation of cultured hippocampal neurons results in substantial loss of microtubule mass and a diminution in total process length. In comparison, overexpression of P80, which is thought to augment the severing of microtubules by P60, results in a milder loss of microtubule mass and diminution in process length. At the developmental stage corresponding to axogenesis, overexpression of P60 decreases the total number of processes extended by the neuron, whereas overexpression of P80 produces the opposite result, suggesting that the effects on neuronal morphology are dependent on the degree of microtubule severing and loss of polymer. The microtubules that occupy the axon are notably more resistant to depolymerization in response to excess P60 or P80 than microtubules elsewhere in the neuron, suggesting that regional differences in the susceptibility of microtubules to severing proteins may be a critical factor in the generation and maintenance of neuronal polarity.

摘要

katanin,一种微管切割蛋白,由一个称为P60的亚基和另一个称为P80的亚基组成,其中P60亚基可破坏微管晶格结构,而P80亚基的功能尚不清楚。本文提供的数据表明,P60与P80的比例在不同组织、不同发育阶段以及神经元内的不同区域存在显著差异。P80在细胞体中更为集中,在发育过程中变化较小,而P60则常常在突起的远端末端富集,并且在某些发育阶段表达量会急剧上升。在培养的海马神经元分化的各个阶段过表达P60会导致微管质量大幅损失以及总突起长度缩短。相比之下,过表达P80(据认为可增强P60对微管的切割作用)会导致微管质量损失较轻且突起长度缩短程度较小。在与轴突发生相对应的发育阶段,过表达P60会减少神经元伸出的突起总数,而过表达P80则产生相反的结果,这表明对神经元形态的影响取决于微管切割程度和聚合物损失程度。与神经元其他部位的微管相比,占据轴突的微管对因过量P60或P80导致的解聚具有明显更高的抗性,这表明微管对切割蛋白敏感性的区域差异可能是神经元极性产生和维持的关键因素。