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本文引用的文献

1
MAP2d mRNA is expressed in identified neuronal populations in the developing and adult rat brain and its subcellular distribution differs from that of MAP2b in hippocampal neurones.微管相关蛋白2d(MAP2d)信使核糖核酸(mRNA)在发育中和成年大鼠大脑中已确定的神经元群体中表达,并且其亚细胞分布与海马神经元中的微管相关蛋白2b(MAP2b)不同。
Eur J Neurosci. 1998 Jan;10(1):161-71. doi: 10.1046/j.1460-9568.1998.00044.x.
2
Expression of the mitotic motor protein CHO1/MKLP1 in postmitotic neurons.有丝分裂运动蛋白CHO1/MKLP1在有丝分裂后神经元中的表达。
Eur J Neurosci. 1998 Apr;10(4):1383-93. doi: 10.1046/j.1460-9568.1998.00159.x.
3
Interstitial branches develop from active regions of the axon demarcated by the primary growth cone during pausing behaviors.在暂停行为期间,间质分支从由初级生长锥划定的轴突活跃区域发育而来。
J Neurosci. 1998 Oct 1;18(19):7930-40. doi: 10.1523/JNEUROSCI.18-19-07930.1998.
4
Cytoplasmic dynein and dynactin are required for the transport of microtubules into the axon.细胞质动力蛋白和动力蛋白激活蛋白是微管向轴突运输所必需的。
J Cell Biol. 1998 Jan 26;140(2):391-401. doi: 10.1083/jcb.140.2.391.
5
The mechanisms of fast and slow transport in neurons: identification and characterization of the new kinesin superfamily motors.神经元中快速和慢速运输的机制:新型驱动蛋白超家族马达的鉴定与表征
Curr Opin Neurobiol. 1997 Oct;7(5):605-14. doi: 10.1016/s0959-4388(97)80079-7.
6
Identification and classification of 16 new kinesin superfamily (KIF) proteins in mouse genome.小鼠基因组中16种新的驱动蛋白超家族(KIF)蛋白的鉴定与分类。
Proc Natl Acad Sci U S A. 1997 Sep 2;94(18):9654-9. doi: 10.1073/pnas.94.18.9654.
7
The bimC family of kinesins: essential bipolar mitotic motors driving centrosome separation.驱动蛋白的bimC家族:驱动中心体分离的必需双极有丝分裂马达蛋白
Biochim Biophys Acta. 1997 Jul 24;1357(3):257-71. doi: 10.1016/s0167-4889(97)00037-2.
8
Identification of a microtubule-associated motor protein essential for dendritic differentiation.鉴定一种对树突分化至关重要的微管相关运动蛋白。
J Cell Biol. 1997 Aug 25;138(4):833-43. doi: 10.1083/jcb.138.4.833.
9
Immunodetection of cytoskeletal structures and the Eg5 motor protein on deep-etch replicas of Xenopus egg cortices isolated during the cortical rotation.
Biol Cell. 1996;88(3):89-98.
10
FGF-2 induces nerve growth factor expression in cultured rat hippocampal neurons.
Eur J Neurosci. 1997 Jun;9(6):1282-9. doi: 10.1111/j.1460-9568.1997.tb01483.x.

有丝分裂运动蛋白Eg5在有丝分裂后神经元中的表达:对神经元发育的影响。

Expression of the mitotic motor protein Eg5 in postmitotic neurons: implications for neuronal development.

作者信息

Ferhat L, Cook C, Chauviere M, Harper M, Kress M, Lyons G E, Baas P W

机构信息

Department of Anatomy, The University of Wisconsin Medical School, Madison, Wisconsin 53706, USA.

出版信息

J Neurosci. 1998 Oct 1;18(19):7822-35. doi: 10.1523/JNEUROSCI.18-19-07822.1998.

DOI:10.1523/JNEUROSCI.18-19-07822.1998
PMID:9742151
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6793023/
Abstract

It is well established that the microtubules of the mitotic spindle are organized by a variety of motor proteins, and it appears that the same motors or closely related variants organize microtubules in the postmitotic neuron. Specifically, cytoplasmic dynein and the kinesin-related motor known as CHO1/MKLP1 are used within the mitotic spindle, and recent studies suggest that they are also essential for the establishment of the axonal and dendritic microtubule arrays of the neuron. Other motors are required to tightly regulate microtubule behaviors in the mitotic spindle, and it is attractive to speculate that these motors might also help to regulate microtubule behaviors in the neuron. Here we show that a homolog of the mitotic kinesin-related motor known as Eg5 continues to be expressed in rodent neurons well after their terminal mitotic division. In neurons, Eg5 is directly associated with the microtubule array and is enriched within the distal regions of developing processes. This distal enrichment is transient, and typically lost after a process has been clearly defined as an axon or a dendrite. Strong expression can resume later in development, and if so, the protein concentrates within newly forming sprouts at the distal tips of dendrites. We suggest that Eg5 generates forces that help to regulate microtubule behaviors within the distal tips of developing axons and dendrites.

摘要

有充分证据表明,有丝分裂纺锤体的微管是由多种驱动蛋白组织起来的,而且看起来同样的驱动蛋白或密切相关的变体在有丝分裂后的神经元中组织微管。具体而言,胞质动力蛋白和名为CHO1/MKLP1的驱动蛋白相关分子马达在有丝分裂纺锤体中发挥作用,最近的研究表明,它们对于神经元轴突和树突微管阵列的形成也至关重要。其他驱动蛋白对于紧密调控有丝分裂纺锤体中的微管行为是必需的,推测这些驱动蛋白可能也有助于调控神经元中的微管行为很有吸引力。在此我们表明,名为Eg5的有丝分裂驱动蛋白相关分子马达的一个同源物在啮齿动物神经元终末有丝分裂后很长时间仍持续表达。在神经元中,Eg5直接与微管阵列相关联,并在发育中突起的远端区域富集。这种远端富集是短暂的,通常在一个突起被明确界定为轴突或树突后消失。在发育后期,强表达可能会恢复,如果是这样,该蛋白会集中在树突远端新形成的芽中。我们认为,Eg5产生有助于调控发育中轴突和树突远端微管行为的力。