Deregulation of PKN1 activity disrupts neurofilament organisation and axonal transport

被引:32
|
作者
Manser, Catherine [1 ]
Stevenson, Alison [1 ]
Banner, Steven [1 ]
Davies, Jennifer [1 ]
Tudor, Elizabeth L. [1 ]
Ono, Yoshitaka [2 ]
Leigh, P. Nigel [1 ]
McLoughlin, Declan M. [1 ]
Shaw, Christopher E. [1 ]
Miller, Christopher C. J. [1 ]
机构
[1] Kings Coll London, Inst Psychiat, Dept Neurosci P037, MRC Ctr Neurodegenerat Res, London SE5 8AF, England
[2] Kobe Univ, Biosignal Res Ctr, Kobe, Hyogo 6578501, Japan
基金
英国医学研究理事会; 英国惠康基金;
关键词
neurofilament; PKN; axonal transport; amyotrophic lateral sclerosis; motor neuron disease;
D O I
10.1016/j.febslet.2008.05.034
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neurofilaments are synthesised in neuronal cell bodies and then transported through axons. Damage to neurofilament transport is seen in amyotrophic lateral sclerosis (ALS). Here, we show that PKN1, a neurofilament head-rod domain kinase is cleaved and activated in SOD1G93A transgenic mice that are a model of ALS. Moreover, we demonstrate that glutamate, a proposed toxic mechanism in ALS leads to caspase cleavage and disruption of PKN1 in neurons. Finally, we demonstrate that a cleaved form of PKN1 but not wild-type PKN1 disrupts neurofilament organisation and axonal transport. Thus, deregulation of PKN1 may contribute to the pathogenic process in ALS. (C) 2008 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2303 / 2308
页数:6
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