Axonal transport of neurofilaments in normal and disease states

被引:75
作者
Miller, CCJ
Ackerley, S
Brownlees, J
Grierson, AJ
Jacobsen, NJO
Thornhill, P
机构
[1] Kings Coll London, Inst Phys, Dept Neurosci, London SE5 8AF, England
[2] Kings Coll London, Inst Phys, Dept Neurol, London SE5 8AF, England
基金
英国医学研究理事会;
关键词
neurofilaments; phosphorylation; amyotrophic lateral sclerosis; Alzheimer's disease; Parkinson's disease; axonal transport;
D O I
10.1007/s00018-002-8425-7
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 among the most abundant organelles in neurones. They are synthesised in cell bodies and then transported into and through axons by a process termed 'slow axonal transport' at a rate that is distinct from that driven by conventional fast motors. Several recent studies have now demonstrated that this slow rate of transport is actually the consequence of conventional fast rates of movement that are interrupted by extended pausing. At any one time, most neurofilaments are thus stationary. Accumulations of neurofilaments are a pathological feature of several human neurodegenerative diseases suggesting that neurofilament transport is disrupted in disease states. Here, we review recent advances in our understanding of neurofilament transport in both normal and disease states. Increasing evidence suggests that phosphorylation of neurofilaments is a mechanism for regulating their transport properties, possibly by promoting their detachment from the motor(s). In some neuro degenerative diseases, signal transduction mechanisms involving neurofilament kinases and phosphatases may be perturbed leading to disruption of transport.
引用
收藏
页码:323 / 330
页数:8
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