The potential role of cyclin-dependent kinase 5 in focal cortical dysplasia

被引:10
|
作者
Sen, Arjune
Thom, Maria [1 ]
Nikolic, Margareta [2 ]
Sisodiya, Sanjay M.
机构
[1] UCL, Neurol Inst, Div Neuropathol, London, England
[2] Imperial Coll Sch Med, Fac Med, Dept Cellular & Mol Neurosci, London, England
基金
英国惠康基金;
关键词
cyclin-dependent kinase 5; epilepsy; focal cortical; dysplasia; p35; reelin;
D O I
10.1159/000109855
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Focal cortical dysplasia (FCD) is the most common malformation of cortical development found in epilepsy surgical series. Characterised by cortical mislamination, dysplastic neurons and, in a subgroup of cases, balloon cells, FCD is potently epileptogenic. Despite decades of study, the underlying aetiology of FCD remains uncertain and research has been hampered by the lack of a good animal model in which to simulate the condition. In this article we review some of the potential molecular mechanisms that might underpin human FCD. In particular we examine the potential role of cyclin-dependent kinase 5 and its principal activator p35 in FCD and estimate the contribution that deregulation of cyclin-dependent kinase 5 might make to the pathogenesis of this condition. Copyright (c) 2008 S. Karger AG, Basel.
引用
收藏
页码:96 / 104
页数:9
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