Focal cortical dysplasia: a neuropathological and developmental perspective

被引:29
作者
Cotter, DR [1 ]
Honavar, M [1 ]
Everall, I [1 ]
机构
[1] Inst Psychiat, Dept Neuropathol, Sect Clin Neuropharmacol, London SE5 8AF, England
基金
英国医学研究理事会;
关键词
differentiation; epilepsy; focal cortical dysplasia; neuronal migration;
D O I
10.1016/S0920-1211(99)00049-2
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Focal cortical dysplasia (FCD) is a rare, sporadic disorder which is a recognised cause of chronic epilepsy. It is proposed to result from disordered neuronal migration and differentiation and has characteristic histological features which include disturbed cortical lamination, large abnormal neurons and the presence of large balloon cells with glassy eosinophilic cytoplasm and pleomorphic eccentric nuclei. These latter express both glial and neuronal markers indicative of abnormal neuroglial differentiation. In this paper we review the current literature on the neuropathology of FCD and discuss potential mechanisms. We focus on growth factors, signalling pathways and candidate genes with known roles in Drosophila and vertebrate brain development that could be responsible for the developmental brain changes seen in FCD. At issue are the factors that influence cell fate and differentiation and which regulate neural migration. Some of the molecular pathways, such as those involving the Notch and the Wnt pathways have particularly important roles in neuroglial differentiation in vertebrates, and these are proposed as potential candidates. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:155 / 164
页数:10
相关论文
共 63 条
[31]   Notch signalling - A short cut to the nucleus [J].
Lewis, J .
NATURE, 1998, 393 (6683) :304-305
[32]   Neural progenitors and stem cells: mechanisms of progenitor heterogeneity [J].
Lillien, L .
CURRENT OPINION IN NEUROBIOLOGY, 1998, 8 (01) :37-44
[33]   MASH1 maintains competence for BMP2-induced neuronal differentiation in post-migratory neural crest cells [J].
Lo, LC ;
Sommer, L ;
Anderson, DJ .
CURRENT BIOLOGY, 1997, 7 (06) :440-450
[34]  
LUSKIN MB, 1993, J NIH RES, V5, P60
[35]   CONSIDERATIONS ON THE SIGNIFICANCE ATTRIBUTED TO UNUSUAL CEREBRAL HISTOLOGICAL-FINDINGS RECENTLY DESCRIBED IN 8 PATIENTS WITH PRIMARY GENERALIZED EPILEPSY [J].
LYON, G ;
GASTAUT, H .
EPILEPSIA, 1985, 26 (04) :365-367
[36]   Identification of neurogenin, a vertebrate neuronal determination gene [J].
Ma, QF ;
Kintner, C ;
Anderson, DJ .
CELL, 1996, 87 (01) :43-52
[37]  
MAROULAKOU IG, 1994, ONCOGENE, V9, P1551
[38]   CONSTRUCTING THE CEREBRAL-CORTEX - NEUROGENESIS AND FATE DETERMINATION [J].
MCCONNELL, SK .
NEURON, 1995, 15 (04) :761-768
[39]   CELL-CYCLE DEPENDENCE OF LAMINAR DETERMINATION IN DEVELOPING NEOCORTEX [J].
MCCONNELL, SK ;
KAZNOWSKI, CE .
SCIENCE, 1991, 254 (5029) :282-285
[40]   SPECIFICATION OF THE ANTEROPOSTERIOR NEURAL AXIS THROUGH SYNERGISTIC INTERACTION OF THE WNT SIGNALING CASCADE WITH NOGGIN AND FOLLISTATIN [J].
MCGREW, LL ;
LAI, CJ ;
MOON, RT .
DEVELOPMENTAL BIOLOGY, 1995, 172 (01) :337-342