DENDRITIC MORPHOLOGY IN EPILEPTOGENIC CORTEX FROM TRPE PATIENTS, REVEALED BY INTRACELLULAR LUCIFER-YELLOW MICROINJECTION AND CONFOCAL LASER-SCANNING MICROSCOPY

被引:29
作者
BELICHENKO, PV
SOURANDER, P
MALMGREN, K
NORDBORG, C
HEDSTROM, A
VONESSEN, C
RYDENHAG, B
LINDSTROM, S
UVEBRANT, P
DAHLSTROM, A
机构
[1] GOTHENBURG UNIV,INST NEUROBIOL,DEPT ANAT & CELL BIOL,S-41390 GOTHENBURG,SWEDEN
[2] RUSSIAN ACAD MED SCI,INST BRAIN RES,MOSCOW,RUSSIA
[3] GOTHENBURG UNIV,FAC MED,DEPT PATHOL,DIV NEUROPATHOL,GOTHENBURG,SWEDEN
[4] GOTHENBURG UNIV,FAC MED,DEPT NEUROL,GOTHENBURG,SWEDEN
[5] GOTHENBURG UNIV,FAC MED,DEPT NEUROSURG,GOTHENBURG,SWEDEN
[6] GOTHENBURG UNIV,FAC MED,DEPT NEUROPHYSIOL,GOTHENBURG,SWEDEN
[7] GOTHENBURG UNIV,FAC MED,DEPT CLIN NEUROPHYSIOL,GOTHENBURG,SWEDEN
[8] GOTHENBURG UNIV,FAC MED,DEPT PEDIAT,GOTHENBURG,SWEDEN
关键词
MICRODYSGENESIS; DENDRITIC MORPHOLOGY; INTRACELLULAR STAINING; LUCIFER YELLOW; CONFOCAL MICROSCOPY;
D O I
10.1016/0920-1211(94)90044-2
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Biopsy material was obtained from cortical epileptogenic zones (eight temporal, one occipital, one parietal and one frontal) of eleven patients aged 1.5-47 years with therapy-resistant partial epilepsy (TRPE) undergoing epilepsy surgery. Control autopsy material (two temporal, two occipital, one parietal and one frontal) was removed from six neurologically healthy cases within 6-10 hours postmortem delay. In each specimen, 100-300 pyramidal and nonpyramidal neurons were visualized by intracellular Lucifer Yellow microinjection. Single neurons were imaged using CLSM generated serial optical sections; 2-D reconstruction of each neuron was made using z-projection of serial optical images, and 3-D reconstructions and rotations were computerized. Neuronal maps from TRPE biopsies, compared to control autopsies, show markedly increased numbers of dendritic abnormalities of single pyramidal and non-pyramidal neurons in layers I, II-III, V-VII, and in the subcortical white matter. The abnormalities include: (1) increased number of non-pyramidal cells in layer I; (2) many pyramidal cells with two or three dendrites originating apically, rather than one single apical dendrite, in layers II-III; (3) atypical orientation of oblique apical and basal dendrites in pyramidal neurons of layers II-VII; (4) increased number of atypical 'dinosaur-like' and fusiform cells in layers V-VII; (5) numerous neurons in the white matter. These abnormalities may be etiological in cases with early onset, and predisposing in cases with late onset.
引用
收藏
页码:233 / 247
页数:15
相关论文
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