Expression and localization of voltage dependent potassium channel Kv4.2 in epilepsy associated focal lesions

被引:32
作者
Aronica, E. [1 ,2 ]
Boer, K. [1 ]
Doorn, K. J. [1 ]
Zurolo, E. [1 ]
Spliet, W. G. M. [3 ]
van Rijen, P. C. [4 ]
Baayen, J. C. [5 ]
Gorter, J. A. [2 ,6 ]
Jeromin, A. [7 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Neuropathol, NL-1105 AZ Amsterdam, Netherlands
[2] Epilepsy Inst Netherlands SEIN, Heemstede, Netherlands
[3] Univ Med Ctr Utrecht, Dept Pathol, Utrecht, Netherlands
[4] Univ Med Ctr Utrecht, Dept Neurosurg, Rudolf Magnus Inst Neurosci, Utrecht, Netherlands
[5] Free Univ Amsterdam, Dept Neurosurg, Med Ctr, Amsterdam, Netherlands
[6] Univ Amsterdam, Swammerdam Inst Life Sci, Ctr Neurosci, NL-1105 AZ Amsterdam, Netherlands
[7] Allen Inst Brain Sci, Seattle, WA USA
关键词
Hippocampal sclerosis; Focal cortical dysplasia; Cortical tubers; Ganglioglioma; Immunocytochemistry; Epilepsy; NEURONAL CALCIUM SENSOR-1; ACTIVATED PROTEIN-KINASE; GENE-EXPRESSION; K+ CURRENTS; CLINICOPATHOLOGICAL CLASSIFICATION; CORTICAL DYSPLASIA; KV CHANNELS; RAT-BRAIN; MALFORMATIONS; MODEL;
D O I
10.1016/j.nbd.2009.06.016
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
An increasing number of observations suggest an important role for voltage-gated potassium (Kv) channels in epilepsy. We studied the cell-specific distribution of Kv4.2, phosphorylated (p) Kv4.2 and the Kv4.2 interacting protein NCS-1 using immunocytochemistry in different epilepsy-associated focal lesions. In hippocampal sclerosis (HS), Kv4.2 and pKv4.2 immunoreactivity (IR) was reduced in the neuropil in regions with prominent neuronal cell loss. In both HS and malformations of cortical development (MCD), intense labeling was found in neuronal somata, but not in dendrites. Strong NCS-1 IR was observed in neurons in all lesion types. Western blot analysis demonstrated an increase of total Kv4.2 in all lesions and activation of the ERK pathway in HS and ganglioglioma. These findings indicate that Kv4.2 is expressed in both neuronal and glial cells and its regulation may involve potassium channel interacting proteins, alterations in the subcellular localization of the channel, as well as phosphorylation-mediated posttranslational modifications. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:81 / 95
页数:15
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