Comparative distribution of voltage-gated sodium channel proteins in human brain

被引:119
作者
Whitaker, WRJ
Faull, RLM
Waldvogel, HJ
Plumpton, CJ
Emson, PC
Jeffrey, JJ
机构
[1] Glaxo Wellcome Res & Dev Ltd, Med Res Ctr, Dept Mol Pharmacol, Stevenage SG1 2NY, Herts, England
[2] Babraham Inst, Dept Neurobiol, Cambridge CB2 4AT, England
[3] Univ Auckland, Dept Anat, Auckland 1, New Zealand
来源
MOLECULAR BRAIN RESEARCH | 2001年 / 88卷 / 1-2期
基金
英国生物技术与生命科学研究理事会;
关键词
voltage-gated sodium channel; antibody; distribution; human brain; subcellular localization;
D O I
10.1016/S0169-328X(00)00289-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Antisera directed against unique peptide regions from each of the human brain voltage-gated sodium channel cr subunits were generated. In immunoblots these were found to be highly specific for the corresponding recombinant polypeptides and to recognise the native holoprotein in human brain membrane preparations. These antisera were used to perform a comparative immunohistochemical distribution analysis of all four brain sodium channel subtypes in selected human CNS regions. Distinct but heterogeneous distribution patterns were observed for each of the alpha subunits. In general, these were complimentary to that previously shown for the corresponding human mRNAs. A high degree of conservation with respect to the distribution found in rat was also evident. The human a subunit proteins exhibited distinct subcellular localisation patterns. Types I, m and VI immunoreactivity was predominantly in neuronal cell bodies and proximal processes, whereas type II was concentrated along axons. This is similar to rat brain and suggests the different the sodium channel subtypes have distinct functions which are highly conserved between human and rodents. A notable difference was that the type m protein was detected in all human brain regions examined, unlike in rat brain where expression in adults is very restricted. Also in contrast to rat brain, the human type VI protein was not detected in axons of unmyelinated neurons. These differences may reflect true species variation and could have important implications for understanding the function of the sodium channel subtypes and their roles in human disease. (C) 2001 Elsevier Science B;V. All rights reserved.
引用
收藏
页码:37 / 53
页数:17
相关论文
共 32 条
[1]   PRIMARY STRUCTURE, CHROMOSOMAL LOCALIZATION, AND FUNCTIONAL EXPRESSION OF A VOLTAGE-GATED SODIUM-CHANNEL FROM HUMAN BRAIN [J].
AHMED, CMI ;
WARE, DH ;
LEE, SC ;
PATTEN, CD ;
FERRERMONTIEL, AV ;
SCHINDER, AF ;
MCPHERSON, JD ;
WAGNERMCPHERSON, CB ;
WASMUTH, JJ ;
EVANS, GA ;
MONTAL, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (17) :8220-8224
[2]   DIFFERENTIAL REGULATION OF 3 SODIUM-CHANNEL MESSENGER-RNAS IN THE RAT CENTRAL NERVOUS-SYSTEM DURING DEVELOPMENT [J].
BECKH, S ;
NODA, M ;
LUBBERT, H ;
NUMA, S .
EMBO JOURNAL, 1989, 8 (12) :3611-3616
[3]   SODIUM-CHANNEL MESSENGER-RNA-I, MESSENGER-RNA-II AND MESSENGER-RNA-III IN THE CNS - CELL-SPECIFIC EXPRESSION [J].
BLACK, JA ;
YOKOYAMA, S ;
HIGASHIDA, H ;
RANSOM, BR ;
WAXMAN, SG .
MOLECULAR BRAIN RESEARCH, 1994, 22 (1-4) :275-289
[4]  
BRYSCH W, 1991, EXP BRAIN RES, V86, P562
[5]  
Burbidge S. A., 1998, Journal of Physiology (Cambridge), V513P, p130P
[6]   Sodium channel Nav1.6 is localized at nodes of Ranvier, dendrites, and synapses [J].
Caldwell, JH ;
Schaller, KL ;
Lasher, RS ;
Peles, E ;
Levinson, SR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (10) :5616-5620
[7]   From ionic currents to molecular mechanisms: The structure and function of voltage-gated sodium channels [J].
Catterall, WA .
NEURON, 2000, 26 (01) :13-25
[8]   Cloning, distribution and functional analysis of the type III sodium channel from human brain [J].
Chen, YH ;
Dale, TJ ;
Romanos, MA ;
Whitaker, WRJ ;
Xie, XM ;
Clare, JJ .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2000, 12 (12) :4281-4289
[9]   Voltage-gated sodium channels as therapeutic targets [J].
Clare, JJ ;
Tate, SN ;
Nobbs, M ;
Romanos, MA .
DRUG DISCOVERY TODAY, 2000, 5 (11) :506-520
[10]  
Dietrich PS, 1998, J NEUROCHEM, V70, P2262