Neuregulin: An oligodendrocyte growth factor absent in active multiple sclerosis lesions

被引:60
作者
Viehover, A
Miller, RH
Park, SK
Fischbach, G
Vartanian, T
机构
[1] Beth Israel Deaconess Med Ctr, Dept Neurol, Boston, MA 02215 USA
[2] Harvard Med Sch, Boston, MA USA
[3] Case Western Reserve Univ, Dept Neurosci, Cleveland, OH 44106 USA
[4] Columbia Univ, Coll Phys & Surg, Off Dean, New York, NY USA
关键词
development; differentiation; erbB; glial growth factor; heregulin; myelination; neuregulin; oligodendrocyte; regeneration; remyelination;
D O I
10.1159/000048721
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Multiple sclerosis (MS) is an inflammatory demyelinating disease of the central nervous system (CNS) which results in demyelination and axonal injury. Conventional therapy for MS is immune suppression in the absence of agents that promote neural and glial survival or remyelination. Neuregulins are a family of ligands that exert trophic effects on both neurons and glia. Using mice bearing a null mutation in the neuregulin gene, here we demonstrate that neuregulins are necessary for the normal development of oligodendrocytes. In addition, neuregulins are produced in the normal human CNS by astrocytes as well as neurons. Astrocyte-derived neuregulin is functionally active in bioassays and exists in secreted and membrane-associated beta-isoforms. In active and chronic active MS lesions, however, the expression of astrocyte neuregulin is dramatically reduced. The absence of neuregulin in active MS lesions may contribute to the paucity of remyelination in MS. Copyright (C) 2001 S. Karger AG, Basel.
引用
收藏
页码:377 / 386
页数:10
相关论文
共 80 条
[1]   The N-terminal domain of the myelin oligodendrocyte glycoprotein (MOG) induces acute demyelinating experimental autoimmune encephalomyelitis in the Lewis rat [J].
Adelmann, M ;
Wood, J ;
Benzel, I ;
Fiori, P ;
Lassmann, H ;
Matthieu, JM ;
Gardinier, MV ;
Dornmair, K .
JOURNAL OF NEUROIMMUNOLOGY, 1995, 63 (01) :17-27
[2]   PURIFICATION AND PARTIAL STRUCTURAL AND FUNCTIONAL-CHARACTERIZATION OF MOUSE MYELIN OLIGODENDROCYTE GLYCOPROTEIN [J].
AMIGUET, P ;
GARDINIER, MV ;
ZANETTA, JP ;
MATTHIEU, JM .
JOURNAL OF NEUROCHEMISTRY, 1992, 58 (05) :1676-1682
[3]   OLIGODENDROCYTE LYSIS BY CD4(+) T-CELLS INDEPENDENT OF TUMOR-NECROSIS-FACTOR [J].
ANTEL, JP ;
WILLIAMS, K ;
BLAIN, M ;
MCREA, E ;
MCLAURIN, JA .
ANNALS OF NEUROLOGY, 1994, 35 (03) :341-348
[4]  
Baerwald KD, 1998, J NEUROSCI RES, V52, P230, DOI 10.1002/(SICI)1097-4547(19980415)52:2<230::AID-JNR11>3.3.CO
[5]  
2-P
[6]   CELL-DEATH AND CONTROL OF CELL-SURVIVAL IN THE OLIGODENDROCYTE LINEAGE [J].
BARRES, BA ;
HART, IK ;
COLES, HSR ;
BURNE, JF ;
VOYYODIC, JT ;
RICHARDSON, WD ;
RAFF, MC .
CELL, 1992, 70 (01) :31-46
[7]  
BEN BN, 1994, P SOC EXP BIOL MED, V206, P221
[8]  
BerminghamMcDonogh O, 1996, DEVELOPMENT, V122, P1427
[9]   REACTIVE NITROGEN INTERMEDIATES IN HUMAN NEUROPATHOLOGY - AN OVERVIEW [J].
BROSNAN, CF ;
BATTISTINI, L ;
RAINE, CS ;
DICKSON, DW ;
CASADEVALL, A ;
LEE, SC .
DEVELOPMENTAL NEUROSCIENCE, 1994, 16 (3-4) :152-161
[10]   The neuregulin, glial growth factor 2, diminishes autoimmune demyelination and enhances remyelination in a chronic relapsing model for multiple sclerosis [J].
Cannella, B ;
Hoban, CJ ;
Gao, YL ;
Garcia-Arenas, R ;
Lawson, D ;
Marchionni, M ;
Gwynne, D ;
Raine, CS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (17) :10100-10105