Macrophages: their myelinotrophic or neurotoxic actions depend upon tissue oxidative stress

被引:16
作者
Bartnik, BL
Juurlink, BHJ
Devon, RM
机构
[1] Univ Saskatchewan, Dept Oral Biol, Saskatoon, SK S7N 5E5, Canada
[2] Univ Saskatchewan, Cameco Multiple Sclerosis & Neurosci Res Ctr, Saskatoon, SK S7N 5E5, Canada
[3] Univ Saskatchewan, Dept Anat & Cell Biol, Saskatoon, SK S7N 5E5, Canada
来源
MULTIPLE SCLEROSIS | 2000年 / 6卷 / 01期
关键词
cell culture; demyelinating disease; inflammation; myelin; multiple sclerosis; oligodendroglia;
D O I
10.1177/135245850000600108
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
There are still questions regarding whether macrophages found in MS lesions ore agents of recovery or of destruction. To address this, we examined in aggregate cultures prepared from dissociated embryonic spinal cord tissue, with or without addition of exogenous macrophages, the effect of menadione-induced oxidative stress. Similar to findings of other laboratories, we observed that in the absence of oxidative stress macrophage enrichment Promoted myelinogenesis. In macrophage-poor cultures, menadione at 5 mu M had very little effect upon the status of the aggregate cultures; however, increasing this to 10 and 20 mu M did result in some damage to axons and myelin. By contrast in macrophage enriched cultures, menadione at a concentration as little as 5 mu M caused the complete destruction of the aggregates We suggest that in neural tissues that have sufficiently high macrophage numbers, oxidative stress results in a positive inflammatory feedback loop that results in massive tissue destruction. We further suggest that what we see in macrophage-enriched aggregates subjected to oxidative stress may represent what happens in the Marburg-type of MS lesion.
引用
收藏
页码:37 / 42
页数:6
相关论文
共 43 条
[1]   The NF-kappa B and I kappa B proteins: New discoveries and insights [J].
Baldwin, AS .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :649-683
[2]  
Brandwene Elliott L., 1996, Journal of Emergency Medicine, V14, P691, DOI 10.1016/S0736-4679(96)00177-1
[3]   CYTOKINE LOCALIZATION IN MULTIPLE-SCLEROSIS LESIONS - CORRELATION WITH ADHESION MOLECULE EXPRESSION AND REACTIVE NITROGEN SPECIES [J].
BROSNAN, CF ;
CANNELLA, B ;
BATTISTINI, L ;
RAINE, CS .
NEUROLOGY, 1995, 45 (06) :S16-S21
[4]   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
[5]   MONOCYTE-MACROPHAGE DIFFERENTIATION IN EARLY MULTIPLE-SCLEROSIS LESIONS [J].
BRUCK, W ;
PORADA, P ;
POSER, S ;
RIECKMANN, P ;
HANEFELD, F ;
KRETZSCHMAR, HA ;
LASSMANN, H .
ANNALS OF NEUROLOGY, 1995, 38 (05) :788-796
[6]   THE ADHESION MOLECULE AND CYTOKINE PROFILE OF MULTIPLE-SCLEROSIS LESIONS [J].
CANNELLA, B ;
RAINE, CS .
ANNALS OF NEUROLOGY, 1995, 37 (04) :424-435
[7]   Macrophage microglial-mediated primary demyelination and motor disease induced by the central nervous system production of interleukin-3 in transgenic mice [J].
Chiang, CS ;
Powell, HC ;
Gold, LH ;
Samimi, A ;
Campbell, IL .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (06) :1512-1524
[8]   3 MODELS OF FREE RADICAL-INDUCED CELL INJURY [J].
COMPORTI, M .
CHEMICO-BIOLOGICAL INTERACTIONS, 1989, 72 (1-2) :1-56
[9]  
Conrad R.E., 1981, MANUAL MACROPHAGES M
[10]  
CUZNER ML, 1994, NEUROPATH APPL NEURO, V20, P200