Time- and activation-dependency of the protective effect of microglia on astrocytes exposed to peroxide-induced oxidative stress

被引:5
作者
Armbrust, E. [1 ]
Roehl, C. [1 ,2 ]
机构
[1] Univ Kiel, Dept Anat, D-24098 Kiel, Germany
[2] Univ Kiel, Inst Toxicol & Pharmacol Nat Scientists, D-24105 Kiel, Germany
关键词
glial cell interactions; gliosis; hydrogen peroxide; oxidative stress; microglia; astrocyte; co-culture;
D O I
10.1016/j.tiv.2008.02.008
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 [卫生毒理学];
摘要
Microglial as well as astroglial activation (gliosis) are common phenomena of neuropathological processes in the brain. Nevertheless, the role of glial cell communication during gliosis is still not completely understood. The data We present with this work are a part of a bigger study on microglial-astroglial cell communication. The purpose of this study was to examine the impact of microglial-astroglial cell interactions on the cytotoxic effect of hydrogen peroxide (H2O2) on astrocytes and to characterize the microglia-induced astroprotective effect in detail. Therefore, purified cell cultures of microglia and astroglia from neonatal rat brains were used. Astrocytes were pretreated with conditioned medium from lipopolysaccharides (LPS)-activated microglia and then exposed to oxidative stress induced by H2O2 under varying conditions. Activated microglia significantly reduced the cytotoxic effect of H2O2. As well in the indirect co-culture model using conditioned medium of microglia as in a direct co-culture model with different portions of microglial cells on the astroglial monolayer the astroprotective effect clearly correlated with the degree of microglial activation. The protective effect on astrocytes was induced in less than 24 h and lasted more than 4 days. Taken together, our results indicate that microglial activation might play an important role in the modulation of the oxidative stress resistance of glial tissue during gliosis. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1399 / 1404
页数:6
相关论文
共 21 条
[1]
Microglia and inflammation-mediated neurodegeneration: Multiple triggers with a common mechanism [J].
Block, ML ;
Hong, JS .
PROGRESS IN NEUROBIOLOGY, 2005, 76 (02) :77-98
[2]
Desagher S, 1996, J NEUROSCI, V16, P2553
[3]
Astrocyte-enhanced neuronal survival is mediated by scavenging of extracellular reactive oxygen species [J].
Drukarch, B ;
Schepens, E ;
Stoof, JC ;
Langeveld, CH ;
Van Muiswinkel, FL .
FREE RADICAL BIOLOGY AND MEDICINE, 1998, 25 (02) :217-220
[4]
GFAP AND ASTROGLIOSIS [J].
ENG, LF ;
GHIRNIKAR, RS .
BRAIN PATHOLOGY, 1994, 4 (03) :229-237
[5]
Microglial reaction induced by noncytotoxic methylmercury treatment leads to neuroprotection via interactions with astrocytes and IL-6 release [J].
Eskes, C ;
Honegger, P ;
Juillerat-Jeanneret, L ;
Monnet-Tschudi, F .
GLIA, 2002, 37 (01) :43-52
[6]
Factors influencing nominal effective concentrations of chemical compounds in vitro:: cell concentration [J].
Gülden, M ;
Mörchel, S ;
Seibert, H .
TOXICOLOGY IN VITRO, 2001, 15 (03) :233-243
[7]
Diverse microglial responses after intrahippocampal administration of lipopolysaccharide [J].
Herber, DL ;
Maloney, JL ;
Roth, LM ;
Freeman, MJ ;
Morgan, D ;
Gordon, MN .
GLIA, 2006, 53 (04) :382-391
[8]
The acute and the long-term effects of nigral lipopolysaccharide administration on dopaminergic dysfunction and glial cell activation [J].
Iravani, MM ;
Leung, CCM ;
Sadeghian, M ;
Haddon, CO ;
Rose, S ;
Jenner, P .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2005, 22 (02) :317-330
[9]
Pro-regenerative properties of cytokine-activated astrocytes [J].
Liberto, CM ;
Albrecht, PJ ;
Herx, LM ;
Yong, VW ;
Levison, SW .
JOURNAL OF NEUROCHEMISTRY, 2004, 89 (05) :1092-1100
[10]
Role of microglia in inflammation-mediated neurodegenerative diseases: Mechanisms and strategies for therapeutic intervention [J].
Liu, B ;
Hong, JS .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2003, 304 (01) :1-7