Microglia activation influences dye coupling and Cx43 expression of the astrocytic network

被引:80
作者
Faustmann, PM [1 ]
Haase, CG [1 ]
Romberg, S [1 ]
Hinkerohe, D [1 ]
Szlachta, D [1 ]
Smikalla, D [1 ]
Krause, D [1 ]
Dermietzel, R [1 ]
机构
[1] Ruhr Univ Bochum, Dept Neuroanat & Mol Brain Res, D-44780 Bochum, Germany
关键词
astrocytes; microglia; gap junction; connexin; 43; inflammation;
D O I
10.1002/glia.10141
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Under inflammatory conditions, activated microglia are capable of producing proinflammatory cytokines that are reported to influence cell-to-cell communication. The present study was performed to evaluate the influence of microglial activation on the coupling efficiency of the astroglial network. Primary astrocyte cultures of newborn rats were cocultured with either 5% (M5) or 30% (M30) microglia. Microglial activation (rounded phagocytotic phenotype) was investigated using the monoclonal anti-ED1 antibody, and immunofluorescence with a polyclonal anti-Cx43 antibody was used to study astroglial. Cx43 expression and distribution. Functional coupling of astrocytes was evaluated by monitoring the transfer of microinjected Lucifer yellow into neighboring cells. The data obtained can be summarized as follows: astroglia/M30 cocultures contained significantly fewer resting microglia and significantly more activated microglia than the M5 cocultures; significantly reduced astroglial Cx43 staining was found in M30 cocultures concurrently with a reduced number of dye coupled astrocytes; and the positive correlation of percent activated microglia with reduced astroglial Cx43 expression was highly significant, indicating that the degree of intercellular communication in the astroglial network may be modulated by the activation of microglia under in vitro conditions.
引用
收藏
页码:101 / 108
页数:8
相关论文
共 57 条
[1]   CYTOTOXICITY OF MICROGLIA [J].
BANATI, RB ;
GEHRMANN, J ;
SCHUBERT, P ;
KREUTZBERG, GW .
GLIA, 1993, 7 (01) :111-118
[2]   EVIDENCE FOR MOTILITY AND PINOCYTOSIS IN RAMIFIED MICROGLIA IN TISSUE-CULTURE [J].
BOOTH, PL ;
THOMAS, WE .
BRAIN RESEARCH, 1991, 548 (1-2) :163-171
[3]  
BROSNAN CF, 2001, AM J PATHOL, V158, P1775
[4]   COGNITIVE IMPAIRMENT IN PATIENTS WITH CLINICALLY ISOLATED LESIONS OF THE TYPE SEEN IN MULTIPLE-SCLEROSIS - A PSYCHOMETRIC AND MRI STUDY [J].
CALLANAN, MM ;
LOGSDAIL, SJ ;
RON, MA ;
WARRINGTON, EK .
BRAIN, 1989, 112 :361-374
[5]   Membrane currents and morphological properties of neurons and glial cells in the spinal cord and filum terminale of the frog [J].
Chvátal, A ;
Anderová, M ;
Ziak, D ;
Orkand, RK ;
Syková, E .
NEUROSCIENCE RESEARCH, 2001, 40 (01) :23-35
[6]  
Dermietzel R, 1998, GLIA, V24, P1, DOI 10.1002/(SICI)1098-1136(199809)24:1<1::AID-GLIA1>3.0.CO
[7]  
2-A
[8]  
DERMIETZEL R, 1991, J NEUROSCI, V11, P1421
[9]  
Dermietzel R., 2000, ADV MOL CEL, V30, P323
[10]  
DIJKSTRA CD, 1985, IMMUNOLOGY, V54, P589