Modulation of Fas-Ligand (Fas-L) on human microglial cells: an in vitro study

被引:22
|
作者
Frigerio, S
Silei, V
Ciusani, E
Massa, G
Lauro, GM
Salmaggi, A
机构
[1] Ist Nazl Neurol C Besta, I-20133 Milan, Italy
[2] Univ Studi Roma Tre, I-00146 Rome, Italy
关键词
microglia; Fas-Ligand; apoptosis;
D O I
10.1016/S0165-5728(99)00227-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The expression of Fas-ligand (Fas-L) on microglia could be relevant in multiple sclerosis immunopathology. The present study was performed to evaluate in vitro the expression of Fas-L in human microglial cells both unstimulated and after stimulation with IFN-gamma, beta-IFN-1b and beta-IFN-1b+IFN-gamma. Cells were stimulated for 6,12,24 and 48 h. Surface Fas-L was evaluated by flow cytometry, total Fas-L by Western blot, whereas mRNA for Fas-L was measured by RT-PCR. We also evaluated the capacity of microglial cells to induce, in vitro, apoptosis on Fas-positive T leukemia Jurkat cells. Our results showed a constitutive expression of Fas-L on microglia. IFN-gamma downregulated the expression of the molecule, while beta-IFN-1b and beta-IFN-1b+IFN-gamma did not. The amount of surface Fas-L was related to the ability of microglial cells to induce apoptosis in Fas-positive target cells, which was partly inhibited by blockade of the Fas-Fas-L pathway. (C) 2000 published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:109 / 114
页数:6
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