Interferon beta promotes survival in primary astrocytes through phosphatidylinositol 3-kinase

被引:43
作者
Barca, O
Ferré, S
Seoane, M
Prieto, JM
Lema, M
Señarís, R
Arce, VM [1 ]
机构
[1] Univ Santiago de Compostela, Fac Med, Dept Fisiol, Santiago De Compostela 15705, Spain
[2] Univ Santiago de Compostela, Inst Ciencias Neuroloxicas Pedro Barrie Maza, Santiago De Compostela 15705, Spain
关键词
IFN-beta; astrocytes; multiple sclerosis; apoptosis;
D O I
10.1016/S0165-5728(03)00160-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although interferon-beta (IFN-beta) has been demonstrated to be effective in the treatment of multiple sclerosis (MS) patients, the mechanism(s) underlying its beneficial effects has not been uncovered yet. Until now, most of the effort in the study of the relevant mechanisms of IFN-beta has dealt with its ability to modulate the immune response. Only recently, it has been proposed that the beneficial effects of IFN-beta in MS patients could depend on its ability to modulate astrocyte function. In the present work, we have found that IFN-beta treatment promotes the survival of astrocytes through stimulation of the phosphatidylinositol 3-kinase (PI-3K)/Akt pathway. We propose that the beneficial effects of TFN-beta in MS therapy may depend, at least in part, on its capacity to protect astrocytes against the apoptotic cell death that occurs in the early steps of the pathogenesis of MS. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:155 / 159
页数:5
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