A self-defence mechanism of astrocytes against Fas-mediated death involving interleukin-8 and CXCR2

被引:33
作者
Saas, P
Walker, PR
Quiquerez, AL
Chalmers, DE
Arrighi, JF
Liénard, A
Boucraut, J
Dietrich, PY
机构
[1] Univ Hosp, Div Oncol, Lab Tumor Immunol, CH-1211 Geneva 14, Switzerland
[2] Estab Francais Sang Bourgogne Franche Comte, INSERM, E0119, UPRES EA 2284, F-25020 Besancon, France
[3] Univ Hosp, Dept Dermatol, CH-1211 Geneva 14, Switzerland
[4] Univ Hosp, Allergy Unit, CH-1211 Geneva 14, Switzerland
[5] Fac Med Marseille, Immunopathol Lab, F-13385 Marseille, France
关键词
apoptosis; astrocytes; brain; chemokine; Fas; interleukin-8;
D O I
10.1097/00001756-200210280-00018
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Astrocytes play multiple roles from passive support to the regulation of inflammation during brain injury. This latter function is in part achieved by responses induced by the triggering of Fas expressed on astrocytes both in vitro and in vivo. It was previously shown that astrocytes are resistant to Fas-mediated death, responding to Fas triggering by interleukin-8 production. However, the cellular mechanisms by which astrocytes protect themselves from Fas-mediated death are unclear. Here, we show that survival of cultured astrocytes after Fas triggering is governed by the interaction of interleukin-8 with one of its receptors, CXCR2. Furthermore, interleukin-8 secretion and CXCR2 expression are both induced in human astrocytes after Fas stimulation, suggesting a new mechanism of self-defence against Fas-mediated death.
引用
收藏
页码:1921 / 1924
页数:4
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