Induction of RANTES expression by astrocytes and astrocytoma cell lines

被引:66
作者
Barnes, DA
Huston, M
Holmes, R
Benveniste, EN
Yong, VW
Scholz, P
Perez, HD
机构
[1] UNIV ALABAMA, DEPT CELL BIOL, BIRMINGHAM, AL 35294 USA
[2] MONTREAL NEUROL INST, NEUROIMMUNOL UNIT, MONTREAL, PQ H3A 2B4, CANADA
[3] SCHERING AG, DEPT MOL & CELLULAR BIOL, BERLIN, GERMANY
关键词
astrocyte; astrocytoma; tumor necrosis factor-alpha; interleukin-1; beta; RANTES;
D O I
10.1016/S0165-5728(96)00154-3
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 cellular infiltrate found during the acute phase of multiple sclerosis (MS) consists of monocytes and activated T cells, suggesting the presence of cell-specific chemotactic signals during the inflammatory response. We examined the ability of human astrocytoma cell lines, as well as primary human and rat astrocytes, to generate a specific member of the intercrine/chemokine family of cytokines, RANTES, when exposed to TNF-alpha, IL-1 beta and IFN-gamma. Astrocytoma cells as well as primary astrocytes Produced RANTES upon incubation with TNF-alpha or IL-1 beta. IFN-gamma alone did not induce RANTES production by astrocytes, but it potentiated the effects of either TNF-alpha or IL-1 beta. Induction of RANTES by TNF-alpha was mediated by the p55 receptor since a specific anti-p55 antiserum mimicked the effect of TNF-alpha. These results indicate that human astrocytes are capable of generating a cell-specific chemokine that can account for the inflammatory cellular infiltrate observed during the acute phase of MS, in a process that is regulated by cytokines.
引用
收藏
页码:207 / 214
页数:8
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