Inflammatory cytokine levels are influenced by interactions between THP-1 monocytic, U-373 MG astrocytic, and SH-SY5Y neuronal cell lines of human origin

被引:26
作者
Klegeris, A [1 ]
McGeer, PL [1 ]
机构
[1] Univ British Columbia, Kinsmen Lab Neurol Res, Vancouver, BC V6T 1Z3, Canada
关键词
Alzheimer amyloid beta; peptide; astrocytes; brain; inflammation; interleukins; microglia; neurons; TNF-alpha;
D O I
10.1016/S0304-3940(01)02251-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We measured the secretion of interleukin (IL)1 beta, IL-6 and tumor necrosis factor-alpha (TNF-alpha )from human monocytic (THP-1), astrocytic (U-373 MG) and neuronal (SH-SY5Y) cell lines alone and in co-culture, with and without stimulation by a combination of lipopolysaccharide (LPS) plus interferon-gamma (IFN-gamma) or amyloid beta peptide 1-40 (A beta). LPS + IFN-gamma stimulation increased IL-1 beta secretion 16-fold from THP-1 cells. It increased IL-6 secretion 23-fold from THP-1 cells and 2.5-fold from U-373 MG cells. It increased TNF-alpha secretion 3.4-fold from THP-1 cells, but did not influence its secretion from U-373 MG cells. It did not affect the secretion of any of the cytokines from SH-SY5Ycells. A beta stimulation increased IL-6 secretion 2.3-fold from U-373 MG cells but did not influence secretion of IL-1 beta or TNF-alpha. A beta stimulation also failed to influence secretion of any of the cytokines from THP-1 or SH-SY5Y cells. When THP-1 and U-373 MG cells were cocultured, IL-1 beta and IL-6 secretion, but not TNF-alpha secretion, were significantly reduced from the levels obtained in independent cultures, suggesting that a mutual suppressive action may occur between microglia and astrocytes. (C) 2001 Published by Elsevier Science Ireland Ltd.
引用
收藏
页码:41 / 44
页数:4
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