The inflammatory transcriptome of reactive murine astrocytes and implications for their innate immune function

被引:87
作者
Falsig, J
Pörzgen, P
Lund, S
Schrattenholz, A
Leist, M
机构
[1] Univ Zurich, Inst Neuropathol, CH-8032 Zurich, Switzerland
[2] H Lundbeck & Co AS, Valby, Denmark
[3] ProteoSys AG, Mainz, Germany
关键词
chemokines; gene regulation; inflammation; neuroimmunology; proteomics;
D O I
10.1111/j.1471-4159.2005.03622.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Upon injury, astrocytes assume an activated state associated with the release of inflammatory mediators. To model this, we stimulated murine primary astrocytes with a complete inflammatory cytokine mix consisting of TNF-alpha, IL-1 beta and IFN-gamma. We analysed the transcriptional response of 480 genes at 4 and 16 h after stimulation on a chip designed to give a representative overview over the inflammation-relevant part of the transcriptome of macrophage-like cells. The list of the 182 genes found to be significantly regulated in astrocytes revealed an intriguing co-ordinate regulation of genes linked to the biological processes of antiviral/antimicrobial defence, antigen presentation and facilitation of leucocyte invasion. The latter group was characterized by very high up-regulations of chemokine genes. We also identified regulations of a thymidylate kinase and an interferon-regulated protein with a tetratricopeptide motive, both up to now only known from macrophages. The transcriptional regulations were confirmed on the protein level by a proteomic analysis. These findings taken together suggest that activated astrocytes in brain behave similarly in many respects to inflamed macrophages in the periphery.
引用
收藏
页码:893 / 907
页数:15
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