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

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Abstract

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-α, IL-1β and IFN-γ. 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. © 2005 International Society for Neurochemistry.

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Falsig, J., Pörzgen, P., Lund, S., Schrattenholz, A., & Leist, M. (2006). The inflammatory transcriptome of reactive murine astrocytes and implications for their innate immune function. Journal of Neurochemistry, 96(3), 893–907. https://doi.org/10.1111/j.1471-4159.2005.03622.x

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