Pro-inflammatory cytokines induce the transcription factors C/EBPβ and C/EBPδ in astrocytes

Authors

  • Jean-René Cardinaux,

    1. Institut de Physiologie et Laboratoire de Recherche du Service de Neurologie du CHUV, Faculté de Médecine, Université de Lausanne, Lausanne, Switzerland
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  • Igor Allaman,

    1. Institut de Physiologie et Laboratoire de Recherche du Service de Neurologie du CHUV, Faculté de Médecine, Université de Lausanne, Lausanne, Switzerland
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  • Pierre J. Magistretti

    Corresponding author
    1. Institut de Physiologie et Laboratoire de Recherche du Service de Neurologie du CHUV, Faculté de Médecine, Université de Lausanne, Lausanne, Switzerland
    • Institut de Physiologie, Université de Lausanne, 7 rue du Bugnon, CH-1005 Lausanne, Switzerland.
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Abstract

The transcription factors CCAAT/enhancer binding protein (C/EBP)-β and -δ are key regulators for the expression of the acute phase genes in the liver, such as complement component C3 and antichymotrypsin. In the brain, these acute phase proteins are produced in response to pro-inflammatory cytokines by the reactive astrocytes, in particular those surrounding the amyloid plaques of Alzheimer's disease brains. Here we show that lipopolysaccharides (LPS), IL-1β, and TNFα induce the expression of the c/ebpβ and genes in mouse primary astrocytes. This induction precedes the expression of the acute phase genes coding for the complement component C3 and the mouse homologue of antichymotrypsin. The induction of these two acute phase genes by LPS is blocked by cycloheximide, whereas this protein synthesis inhibitor does not affect the expression of the c/ebp genes. Altogether, our data support a role as immediate-early genes for c/ebpβ and , whose expression is induced by pro-inflammatory cytokines in mouse cortical astrocytes. In the liver, these transcription factors are known to play an important role in inflammation and energy metabolism regulation. Therefore, C/EBPβ and -δ could be pivotal transcription factors involved in brain inflammation, in addition to their previously demonstrated role in brain glycogen metabolism regulation (Cardinaux and Magistretti. J Neurosci 16:919–929, 1996). GLIA 29:91–97, 2000. © 2000 Wiley-Liss, Inc.

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