1. Cytokines are increased in the rat hippocampus after serotonergic neuron degeneration and upregulate the expression of GDH, an enzyme involved in glutamate detoxification
- Author
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E.A. Derrington, Hélène Hardin-Pouzet, Arlette Bernard, M. Didier-Bazes, Marie-Françoise Belin, and Pascale Giraudon
- Subjects
Male ,Serotonin ,Immunology ,Alpha (ethology) ,Biology ,Serotonergic ,Hippocampus ,Rats, Sprague-Dawley ,Downregulation and upregulation ,Glutamate Dehydrogenase ,Glutamates ,Transforming Growth Factor beta ,Immunology and Allergy ,Animals ,Cells, Cultured ,Tumor Necrosis Factor-alpha ,Glutamate dehydrogenase ,Glutamate receptor ,Interleukin ,Molecular biology ,Rats ,Up-Regulation ,Neurology ,Astrocytes ,Nerve Degeneration ,Tumor necrosis factor alpha ,Neurology (clinical) ,Transforming growth factor ,Interleukin-1 - Abstract
The degeneration of serotonergic neurons increases the expression of glutamate dehydrogenase (GDH) in hippocampal astrocytes. This process was demonstrated to be independent of the serotonin level. At the same time, upregulation of tumor necrosis factor (TNF) alpha and interleukin (IL)-1 alpha mRNA were observed, whereas levels of transforming growth factor (TGF) beta 1 mRNA remained unchanged. The level of GDH mRNA was increased in primary cultures of hippocampal astrocytes treated with TNF alpha and IL-1 alpha suggesting that these cytokines act on the GDH metabolism. TNF alpha and IL-1 alpha induced an increase in GDH promoter activity in C8S (an astrocytic cell line) transfected with constructs containing 5' flanking genomic sequences of GDH driving the expression of a reporter gene. These observations suggest that cytokines may be signals that upregulate the astrocytic GDH expression in response to the degeneration of serotonergic terminals in the hippocampus.
- Published
- 1996