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The Journal of Neuroscience, May 4, 2005, 25(18):4649-4658; doi:10.1523/JNEUROSCI.0365-05.2005

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Neurobiology of Disease
Calcineurin Triggers Reactive/Inflammatory Processes in Astrocytes and Is Upregulated in Aging and Alzheimer's Models

Christopher M. Norris,¹ Inga Kadish,² Eric M. Blalock,¹ Kuey-Chu Chen,¹ Veronique Thibault,¹ Nada M. Porter,¹ Philip W. Landfield,¹ and Susan D. Kraner¹

¹Molecular and Biomedical Pharmacology, University of Kentucky, Lexington, Kentucky 40536, and ²Cell Biology, University of Alabama, Birmingham, Alabama 35294

Astrocyte reactivity (i.e., activation) and associated neuroinflammation are increasingly thought to contribute to neurodegenerative disease. However, the mechanisms that trigger astrocyte activation are poorly understood. Here, we studied the Ca²⁺-dependent phosphatase calcineurin, which regulates inflammatory signaling pathways in immune cells, for a role in astrogliosis and brain neuroinflammation. Adenoviral transfer of activated calcineurin to primary rat hippocampal cultures resulted in pronounced thickening of astrocyte somata and processes compared with uninfected or virus control cultures, closely mimicking the activated hypertrophic phenotype. This effect was blocked by the calcineurin inhibitor cyclosporin A. Parallel microarray studies, validated by extensive statistical analyses, showed that calcineurin overexpression also induced genes and cellular pathways representing most major markers associated with astrocyte activation and recapitulated numerous changes in gene expression found previously in the hippocampus of normally aging rats or in Alzheimer's disease (AD). No genomic or morphologic evidence of apoptosis or damage to neurons was seen, indicating that the calcineurin effect was mediated by direct actions on astrocytes. Moreover, immunocytochemical studies of the hippocampus/neocortex in normal aging and AD model mice revealed intense calcineurin immunostaining that was highly selective for activated astrocytes. Together, these studies show that calcineurin overexpression is sufficient to trigger essentially the full genomic and phenotypic profiles associated with astrocyte activation and that hypertrophic astrocytes in aging and AD models exhibit dramatic upregulation of calcineurin. Thus, the data identify calcineurin upregulation in astrocytes as a novel candidate for an intracellular trigger of astrogliosis, particularly in aging and AD brain.

Key words: Ca²⁺ regulation; hypertrophy; microarray; phosphatase; reactive; glia

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Received Jan 26, 2005; revised March 31, 2005; accepted April 1, 2005.

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