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Calcium/calcineurin signaling in primary cortical astrocyte cultures: Rcan1‐4 and cyclooxygenase‐2 as NFAT target genes
Author(s) -
Canellada Andrea,
Ramirez Belén G.,
Minami Takashi,
Redondo Juan Miguel,
Cano Eva
Publication year - 2008
Publication title -
glia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.954
H-Index - 164
eISSN - 1098-1136
pISSN - 0894-1491
DOI - 10.1002/glia.20647
Subject(s) - calcineurin , nfat , biology , calcium , microbiology and biotechnology , astrocyte , calcium in biology , calcium signaling , signal transduction , endocrinology , medicine , transplantation , intracellular , central nervous system
Abstract The calcineurin/nuclear factor of activated T cells (NFAT) signaling pathway mediates important cell responses to calcium, but its activity and function in astrocytes have remained unclear. We show that primary cortical astrocyte cultures express the regulatory and catalytic subunits of the phosphatase calcineurin as well as the calcium‐regulated NFAT family members (NFATc1, c2, c3, and c4). NFATs are activated by calcium‐mobilizing agents in astrocytes, and this activation is blocked by the calcineurin inhibitor cyclosporine A. Microarray screening identified cyclooxygenase‐2 ( Cox‐2 ), which is implicated in brain injury, and Rcan 1‐4 , an endogenous calcineurin inhibitor, as genes up‐regulated by calcineurin‐dependent calcium signals in astrocytes. Mobilization of intracellular calcium with ionophore potently augments the promoter activity and mRNA and protein expression of Rcan 1‐4 and Cox‐2 induced by combined treatment with phorbol esters. Moreover, Rcan 1‐4 expression is efficiently induced by calcium mobilization alone. For both the genes, the calcium signal component is dependent on calcineurin and is replicated by exogenous expression of a constitutively active NFAT, strongly suggesting that the calcium‐induced gene activation is mediated by NFATs. Finally, we report that calcineurin‐dependent expression of Cox‐2 and Rcan 1‐4 is induced by physiological calcium mobilizing agents, such as thrombin, agonists of purinergic and glutamate receptors, and L‐type voltage‐gated calcium channels. These findings provide insights into calcium‐initiated gene transcription in astrocytes, and have implications for the regulation of calcium responses in astrocytes. © 2008 Wiley‐Liss, Inc.