Elsevier

Brain Research

Volume 1055, Issues 1–2, 7 September 2005, Pages 196-201
Brain Research

Short Communication
A new approach to inhibiting astrocytic IP3-induced intracellular calcium increase in an astrocyte–neuron co-culture system

https://doi.org/10.1016/j.brainres.2005.06.056Get rights and content

Abstract

Astrocytes exhibit dynamic Ca2+ mobilization, such as Ca2+ wave and Ca2+ oscillation, via an inositol 1,4,5-triphosphate-induced Ca2+ release (IICR)-dependent mechanism. The physiological functions of astrocytic Ca2+ mobilization, however, are poorly understood. To investigate this issue, we created a plasmid encoding an enhanced green fluorescent protein-tagged inositol 1,4,5-triphosphate absorbent protein and expressed it in cultured astrocytes. Expression of this protein inhibited both IICR and the Ca2+ wave in cultured astrocytes. By combining this method to the single cell electroporation technique, we were able to inhibit IICR specifically in astrocytes in an astrocyte–neuron co-culture system. Our approach provides a useful tool for direct examination of the physiological role of astrocytic Ca2+ signaling on neuronal function.

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Acknowledgments

This work was supported by a WAKATE Grant-in-Aid for Scientific Research (to Sheng-Tian Li) from the Ministry of Education, Culture, Sports, Science and Technology of Japan. We thank T. Ogawa and X-J. Han for their technical assistance in culture preparation.

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