Astrocytic IP3Rs: Contribution to Ca2+ signalling and hippocampal LTP

Astrocytes regulate hippocampal synaptic plasticity by the Ca²⁺ dependent release of the N-methyl d-aspartate receptor (NMDAR) co-agonist d-serine. Previous evidence indicated that d-serine release would be regulated by the intracellular Ca²⁺ release channel IP₃ receptor (IP₃R), however, genetic deletion of IP₃R2, the putative astrocytic IP₃R subtype, had no impact on synaptic plasticity or transmission. Although IP₃R2 is widely believed to be the only functional IP₃R in astrocytes, three IP₃R subtypes (1, 2, and 3) have been identified in vertebrates. Therefore, to better understand gliotransmission, we investigated the functionality of IP₃R and the contribution of the three IP₃R subtypes to Ca²⁺ signalling. As a proxy for gliotransmission, we found that long-term potentiation (LTP) was impaired by dialyzing astrocytes with the broad IP₃R blocker heparin, and rescued by exogenous d-serine, indicating that astrocytic IP₃Rs regulate d-serine release. To explore which IP₃R subtypes are functional in astrocytes, we used pharmacology and two-photon Ca²⁺ imaging of hippocampal slices from transgenic mice (IP₃R2^−/− and IP₃R2^−/−;3^−/−). This approach revealed that underneath IP₃R2-mediated global Ca²⁺ events are an overlooked class of IP₃R-mediated local events, occurring in astroglial processes. Notably, multiple IP₃Rs were recruited by high frequency stimulation of the Schaffer collaterals, a classical LTP induction protocol. Together, these findings show the dependence of LTP and gliotransmission on Ca²⁺ release by astrocytic IP₃Rs. GLIA 2017

Main Points

• Astrocytic IP₃Rs regulate d-serine release and LTP

• IP₃R1, IP₃R2, and IP₃R3 contribute to Ca²⁺ signalling in astrocytes

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