Astrocytic IP₃ Rs: 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 (IP₃ R), however, genetic deletion of IP₃ R2, the putative astrocytic IP₃ R subtype, had no impact on synaptic plasticity or transmission. Although IP₃ R2 is widely believed to be the only functional IP₃ R in astrocytes, three IP₃ R subtypes (1, 2, and 3) have been identified in vertebrates. Therefore, to better understand gliotransmission, we investigated the functionality of IP₃ R and the contribution of the three IP₃ R subtypes to Ca²⁺ signalling. As a proxy for gliotransmission, we found that long-term potentiation (LTP) was impaired by dialyzing astrocytes with the broad IP₃ R blocker heparin, and rescued by exogenous d-serine, indicating that astrocytic IP₃ Rs regulate d-serine release. To explore which IP₃ R subtypes are functional in astrocytes, we used pharmacology and two-photon Ca²⁺ imaging of hippocampal slices from transgenic mice (IP₃ R2^-/- and IP₃ R2^-/- ;3^-/- ). This approach revealed that underneath IP₃ R2-mediated global Ca²⁺ events are an overlooked class of IP₃ R-mediated local events, occurring in astroglial processes. Notably, multiple IP₃ Rs 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 IP₃ Rs. GLIA 2017;65:502-513.