Extracellular Calcium Controls Background Current and Neuronal Excitability via an UNC79-UNC80-NALCN Cation Channel Complex

Summary

In contrast to its extensively studied intracellular roles, the molecular mechanisms by which extracellular Ca²⁺ regulates the basal excitability of neurons are unclear. One mechanism is believed to be through Ca²⁺'s interaction with the negative charges on the cell membrane (the charge screening effect). Here we show that, in cultured hippocampal neurons, lowering [Ca²⁺]_e activates a NALCN channel-dependent Na⁺-leak current (I_L-Na). The coupling between [Ca²⁺]_e and NALCN requires a Ca²⁺-sensing G protein-coupled receptor, an activation of G-proteins, an UNC80 protein that bridges NALCN to a large novel protein UNC79 in the same complex, and the last amino acid of NALCN's intracellular tail. In neurons from nalcn and unc79 knockout mice, I_L-Na is insensitive to changes in [Ca²⁺]_e, and reducing [Ca²⁺]_e fails to elicit the excitatory effects seen in the wild-type. Therefore, extracellular Ca²⁺ influences neuronal excitability through the UNC79-UNC80-NALCN complex in a G protein-dependent fashion.