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. Author manuscript; available in PMC: 2011 Nov 4.
Published in final edited form as: Neuron. 2010 Nov 4;68(3):488–499. doi: 10.1016/j.neuron.2010.09.014

Figure 2. Control of Resting Na+ Leak Current by Extracellular Ca2+ in Cultured Hippocampal Neurons.

Figure 2

(A) Representative holding currents at –68 mV in a wild-type (+/+) neuron. Na+-leak current is presented as ΔIL-Na (indicated by the double arrow), defined as the difference between holding currents in 140 mM (solid bar) and 14 mM (open bar) Na+-containing baths. A 0.25 sec recording is shown for each condition. ΔIL-Na increased when [Ca2+]e was switched from 2 mM (indicated by the hatched bar labeled 2 Ca) to 0.1 mM (0.1 Ca). (B) ΔIL-Na in wild-type neurons measured at various [Ca2+]e normalized to that measured with 2 mM [Ca2+]e (n ≥ 5). (C) Similar to (A), but from a NALCN-/- neuron. (D) Comparison of ΔIL-Na between wild-type (+/+) and NALCN-/- neurons at a range of [Ca2+]e, as indicated. The number of cells for each condition is indicated in parentheses. (E) Representative ΔIL-Na restored by NALCN cDNA transfection into the NALCN-/- neurons. (F) Summary of ΔIL-Na generated by NALCN or mock (empty vector) transfection in 2 mM and 0.1 mM [Ca2+]e (mean ± SEM). See also Figure S2.