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. 2018 Oct 24;38(43):9186–9201. doi: 10.1523/JNEUROSCI.3572-15.2018

Table 1.

Effects of CACHD1 and α2δ-1 on biophysical properties of CaV3 subtypes

Gmax (pS/pF) V1/2 (mV) k (mV) τ Activation (ms)a τ Inactivation (ms)b
CaV3.1 (18) 628 ± 70 −34.5 ± 0.8 (30) 5.4 ± 0.1 (30) 2.0 ± 0.1 25.8 ± 2.0
CaV3.1/CACHD1 (19) 944 ± 90* −36.3 ± 0.9 (29) 5.6 ± 0.2 (29) 2.0 ± 0.2 22.2 ± 4.8
CaV3.1/α2δ-1 (13) 672 ± 90 −35.7 ± 1.4 5.6 ± 0.3 3.3 ± 0.2** 18.9 ± 0.86***
CaV3.2 (13) 596 ± 120 −34.4 ± 2.4 5.7 ± 0.2 7.1 ± 0.40 33.3 ± 0.97
CaV3.2/CACHD1 (15) 1060 ± 140**** −33.4 ± 0.8 5.9 ± 0.2 5.9 ± 0.38 32.0 ± 1.6
CaV3.3 (12) 573 ± 88 −36.1 ± 1.2 4.3 ± 0.2 24.4 ± 1.9 134 ± 12
CaV3.3/CACHD1 (10) 849 ± 78***** −38.9 ± 1.6 4.0 ± 0.3 28.5 ± 3.4 126 ± 8.3

In all cases, comparisons were performed in culture-matched experiments. Numbers in parenthesis represents the number of cells each from a minimum of five separate transfections.

aτ activation was measured at −25 mV in all cases.

bτ inactivation was measured at −20 mV for CaV3.1 and CaV3.2, and at −30 mV for CaV3.3.

*p < 0.05 vs CaV3.1 (one-way ANOVA with Bonferroni post hoc test);

**p < 0.05,

***p < 0.05, vs CaV3.1 (two-way ANOVA with Bonferroni post hoc test);

****p < 0.05 vs CaV3.2 (two-tailed unpaired Student's t test);

*****p < 0.05 vs CaV3.3 (two-tailed unpaired Student's t test).