Table 2:

IS3 cell signature features, CIPs, measurements, and model elimination criteria

CIP stepSignature featureCharacteristic measurements of featureSelected IS3 cell measurement valuesElimination criteria (step 2)
−100 pALack of “sag”(1) Hyperpolarization Vm Difference (mean pulse value − mean initial value)−34.2649 mVNone
(2) Minimum potential time58.9000 ms
(3) Minimum potential−112.6709 mV
(4) Potential sag6.7865 mV
5) Sag time constant14.3000 ms
20 pANo spiking(1) Passive depolarization Vm difference (mean pulse value − mean initial value)12.4910 mVIf spikes are observed
50 pANormal spiking(1) Active depolarization Vm difference (mean pulse value − mean initial value)29.4174 mVIf fewer than three spikes are observed If membrane potential fails to repolarize
(2) Interspike interval36.6898 ms
(3) First spike time33.1000 ms
(4) Spike voltage threshold mean−44.3428 mV
(5) Spike half-width mean1.0301 ms
(6) Spike amplitude mean61.7296 mV
(7) Spike rate35.0044 Hz
8) Spike maximum afterhyperpolarization mean6.8820 mV
(9) Number of spikes28.0000
(10) Spike frequency adaptation1.3305
500 pADepolarization block(1) Depolarization block Vm difference (final 700 ms mean pulse value − mean initial value)62.6461 mVIf spikes in the last 700 ms of the CIP are observed If membrane potential fails to repolarize If spikes in the recovery period are observed
(2) Initial 100 ms spike rate60.0000 Hz
  • For each CIP step (1st column) we note a signature feature that is observed experimentally (2nd column), characteristic measurements that are used to quantify the signature feature (3rd column), characteristic measurement values from the selected IS3 traces (4th column), as well as conditions where models would be rejected for clearly not capturing the experimental feature (5th column). CIP, Current Injection Protocol; Vm, membrane potential.