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Article: Genetic deletion of SK2 channels in mouse inner hair cells prevents the developmental linearization in the Ca2+ dependence of exocytosis.

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Johnson SL; Adelman JP; Marcotti W
J. Physiol. (Lond.), 2007


Table 1. Properties of immature apical-coil IHCs from SK2 mutant mice

+/+ and +/Δ (P2–P4) Δ/Δ (P2–P4)
Steady-state activation and inactivation values (see Marcotti et al. 2003a for comparisons with normal CD-1 mice) are from fits using a first-order Boltzmann equation. Values are means ± s.e.m.; number of hair cells is in parentheses. None of the values shown above were significantly different between control and mutant IHCs.
Membrane capacitance (pF)   7.4 ± 0.2 (21)   7.3 ± 0.3 (15)
Resting potential (mV) −57.5 ± 0.8 (31) −56.5 ± 1.1 (11)
IK1 at −124 mV (pA) −112 ± 12 (10) −117 ± 20 (7) 
IK,neo at 0 mV (nA)   3.1 ± 0.1 (12)   3.1 ± 0.3 (12)
g at −84 mV (nS)   1.2 ± 0.1 (13)   1.5 ± 0.3 (8) 
IK,neo: steady-state activation
Vhalf (mV) −32.9 ± 0.7 (12) −33.5 ± 1.6 (7) 
 Slope factor, S (mV)   6.6 ± 0.2 (12)   6.6 ± 0.5 (7) 
IK,neo: steady-state inactivation
Vhalf (mV) −45.1 ± 3.3 (5)  −39.4 ± 6.6 (3) 
 Slope factor, S (mV)  16.2 ± 1.4 (5)    12.2 ± 1.5 (3)  

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Inferred neuron-electrophysiology data values

Neuron Type Neuron Description Ephys Prop Extracted Value Standardized Value Content Source
Cochlea hair cell inner cell capacitance (pF) 7.4 ± 0.2 (21) 7.4 (pF) Data Table
Cochlea hair cell inner resting membrane potential (mV) -57.5 ± 0.8 (31) -57.5 (mV) Data Table