Key result
The schizophrenia-associated Kv11.1-3.1 isoform exhibited significantly faster deactivation (3 ms vs 8 ms at -120 mV) and slower inactivation than the Kv11.1-1A isoform, reducing current accumulation.
Absolute Event Rate: 3% vs 8%
p-value: p=<0.001
The schizophrenia-associated Kv11.1-3.1 isoform alters potassium channel gating kinetics, reducing current accumulation during repetitive depolarizations, which may contribute to disorganized neuronal firing.
Kv11.1-3.1 gating differences may influence schizophrenia-related neuronal signaling; leaves open isoform-selective therapeutic targeting.
Recent genome wide association studies identified a brain and primate specific isoform of a voltage-gated potassium channel, referred to as Kv11.1-3.1, which is significantly associated with schizophrenia. The 3.1 isoform replaces the first 102 amino acids of the most abundant isoform (referred to as Kv11.1-1A) with six unique amino acids. Here we show that the Kv11.1-3.1 isoform has faster rates of channel deactivation but a slowing of the rates of inactivation compared to the Kv11.1-1A isoform. The Kv11.1-3.1 isoform also has a significant depolarizing shift in the voltage-dependence of steady-state inactivation. The consequence of the altered gating kinetics is that there is lower current accumulation for Kv11.1-3.1 expressing cells during repetitive action potential firing compared to Kv11.1-1A expressing cells, which in turn will result in longer lasting trains of action potentials. Increased expression of Kv11.1-3.1 channels in the brain of schizophrenia patients might therefore contribute to disorganized neuronal firing.
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Heide et al. (2012) studied Schizophrenia (in vitro model). Kv11.1-3.1 isoform vs. Kv11.1-1A isoform was evaluated on Time constant of deactivation at -120 mV (p=<0.001). The schizophrenia-associated Kv11.1-3.1 isoform exhibited significantly faster deactivation (3 ms vs 8 ms at -120 mV) and slower inactivation than the Kv11.1-1A isoform, reducing current accumulation.
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