During retinal visual processing, rod bipolar cells (RBCs) transfer scotopic signals from rods to AII amacrine cells as second-order neurons. Elucidation of the RBC excitation/inhibition is essential for understanding the visual signal transmission. Although excitation and extrinsic inhibitory mechanisms have been studied, intrinsic inhibitory mechanisms remain unclear. We focused on RBC’s prominent K + current, which exhibits voltage and Ca 2+ dependence. We isolated and confirmed intermediate-conductance Ca 2+ -activated K + channels (IK) and in RBCs using the patch-clamp method with IK inhibitors (clotrimazole and TRAM34). The regulation of the IK current primarily relies on Ca 2+ influx via low-threshold Ca 2+ channels during RBC excitation. It mediates RBC repolarization and oscillation, enabling fast and transient synaptic transmission to AII amacrine cells. Our findings highlight the unique role of the IK channel in RBC, suggesting that it plays a critical role in the scotopic pathway by fine-tuning RBC activity.
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Park et al. (2024) studied this question.
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