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Abstract:
Retinal ganglion cells (RGCs) are the output cells of the retina; they convert synaptic input into spike output that carries visual information
to the brain. Synaptic inputs are received, integrated and communicated to the spike initiation zone of the axon by dendrites whose
properties are poorly understood. Here simultaneous patch−clamp recording and 2−photon Ca2 imaging are used to study voltage− and
light−evoked Ca2signals in the dendrites of identified types of mouse RGCs from parallelONand OFF pathways, which encode the onset
and offset of light, respectively. The results show pathway−specific differences in voltage−dependent Ca2 signaling. While both ON and
OFF cells express high−voltage−activated (HVA) Ca2channels, only OFF RGCs also express low−voltage−activated (LVA) Ca2channels.
LVA Ca2 channels in OFF cells are deinactivated by hyperpolarization from the resting potential and give rise to rebound excited Ca2
spikes at the termination of a step of either hyperpolarizing current or light. This suggests that the differential expression of voltage−gated
Ca2 channels in ON and OFF RGC dendrites contributes to differences in the way the two cell types process visual stimuli