The unitary event amplitude of mouse retinal on-cone bipolar cells

被引:16
作者
Berntson, A [1 ]
Taylor, WR
机构
[1] Australian Natl Univ, John Curtin Sch Med Res, Div Neurosci, Canberra, ACT, Australia
[2] Australian Natl Univ, Ctr Visual Sci, Canberra, ACT, Australia
关键词
mouse; retina; bipolar cells; light responses; noise analysis; whole-cell voltage clamp;
D O I
10.1017/S0952523803206040
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Light-evoked synaptic currents were recorded from on-cone bipolar cells in the mouse retina. Fluctuations in the synaptic current observed during maintained light steps were analyzed in order to estimate the amplitude of the underlying unitary event. The maximal synaptic current variance was 5-fold larger than the maximum expected from fluctuations in the number of active postsynaptic channels. Due to uncertainty in the contribution from channel variance, we calculated a range of values for the unitary event amplitude. The observed variance could be accounted for if 30-39 synaptic sites randomly generated unitary events with a waveform identical to the flash-response, and an amplitude of -3.1 to -2.4 pA. The amplitude is consistent with gating about five mGluR6 channels. The shape of the variance-mean relation suggests that in bright light transmitter release approaches zero, while in darkness transmitter release saturates the postsynaptic response. Thus the on-cone bipolar cell synapse is operating over its entire possible range. If it is assumed that the postsynaptic response saturates when one unitary event occurs per integration time, then a lower bound for the unitary event rate is 18 events/s/synaptic site. If the unitary event is generated by a single synaptic vesicle, the results suggest the total vesicle cycling rate available for encoding the on-cone bipolar cell signal is about 540-700 s(-1).
引用
收藏
页码:621 / 626
页数:6
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