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Characterisation of bipolar cell synaptic transmission in goldfish retina using paired recordings
Author(s) -
Palmer Mary J.
Publication year - 2010
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2009.185850
Subject(s) - neuroscience , ribbon synapse , excitatory postsynaptic potential , kainate receptor , postsynaptic current , ampa receptor , postsynaptic potential , neurotransmission , cnqx , inhibitory postsynaptic potential , exocytosis , chemistry , glutamate receptor , biology , biophysics , synaptic vesicle , receptor , endocrinology , biochemistry , vesicle , membrane , secretion
Direct recordings from the large axon terminals of goldfish retinal bipolar cells (BCs) have revealed detailed information about the properties and regulation of exocytosis at this ribbon‐type synapse. However, the relationship between BC exocytosis and evoked postsynaptic responses in amacrine and ganglion cells is not known. To address this, I have made paired recordings from BC terminals (BCTs) and neurons in the ganglion cell layer (GCL) in goldfish retinal slices. BCT depolarisation evoked short‐latency, AMPA/kainate receptor‐mediated EPSCs in connected GCL neurons. NMDA receptors contributed to the response at +40 mV but not at −60 mV. Evoked EPSCs contained multiple temporal components that differed in their relative amplitudes between pairs. Changing the duration or amplitude of the presynaptic stimulus affected the size and kinetics of the EPSC, with weaker stimuli slowing the EPSC activation rate. Paired‐pulse stimulation caused greater depression of fast than slow EPSC components. A linear relationship was found between the amount of BCT exocytosis, measured via changes in membrane capacitance, and the charge of evoked EPSCs, whether they were mediated by AMPA/kainate receptors alone or in combination with NMDA receptors. In addition, analysis of miniature EPSCs in GCL neurons provided estimates of the quantal content of evoked EPSCs. The results demonstrate the feasibility of using this paired recording system to study synaptic transfer at ribbon synapses, and indicate that both the rapid and sustained phases of BC exocytosis are encoded in the postsynaptic response.