Synaptic and circuit mechanisms promoting broadband transmission of olfactory stimulus dynamics
Abstract
Sensory stimuli fluctuate on many timescales. However, short-term plasticity causes synapses to act as temporal filters, limiting the range of frequencies that they can transmit. How synapses in vivo might transmit a range of frequencies in spite of short-term plasticity is poorly understood. The first synapse in the Drosophila olfactory system exhibits short-term depression, but can transmit broadband signals. Here we describe two mechanisms that broaden the frequency characteristics of this synapse. First, two distinct excitatory postsynaptic currents transmit signals on different timescales. Second, presynaptic inhibition dynamically updates synaptic properties to promote accurate transmission of signals across a wide range of frequencies. Inhibition is transient, but grows slowly, and simulations reveal that these two features of inhibition promote broadband synaptic transmission. Dynamic inhibition is often thought to restrict the temporal patterns that a neuron responds to, but our results illustrate a different idea: inhibition can expand the bandwidth of neural coding.
Additional Information
© 2014 Macmillan Publishers Limited. Received 2 September; accepted 13 November; published online 8 December 2014; doi:10.1038/nn.3895 We thank members of the Wilson laboratory, D. Schoppik, G. Murphy and A. Liu for helpful discussions and/or comments on the manuscript. E. Yaksi performed preliminary experiments on LN temporal properties that inspired parts of this work. This work was supported by a research project grant from the US National Institutes of Health (R01 DC008174) and a Pathway to Independence Award from the US National Institutes of Health (K99 DC012065, to K.I.N.). R.I.W. receives funding from the Howard Hughes Medical Institute. Contributions: All experiments were designed by K.I.N. and R.I.W., and performed and analyzed by K.I.N., except for those shown in Figure 6c–f, which were designed by E.J.H. and R.I.W., performed by E.J.H., and analyzed by K.I.N. and E.J.H. Modeling was performed by K.I.N. K.I.N. and R.I.W. wrote the manuscript with input and critical feedback from E.J.H. The authors declare no competing financial interests.Attached Files
Supplemental Material - nn.3895-S1.pdf
Supplemental Material - nn.3895-S2.pdf
Supplemental Material - nn.3895-SF1.jpg
Supplemental Material - nn.3895-SF2.jpg
Supplemental Material - nn.3895-SF3.jpg
Supplemental Material - nn.3895-SF4.jpg
Supplemental Material - nn.3895-SF5.jpg
Supplemental Material - nn.3895-SF6.jpg
Supplemental Material - nn.3895-SF7.jpg
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Additional details
- PMCID
- PMC4289142
- Eprint ID
- 60776
- DOI
- 10.1038/nn.3895
- Resolver ID
- CaltechAUTHORS:20151005-150600571
- NIH
- R01 DC008174
- NIH
- K99 DC012065
- Howard Hughes Medical Institute (HHMI)
- Created
-
2015-10-06Created from EPrint's datestamp field
- Updated
-
2021-11-10Created from EPrint's last_modified field