Feedback network controls photoreceptor output at the layer of first visual synapses in Drosophila
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Date
2006
Authors
L Zheng
GG Polavieja
V Wolfram
MH Asyali
RC Hardie
M Juusola
Journal Title
Journal ISSN
Volume Title
Publisher
ROCKEFELLER UNIV PRESS
Open Access Color
Green Open Access
Yes
OpenAIRE Downloads
OpenAIRE Views
Publicly Funded
No
Abstract
At the layer of first visual synapses information from photoreceptors is processed and transmitted towards the brain. In fly compound eye output from photoreceptors (R1 - R6) that share the same visual field is pooled and transmitted via histaminergic synapses to two classes of interneuron large monopolar cells (LMCs) and amacrine cells (ACs). The interneurons also feed back to photoreceptor terminals via numerous ligand-gated synapses yet the significance of these connections has remained a mystery. We investigated the role of feedback synapses by comparing intracellular responses of photoreceptors and LMCs in wild-type Drosophila and in synaptic mutants to light and current pulses and to naturalistic light stimuli. The recordings were further subjected to rigorous statistical and information-theoretical analysis. We show that the feedback synapses form a negative feedback loop that controls the speed and amplitude of photoreceptor responses and hence the quality of the transmitted signals. These results highlight the benefits of feedback synapses for neural information processing and suggest that similar coding strategies could be used in other nervous systems.
Description
Keywords
EXTERNAL PLEXIFORM LAYER, INFORMATION-TRANSFER, LIGHT ADAPTATION, WILD-TYPE, SHIBIRE, FLY, TRANSMISSION, MELANOGASTER, POTENTIALS, SYSTEM, Patch-Clamp Techniques, Light, Temperature, Articles, Models, Biological, Synaptic Transmission, Feedback, Electrophysiology, Drosophila melanogaster, Interneurons, Animals, Evoked Potentials, Visual, Photoreceptor Cells, Invertebrate, Microelectrodes, Signal Transduction
Fields of Science
0301 basic medicine, 0303 health sciences, 03 medical and health sciences
Citation
WoS Q
Scopus Q

OpenCitations Citation Count
93
Source
The Journal of General Physiology
Volume
127
Issue
Start Page
495
End Page
510
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Citations
CrossRef : 84
Scopus : 82
PubMed : 53
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Mendeley Readers : 92
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