Retinal Parallel Processors: More than 100 Independent Microcircuits Operate within a Single Interneuron

被引:123
作者
Grimes, William N. [1 ,2 ]
Zhang, Jun [1 ]
Graydon, Cole W. [3 ,4 ]
Kachar, Bechara [3 ]
Diamond, Jeffrey S. [1 ]
机构
[1] NINDS, Synapt Physiol Sect, NIH, Bethesda, MD 20892 USA
[2] Univ Maryland, Biophys Grad Partnership Program, NIH, Bethesda, MD 20892 USA
[3] Natl Inst Deafness & Other Commun Disorders, Sect Struct Cell Biol, NIH, Bethesda, MD 20892 USA
[4] Brown Univ, Neurosci Grad Partnership Program, NIH, Bethesda, MD 20892 USA
关键词
ROD BIPOLAR CELLS; INNER PLEXIFORM LAYER; RABBIT RETINA; MAMMALIAN RETINA; GANGLION-CELLS; AMACRINE CELLS; OLFACTORY-BULB; PYRAMIDAL NEURONS; RIBBON SYNAPSE; GRANULE CELLS;
D O I
10.1016/j.neuron.2010.02.028
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Most neurons are highly polarized cells with branched dendrites that receive and integrate synaptic inputs and extensive axons that deliver action potential output to distant targets. By contrast, amacrine cells, a diverse class of inhibitory interneurons in the inner retina, collect input and distribute output within the same neuritic network. The extent to which most amacrine cells integrate synaptic information and distribute their output is poorly understood. Here, we show that single A17 amacrine cells provide reciprocal feedback inhibition to presynaptic bipolar cells via hundreds of independent microcircuits operating in parallel. The A17 uses specialized morphological features, biophysical properties, and synaptic mechanisms to isolate feedback microcircuits and maximize its capacity to handle many independent processes. This example of a neuron employing distributed parallel processing rather than spatial integration provides insights into how unconventional neuronal morphology and physiology can maximize network function while minimizing wiring cost.
引用
收藏
页码:873 / 885
页数:13
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