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Microscopy decodes complex eye circuitry

May 2011
Compiled by BioPhotonics staff

Minute neural eye cell structures can now be viewed in tissue at high resolution, and researchers say the technique could bring clarity to the study of circuit patterns in all regions of the nervous system.

A combination of two microscopy methods allowed researchers at the Max Planck Institute to discover that the synapses between retinal ganglion cells and starburst amacrine cells are distributed asymmetrically. When viewed from the ganglion cell, the starburst cell dendrites connected with it run opposite to the preferred direction of motion. Their work appeared in the March 10, 2011, issue of Nature (doi: 10.1038/nature09818).

Cells and synapses reconstructed from serial block face electron microscopy data. The image depicts a single starburst amacrine cell (yellow) and two direction-selective ganglion cells (green). Although there is substantial dendritic overlap with both cells, all connections (magenta) go to the correct ganglion cell. Courtesy of Kevin Briggman, Max-Planck-Gesellschaft.

The scientists made the discovery by combining a new electron microscopy method known as serial block face electron microscopy with two-photon fluorescence microscopy. First, with the latter, they determined the preferred motion direction of the ganglion cells. A calcium-sensitive fluorescent dye indicated the stimulation of calcium flow into the cell – a process that signals electrical activity within the cells.

The optic signals in the outer segments of the photoreceptor cells are transduced into electrical signals. Excitatory and inhibitory synapses convey these signals to the ganglion cell. Courtesy of

Then, using serial block face electron microscopy, they measured the exact trajectory of all of the ganglion cell’s dendrites, as well as those connected to amacrine cells. The new process used an electron beam to produce a volumetric image by repeatedly scanning the surface of a tissue sample. Using an extremely sharp diamond knife, they “sliced” the sample surface after each scan.

Tracing the fine, densely packed branched dendrites of retinal neurons, the scientists clearly identified their synapses. The complete automation of the imaging process enabled them to record data sets with up to tens of thousands of sections.

amacrine cellsBiophotonicsBioScancell structurescircuit patternsdendriteselectron beamelectron microscopyEuropefluorescent dyeganglion cellGermanyMax-Planck-GesellschaftmicroscopesMicroscopymicroscopy two-photon fluorescence microscopeNewsopticsretinal ganglion cellsserial block face electron microscopystarburst amacrine cellsstarburst cell dendritesWinfried Denk

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