ABOVE: A forest of dendritic spines protrudes from the branches of neurons in the mouse cortex.

A new technique that marries two methods, expansion microscopy and lattice light-sheet microscopy, has allowed researchers to image a fruit fly’s brain in its entirety with intricate detail and in a flash, relative to other microscopy approaches, scientists reported yesterday (January 17) in Science.

Expansion microscopy “blows up” the tissue before imaging to make it easier to see details. To do this, the researchers add a swelling, water-absorbent polymer gel to preserved tissue. When transferred from a salty bath to pure water, the polymer grows, stretching out the tissue. In the case of the fly brain imaged in this work, the tissue ballooned by a factor of four.

The fruit fly brain expanded to four times its usual size. 

The imaging relies on...

The method sweeps an ultrathin layer of light through the tissue. By using less intense light than other microscopes, the beam can linger on the sample while not “burning out” the fluorescence or obscuring some of the picture, Science reports.

And it’s fast, too. Because lattice light-sheet microscopy illuminates a whole plane instead of one spot, researchers were able to capture the whole fly brain in roughly 62 hours. To do this type of imaging with an electron microscope could take years, according to a press release from the Howard Hughes Medical Institute.

The imaging produces a mountain of 3D “cubes,” which need to be stitched together by computational tools. In the end, the team was able to map all 40 million plus synapses of a fruit fly brain at nanometer resolution.  

The technique yielded similar results when looking at a slice of a mouse’s brain. 

“This is a taste of the future. . . . We’re getting these huge rich data sets and we’re starting to get better tools to squeeze information from them,” Joshua Vaughan, a fluorescence microscopy expert from the University of Washington who was not involved in this work, tells STAT.


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