Neural processes (yellow) and pre- and post-synaptic proteins (teal and magenta) in a mouse brain. Gao et al/Science 2019
In the late 19th century, the Spanish anatomist Santiago Ramón y Cajal laid the foundation for modern neuroscience with a microscope, a pen and some paper. Applying a cell-staining technique to samples of brain tissue, he produced thousands of detailed illustrations that revealed for the first time the intricate complexity of neurons and neuronal networks. Based on his observations, Ramón y Cajal proposed that the neuron was the basic functional unit of the nervous system, a fact that would not be confirmed until the 1950s with the invention of the electron microscope.
In the decades since, microscopy has remained central to efforts to understand the brain in health and disease. Scientists can today visualize brain tissues in remarkable detail, down to the level of the individual proteins responsible for neuronal structure and function.
Despite technological advances, however, challenges remain. Attempts to achieve this resolution for large samples can lead to tissue damage or can be prohibitively time-consuming—imaging an entire fruit fly brain with an electron microscope, for example, can require years or even decades of work.
Now, researchers at Howard Hughes Medical Institute’s Janelia Research Campus, MIT and Harvard Medical School have developed a method that yields high-resolution visualizations of large volumes of brain tissue, at speeds roughly 1,000 times faster than other methods.
Combining two recently developed technologies—expansion microscopy and lattice light sheet microscopy—their approach enabled them to image an entire fruit fly brain, as well as large sections of mouse cortex, in subcellular detail in only a few days.
The work—led by HHMI investigators Eric Betzig of Janelia and University of California, Berkeley and Edward Boyden of MIT, and carried out in collaboration with Blavatnik Institute at HMS—is detailed in a study published online in on Jan. 17., HMS assistant professor of pediatrics at Boston Children’s Hospital, and , HMS professor of cell biology in the
“The greatest scientific challenge of the 21st century is the brain, perhaps the most complex structure that we know of in the universe,” said Upadhyayula, who is co-first author of the study. “This new method can potentially usher in a new era for neuroscience, as we explore the ultrafine architecture of neurons and neural circuits across the brain, at scales and resolutions that were previously unattainable.”
The ability to rapidly image large volumes of brain tissue at high resolution could lead to detailed maps of the activity and wiring of the brain, the authors said, which may help scientists better understand diseases of the brain, build better artificial intelligence or even explain the molecular drivers of behavior, decision making and more.
“If we think of the brain as a city, we’ve only been able to look at small neighborhoods in detail. But now, we have the ability to create something like Google Maps,” said Kirchhausen, the HMS Springer Family Professor of Pediatrics at Boston Children’s.
“This approach could let us walk around virtually, zoom into any building or neighborhood we’re interested in, zoom out to see how they are connected and much more,” Kirchhausen said. “We can explore the city in its entirety at an exquisite level of detail, making discoveries and hopefully explaining the previously unknown.”
Study co-authors Gokul Upadhyayula, Ruixuan Gao and Tom Kirchhausen speak about the new microscope technology.
Work on the project began when co-first authors Ruixuan Gao and Shoh Asano of the Boyden lab at MIT endeavored to image complete neural circuits spanning millimeters or more using expansion microscopy. This technique, developed by Boyden and colleagues, makes small specimens larger so that molecular details can be more easily seen with conventional optical microscopes. To do so, tissue samples are infused with swellable gels—similar to what can be found in diapers. The molecules within the tissue lock into the gel scaffold, keeping the same relative positions in 3D even after expansion.
Because 3D expansion dramatically increases the volume of a sample, the team needed a microscope that was high resolution, high speed and gentle enough to not photo-bleach or otherwise damage the sample before it could be imaged in its entirety.
The solution was , developed by Betzig and colleagues, which can rapidly image tissues at subcellular resolutions. By sweeping an ultrathin sheet of light through a sample and illuminating only what lies in the microscope’s plane of focus, damage to the sample is avoided. This enables the visualization of large volumes of tissue.
“The result is that we get crystal clear images at blazingly fast speeds over very large volumes compared to earlier microscopy techniques,” Boyden said.
The team’s initial experiments combining the techniques in expanded mouse brain tissues were almost immediately successful, revealing intricate subcellular details such as dendritic spines that protrude from neurons like leaf buds on a spring tree branch.
“I couldn’t believe the quality of the data I was seeing. You could have knocked me over with a feather,” Betzig said.
Single neurons can be isolated and studied in detail. Gao et al/Science 2019
Over the past two years, the team, composed of biologists, microscopists, physicists and computer scientists, worked together to capture and analyze images of sections of mouse cortex and entire fruit fly brains.
“This is like Avengers-level collaboration,” said Gao, referring to the comic book superhero team.
The new approach is highly data intensive. To visualize the 20-million-cubic-micrometer volume of a whole fruit fly brain, for example, the team first had to image more than 51,000 3D subsections of the brain, representing roughly 10 terabytes of data. These data were then computationally stitched back together like a 3D jigsaw puzzle.
Upadhyayula led the development of bespoke algorithms to analyze the data and generate stunning movies that showcase the brain’s intricacies. Together, the team studied more than 1,500 dendritic spines, imaged fatty sheaths that insulate mouse nerve cells, highlighted all the dopaminergic neurons and mapped all the roughly 40 million synapses across the entire fly brain. The technology also provides the ability to tag and trace specific proteins through the brain, allowing new questions to be asked about structure and function.
“In our study, we barely scratched the surface in terms of the depth of information that’s buried in this incredible wealth of data,” Upadhyayula said. “We’re now working to reveal and present all of that information in a way that will let us ask questions that we couldn’t ask before because of the lack of throughput at this level of resolution.”
One of the most exciting research areas the new method enables, the authors said, is the ability to explore in molecular detail brain-to-brain differences in neurons and neuronal networks—young versus old, male versus female, healthy versus diseased.
The power of the technique can also enable visualizations and new lines of research in other organs, biological systems and a variety of diseases including cancer, the scientists said.
“Ramón y Cajal showed us the beauty and complexity of neurons, and we are essentially expanding his work to the complete volume of a brain,” Kirchhausen said. “This is important because we’re still at the stage where every time we learn something new about the brain or any other biological system, it holds consequence—whether for our understanding of ourselves, or for translational and clinical applications.
“To make serious advances, we need people who are fluent in computation and physics as much we need biologists, and it is essential that we work as a team. I think this project is an incredible demonstration of what can be achieved through exactly such teamwork.”
Dopaminergic neurons and presynaptic sites are revealed across the entire fruit fly brain. Different colors represent different brain regions. Gao et al/Science 2019
The study, “Cortical column and whole-brain imaging with molecular contrast and nanoscale resolution,” was supported by HHMI, the National Institutes of Health (1R01NS087950, 1RM1HG008525, 1R01DA045549, 2R01DA029639, 1R01NS102727, 1R41MH112318, 1R01EB024261, 1R01MH110932, R01DC015478, R44MH093011, 1DP1NS087724, R01GM075252), John Doerr, the Open Philanthropy Project, IARPA D16PC00008, U.S. Army Research Laboratory and the U. S. Army Research Office, US-Israel Binational Science Foundation, Biogen and Ionis Pharmaceuticals.
Additional authors include Igor Pisarev, Daniel E. Milkie, Tsung-Li Liu, Ved Singh, Austin Graves, Grace H. Huynh, Yongxin Zhao, John Bogovic, Jennifer Colonell, Carolyn M. Ott, Christopher Zugates, Susan Tappan, Alfredo Rodriguez, Kishore R. Mosaliganti, Shu-Hsien Sheu, H. Amalia Pasolli, Song Pang, C. Shan Xu, Sean G. Megason, Harald Hess, Jennifer Lippincott-Schwartz, Adam Hantman, Gerald M. Rubin, Stephan Saalfeld and Yoshinori Aso.
Adapted from an .