Say hello to the stunning results of CLARITY — a new technique that enables scientists to turn brain matter and other tissues completely transparent. It’s already being hailed as one of the most important advances for neuroanatomy in decades, and it’s not hard to see why.
Cut off a mouse’s head. Carefully remove its brain, wash it gently, and you’ll wind up with something resembling the sample pictured above, on the left. Grey matter, it so happens, lives up to its name. Due in large part to molecules known as lipids, organs like the brain are usually opaque. Lipids comprise cell membranes and provide structural support to a variety of organs and tissues throughout the body – but they also scatter light. As a result, most microscopes are lucky if they can peer even a millimeter into biological matter before images in the viewfinder get blurry.
One of the more popular techniques scientists use to get around this hangup is called “sectioning.” It’s brutally straightforward in practice: a researcher will freeze a chunk of tissue (a mouse brain, for example) in liquid nitrogen, and then slice it into scores of little sheets, each one just a fraction of a millimeter thick. This turns a single 3-dimensional problem (otherwise inscrutable, due to its non-transparent nature) into a series of 2-dimensional ones. Go through a brain layer by layer, and you can cobble together a volumetric picture of everything from cellular structure, to the spatial distribution of proteins, to the various connections that form between neurons. But the tradeoff is substantial. You’re literally cutting your sample into a bunch of tiny little pieces. With every slice, tissue is deformed, connections are severed, information is lost.
CLARITY does away with the slicing and dicing entirely. The technique, described in the latest issue of Nature by a team led by Stanford researchers Kwanghun Chung and Karl Deisseroth, works by stripping away all of a tissue’s light-scattering lipids, while leaving everything else right where it belongs. You’ll recall, however, that lipids play an important structural role in organs like the brain; if you remove them, everything else falls apart — a fact that has plagued past attempts at making tissues see-through. But that’s where CLARITY is different.
CLARITY works by virtue of a bait and switch. In their study, Chung and Deisseroth submerge a mouse brain in a mixture of formaldehyde and acrylamide. The former attaches important cellular structures and components to the latter, which solidifies into a gel when heated. An electrical current is then coursed through the gel, stripping it of anything not hanging on. The lipids go bye-bye, and the brain goes clear as Jell-O. More importantly: all of its significant structures remain intact and in place. Neurons, synapses, proteins, DNA. Every last component is exactly where it should be.
The ability to strip a brain of its lipids and nothing else gives rise to remarkable research possibilities. In the image above, a mouse brain turned transparent with CLARITY has been made visible again by labeling specific neurons with a fluorescent marker that glows green. Researchers have been using this technique (called “immunolabeling”) to highlight certain molecular and structural features for years, but with CLARITY, labeled cells can be seen in three dimensions, all at once.
In fact, the process of removing the brain’s lipids actually makes the tissues more permeable, making it easier to not only tag them with fluorescent markers in the first place, but untagthem and then tag them again with an entirely different label. What’s more, the fact that you don’t have to cut a brain up to see how it was stained means that you can add more tags to the same brain. The picture below shows a region of the brain known as the hippocampus that has had its different neurons labeled in a variety of fluorescent colors. A brain that was once impermeable to light has been made invisible, only to be made visible again – but this time with remarkable specificity.
There’s nothing that says this technique couldn’t be used on human brains, so long as you have the time. Coloring-in a clarified brain like the one above requires soaking it in solution with the fluorescent labels you want to tag it with. For a mouse brain, that can take a month or more. For a brain as voluminous as a human’s, it would take much longer. (While Chung and Deisseroth did demonstrate their technique could be used on human brains, they did so with a small block of tissue, not an entire brain.)
Likewise, there’s nothing that says CLARITY could not be used on tissues besides the brain, though the organ certainly shows the most immediate promise. The ability to visualize the neuronal connections throughout a transparent brain, for example, could spur incredible growth in the field of connectomics, which seeks to map the brain’s neuronal wiring. In neuroscience, few tools are as coveted as those that enable you to see the part and the whole simultaneously – CLARITY could enable researchers to study the structure and distribution of individual neurons in the context of the whole brain. “This is the kind of innovation that will slingshot neuroscience far beyond today,” said Henry Markram, leader of Europe’s recently unveiled Human Brain Project, in an interview with NatGeo’s Ed Yong. “This new method of whole-brain imaging across all levels of the brain provides a way to acquire much of the key data we will need.”