Finally some exciting pathology news, as if there is such a thing. Scientists at the Spectroscopy Laboratory at MIT developed a novel technique to create 3D images of live organelles, cells, and even small organisms. The idea is to recreate a volumetric image from multiple 2D ones, all of which were obtained from different angles, and were based on refractive index patterns:
“You can reconstruct a 3D representation of an object from multiple images taken from multiple directions,” said Wonshik Choi, lead author of the paper and a Spectroscopy Laboratory postdoctoral associate.
Cells don’t absorb much visible light, so the researchers instead created their images by taking advantage of a property known as refractive index. Every material has a well-defined refractive index, which is a measure of how much the speed of light is reduced as it passes through the material. The higher the index, the slower the light travels.
The researchers made their measurements using a technique known as interferometry, in which a light wave passing through a cell is compared with a reference wave that doesn’t pass through it. A 2D image containing information about refractive index is thus obtained.
To create a 3D image, the researchers combined 100 two-dimensional images taken from different angles. The resulting images are essentially 3D maps of the refractive index of the cell’s organelles. The entire process took about 10 seconds, but the researchers recently reduced this time to 0.1 seconds.
The team’s image of a cervical cancer cell reveals the cell nucleus, the nucleolus and a number of smaller organelles in the cytoplasm. The researchers are currently in the process of better characterizing these organelles by combining the technique with fluorescence microscopy and other techniques.
“One key advantage of the new technique is that it can be used to study live cells without any preparation,” said Kamran Badizadegan, principal research scientist in the Spectroscopy Laboratory and assistant professor of pathology at Harvard Medical School, and one of the authors of the paper. With essentially all other 3D imaging techniques, the samples must be fixed with chemicals, frozen, stained with dyes, metallized or otherwise processed to provide detailed structural information.
“When you fix the cells, you can’t look at their movements, and when you add external contrast agents you can never be sure that you haven’t somehow interfered with normal cellular function,” said Badizadegan.
The current resolution of the new technique is about 500 nanometers, or billionths of a meter, but the team is working on improving the resolution. “We are confident that we can attain 150 nanometers, and perhaps higher resolution is possible,” Feld said. “We expect this new technique to serve as a complement to electron microscopy, which has a resolution of approximately 10 nanometers.”
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