Intracellular microlasers emit narrowband fluorescence to precisely label a trillion cells

Inducing structures incorporated within individual cells produce laser light, allowing precise labeling of individual cells.

Content Dam Bow Online Articles 2015 July 96427 Web

Massachusetts General Hospital (MGH; Boston, MA) researchers have induced structures incorporated within individual cells to produce laser light. The wavelengths of light emitted by the intracellular microlasers differ based on factors such as the size, shape, and composition of each microlaser, allowing precise labeling of individual cells.

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Current fluorescent dyes used for research and medical diagnosis are limited because they emit a very broad spectrum of light, so only a handful of dyes can be used at once since their spectral signatures would overlap, according to Seok Hyun Yun, Ph.D., of the Wellman Center for Photomedicine at MGH, who is the corresponding author of the report. But the narrowband spectrum of light emitted by the research team's intracellular lasers enable labeling of up to a trillion cells individually, adds lead author Matjaž Humar, Ph.D., also of the Wellman Center. What's more, the very specific wavelengths emitted by the microlasers also allow measurements of small changes happening within a cell with much greater sensitivity than is possible with broadband fluorescence.

Previous studies by Yun's lab demonstrated the first laser based on a living cell, which used fluorescent proteins as the gain medium to amplify the light signal. But this first-generation cellular laser required a laser cavity consisting of a pair of mirrors placed outside the cell to generate laser light. For the current study, Yun and Humar used tiny spherical objects capable of confining light by reflection from their inner surfaces as microcavities for the amplification of laser light within the cavity.

The first versions used droplets of oil—either injected into individual cells or naturally occurring within the fat cells called adipocytes—and showed that either could be induced to emit specific wavelengths of laser light by pumping energy from an external laser into fluorescent dyes diffused into the droplet, a process that produced minimal heating of the cells. Changes in the shape of the droplet induced by miniscule pressure alterations within the cell altered the spectra of light emitted, and those alterations could be readily measured. Along with showing lasing with a variety of cells—such as cancer cells, fibroblasts, macrophages, and adipocytes extracted from the skin of pigs—the researchers also induced adipocytes residing within a piece of porcine skin to emit clearly visible laser light.

Content Dam Bow Online Articles 2015 July 96427 Web
Massachusetts General Hospital investigators have induced subcutaneous fat cells in a piece of skin from a pig to emit laser light in response to energy delivered through an optical fiber. (Credit: Matjaž Humar, Ph.D., and Seok Hyun Yun, Ph.D., Wellman Center for Photomedicine, Massachusetts General Hospital)

Production of laser light within solid plastic fluorescent microbeads, which are readily taken up into cells, resulted in unique signature spectra based on the size and number of beads within a cell and the fluorescent dye used. The investigators calculated that it would be possible to tag individual cells with more than a trillion different laser signatures, a number that matches the estimated number of cells in the human body.

Yun, also an associate professor of dermatology at Harvard Medical School, says that a next step for the research team will be figuring out how to use biologically generated energy from mechanical movement or a biochemical reaction to pump a cellular laser in a living body. They envision lasers completely made out of materials that are safe for use within the human body, which could enable remote sensing within the body or be used in laser-light therapies, he says.

Full details of the work appear in the journal Nature Photonics; for more information, please visit http://dx.doi.org/10.1038/nphoton.2015.129.

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