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Holographic microscopy: Peering into living cells -- with neither dye nor fluophore

Date:
February 7, 2013
Source:
Ecole Polytechnique Fédérale de Lausanne
Summary:
Thanks to holographic microscopy, two young scientists have developed a device that can create 3-D images of living cells, almost in real time, and track their reaction to various stimuli without the use of contrast dyes or fluorophores.

Using a holographic microscope and a rotating laser beam, this image of a full living cell can be computed in minutes. The user can choose any section to see what is inside -- such as the nucleus (left) and its genetic material.
Credit: Yann Cotte - Fatih Toy - EPFL

In the world of microscopy, this advance is almost comparable to the leap from photography to live television. Two young EPFL researchers, Yann Cotte and Fatih Toy, have designed a device that combines holographic microscopy and computational image processing to observe living biological tissues at the nanoscale. Their research is being done under the supervision of Christian Depeursinge, head of the Microvision and Microdiagnostics Group in EPFL's School of Engineering.

Using their setup, three-dimensional images of living cells can be obtained in just a few minutes -- instantaneous operation is still in the works -- at an incredibly precise resolution of less than 100 nanometers, 1000 times smaller than the diameter of a human hair. And because they're able to do this without using contrast dyes or fluorescents, the experimental results don't run the risk of being distorted by the presence of foreign substances.

Being able to capture a living cell from every angle like this lays the groundwork for a whole new field of investigation. "We can observe in real time the reaction of a cell that is subjected to any kind of stimulus," explains Cotte. "This opens up all kinds of new opportunities, such as studying the effects of pharmaceutical substances at the scale of the individual cell, for example."

Watching a neuron grow

This month in Nature Photonics the researchers demonstrate the potential of their method by developing, image by image, the film of a growing neuron and the birth of a synapse, caught over the course of an hour at a rate of one image per minute. This work, which was carried out in collaboration with the Neuroenergetics and cellular dynamics laboratory in EPFL's Brain Mind Institute, directed by Pierre Magistretti, earned them an editorial in the journal. "Because we used a low-intensity laser, the influence of the light or heat on the cell is minimal," continues Cotte. "Our technique thus allows us to observe a cell while still keeping it alive for a long period of time."

As the laser scans the sample, numerous images extracted by holography are captured by a digital camera, assembled by a computer and "deconvoluted" in order to eliminate noise. To develop their algorithm, the young scientists designed and built a "calibration" system in the school's clean rooms (CMI) using a thin layer of aluminum that they pierced with 70nm-diameter "nanoholes" spaced 70nm apart.

Finally, the assembled three-dimensional image of the cell, that looks as focused as a drawing in an encyclopedia, can be virtually "sliced" to expose its internal elements, such as the nucleus, genetic material and organelles.

Toy and Cotte, who have already obtained an EPFL Innogrant, hope to develop a system that could deliver these kinds of observations in vivo, without the need for removing tissue, using portable devices. In parallel, they will continue to design laboratory material based on these principles.


Story Source:

The above story is based on materials provided by Ecole Polytechnique Fédérale de Lausanne. Note: Materials may be edited for content and length.


Journal Reference:

  1. Yann Cotte, Fatih Toy, Pascal Jourdain, Nicolas Pavillon, Daniel Boss, Pierre Magistretti, Pierre Marquet, Christian Depeursinge. Marker-free phase nanoscopy. Nature Photonics, 2013; 7 (2): 113 DOI: 10.1038/nphoton.2012.329

Cite This Page:

Ecole Polytechnique Fédérale de Lausanne. "Holographic microscopy: Peering into living cells -- with neither dye nor fluophore." ScienceDaily. ScienceDaily, 7 February 2013. <www.sciencedaily.com/releases/2013/02/130207172205.htm>.
Ecole Polytechnique Fédérale de Lausanne. (2013, February 7). Holographic microscopy: Peering into living cells -- with neither dye nor fluophore. ScienceDaily. Retrieved July 30, 2014 from www.sciencedaily.com/releases/2013/02/130207172205.htm
Ecole Polytechnique Fédérale de Lausanne. "Holographic microscopy: Peering into living cells -- with neither dye nor fluophore." ScienceDaily. www.sciencedaily.com/releases/2013/02/130207172205.htm (accessed July 30, 2014).

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