Next Generation: The Heart Camera

A new camera system allows researchers to measure multiple cardiac signals at once to understand how they interact to control heart function.

By | June 19, 2012

Calcium (top) and voltage (bottom) flux over time in rat cardiac tissue slices. Peter Lee, Christian Bollensdorff

Calcium (top) and voltage (bottom) flux over time in rat cardiac tissue slices. PETER LEE, CHRISTIAN BOLLENSDORFF

THE DEVICE: A complex interplay of signals governs the heart’s rhythm. Voltage changes and calcium flux are both important in controlling heart muscle function, with each signal influencing the other’s dynamics. Scientists at the University of Oxford have created a single camera system that can capture the dynamics of these signals simultaneously, yielding important insight into their relationship.

Peter Lee and colleagues combined several colors of light emitting diodes (LEDs) with a multi-band emission filter so that one very high speed camera could capture the different wavelengths of light emitted by various fluorescent dyes. By using different colors of LEDs, they were able to stimulate different dyes to measure changes in calcium and voltage across cardiac tissue or single layers of human cardiomyocytes (created from induced pluripotent stem cells).

WHAT’S NEW:The new setup took advantage of advances in lighting technology, explained Lee. While many older systems used xenon lamps, LEDs are cheap, cover the spectrum from infrared to ultraviolet, and reach peak intensity almost immediately—allowing for ultra-rapid switching between excitation colors. Many previous systems also relied on a moving wheel to switch between colors, and thus measure different signals, explained Guy Salama, who researches cardiac arrhythmias at the University of Pittsburgh, but was not involved in the new camera’s development. The wheels needed to move uniformly without wobbling, which would throw off its precision measurements, said Salama, and meant that each parameter had to be recorded for exactly the same amount of time. But Lee’s system, which uses electronics to control the length of time each LED shines, allows for different excitation times for each parameter of interest—which is important as not all physiological changes happen on the same time scale, said Salama. Lee’s system has also jettisoned the need for moving parts, which can require careful alignment.

Single camera and LED system.
Single camera and LED system.

IMPORTANCE: Because calcium and voltage changes interact to control cardiac function, and perturbations in either leading to dysfunctions like arrhythmia, Lee’s camera system provides researchers with a tool to further investigate the interaction between the two signals, and thus gain a deeper understanding of cardiac function.

Using a single camera with multiple emission filters also allowed Lee and his collaborators to “measure calcium properly,” Lee explained. Many previous experiments used high-affinity calcium dyes, which bound strongly but could perturb the signal. The strong LEDs allowed for weaker-binding dyes, and “ratiometric” calcium measurement, meaning the dyes display shifts in emission wavelength upon binding calcium. Researchers can then quantify the concentration of calcium based on the light emissions they detect and calcium flux simultaneously.

Additionally, explained Lee, the simplicity of the system makes it more easily scalable. LEDs are cheap and perform well, and the lack of moving parts makes setup much easier than multi-camera systems that need careful calibration.

NEEDS IMPROVEMENT: As appealingly simple as a one-camera setup is, a single camera and multiple light sources can also introduce new hurdles, explained Salama. Because one camera is being used to capture multiple parameters, this cuts down on the number of image frames that can be devoted to each signal, noted Salama. For example, if a camera is running at 1,000 frames per second, but imaging four signals, only 250 of those frames would capture each parameter.

Salama also feared that lining up the LEDs and camera might result in the different light sources hitting the cardiac tissue at different angles, and bouncing off at different angles, making it difficult for the camera to capture them all. When visualizing the voltage and calcium propagations over a single layer of cells, scientists need to make sure the emissions they’re comparing are coming from the same location—so they aren’t trying to match voltage changes in one set of cells with calcium fluxes in another. When imaging microscopic-scale changes, Lee works around this problem by merging the lights into one path and using an optical fiber to direct all the colors to one site.

So far, the new camera setup only images one sample at a time, but Lee is working to build a high-throughput system, envisioning its use as a screening tool that could help visualize how drugs affect signal propagation in an array of myocyte layers or cardiac tissue. He is also designing custom emission-band filters, so researchers can visualize more parameters with different dyes, like pH or mitochondrial potential. “Where we’re headed is expansion,” Lee said.

P. Lee et al., “Simultaneous voltage and calcium mapping of genetically purified human induced pluripotent stem cell-derived cardiac myocyte monolayers,” Circulation Research, doi:10.1161/CIRCRESAHA.111.262535, 2012.



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