Light can control waves in heart tissue - Jadugai Students Corner

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Friday 4 December 2015

Light can control waves in heart tissue

heart

Researchers have found a new way to take charge of an out-of-control heart. All it takes is a light touch — literally touching the heart with a pulse of visible light.
Your heart beats tens of thousands of times each day. Its pace may speed up or slow down as your activities change. Yet its rate remains fairly regular, thanks to electrical signals that travel as waves from cell to cell through the heart. Those waves spread in somewhat the same way that a wave ripples through a baseball stadium as fans stand up and sit down in a coordinated fashion.
But watch out if something goes wrong with the heart’s waves of activity.
A wave sometimes spirals back on itself, for example. It’s almost looks “like a dog chasing its own tail,” explains Gil Bub. As a biophysicist at the University of Oxford in England, he studies the physics of life functions, particularly those of the heart. Such spiral waves that cross back on themselves can make the heart beat too quickly. And that can be deadly.
Medicines or electrical devices can reset — or sometimes even take over — someone’s heartbeat. However, such approaches basically jolt the whole heart. Now, however, there’s a new method to fine tune the control of waves in that muscle that makes up your heart.
“What we’ve done is figure out a way to use light to control waves in a way that hadn’t been done before,” explains Bub. To do that, his group at Oxford worked with biomedical engineer Emilia Entcheva and her colleagues at Stony Brook University in New York.
Together, the researchers used a fairly new technology called optogenetics Opto- refers to light. Genetics deals with the biological instructions in our cells. The technology uses light to either turn on or shut down genetically programmed actions in cells.
Until now, most people working in this field focused on the brain and nervous system. Among them is Keith Bonin, a physicist at Wake Forest University in Winston-Salem, N.C. He has used optogenetics to study brain cells called neurons. Electrical signals travel through these nerve cells and cause the release of chemicals that send messages to neighboring neurons.
Muscle cells in the heart also produce electrical signals. However, these signals spread from cell to cell in a different way — as waves. Working with heart-muscle cells, Bonin says, “is an interesting new application of the tools of optogenetics.”
 How the technique works

The left image shows how waves in heart tissue can swirl back to cause problems with the heartbeat. Using light, researchers have stopped that unhealthy swirling (right image).
Burton et al. Nature Photonics 2015
In the lab, Bub’s group grew normal cells from the heart muscle of a rat. Those cells would naturally grow together to form heart tissue. But the scientists added something — a virus developed at Entcheva’s lab. She and her group had engineered that virus to change the heart cells’ genes. That change now allows blue light to open gate-like channels in the cells’ outer walls, or membranes.Those channels let in charged atoms, called ions. These ions, mostly of sodium plus some calcium, have a positive charge, so they’re also called cations (KAT-eye-uns). When enough of them flow in, an electric current begins to flow. If the current becomes strong enough, it triggers processes in the cell. Those processes lead to an electrical spike, called an action potential. The cell responds by contracting.  
The action potential also sets off a wave of activity that spreads to other cells. Those cells in turn go through processes that lead to electrical activity and cause each cell to contract. The wave of activity is what allows the heart to contract in a coordinated way.
Using a computer-controlled projector, researchers shone blue light through a cable made of optical fibers onto a few heart cells. This started the flow of ions. And very precise changes in the aim and strength of the light could affect the electrical waves.
“We can control the direction” of the waves, says Bub. “We can control how fast they go.” The technique even can change the swirling of a spiral wave, also known as its chirality (Ky-RAAL-ih-tee). In heart tissue, a wave can swirl clockwise or counterclockwise, in a left-handed or right-handed direction. And if blue light shines on all the affected cells, it can shut down existing waves altogether.
In the future
Optogenetics “gives us a great way of doing experiments we couldn’t do before,” says Bub. “It gives us a really cool way of controlling how the waves propagate so we can understand the general patterns that are made.”
The technique also lets researchers compare waves moving through heart tissue against waves in other tissues or groups of cells. For example, similar waves can be seen in slime-mold colonies, the eye’s retina and the brain. Travelling waves also happen in physical systems (such as winds) and in some chemical reactions.
At some point in the next few decades, optogenetics might even lead to new ways to treat heart disease. Doctors generally do not treat disease by altering genes in people or changing how they work. Work along those lines is called gene therapy. It focuses mainly on diseases that are currently incurable.
However, gene therapy could become common in the future. If that happens, then perhaps doctors could make damaged parts of patients’ hearts sensitive to light. Afterward, doctors could use optogenetics to regulate a patient’s heartbeat.
Eventually, the approach might prove safer and less painful than other treatments, such as electrical shocks or surgery to implant pacemakers (which eventually wear out). But, Bub adds, that’s a long way off.
Bonin agrees that many questions need to be resolved. For one, can the new method control the muscles’ motion in the same way that the heart usually does? “Being able to reproduce actual mechanical motion that can mimic real tissue would be an important future step,” Bonin says.
Other issues include learning how to modify heart muscle cells in a living patient. To do that, biomedical engineers first would have to figure out how and when to deliver light to those cells in a precise way. There are lots of other medical, practical and ethical hurdles, too, notes Bub.

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