A side effect of some medications is a change in the stiffness of white blood cells. The drugs tend to make the cells softer, which facilitates their entry into blood circulation.
“We are showing that white blood cells, also known as leukocytes, respond physically to these drugs and that there is a biological consequence to that response,” says Wilbur Lam, an assistant professor in the biomedical engineering department at Georgia Tech and Emory University. “This may suggest new ways to treat disease, and new places to look for diagnostic information.
“The soft cells are always flowing in the middle of the bloodstream, while the stiff ones are sequestered on the edges.”
“There may be physics-based disease biomarkers that we can use in addition to the common biological and biochemical markers we have been using.”
Lam’s research group began studying the issue to better understand a common side effect of glucocorticoid drugs such as hydrocortisone used to treat inflammatory disorders such as asthma and allergic reactions. These hormonal drugs prompt an increase in white blood cell counts, a change that had been attributed to biological processes, including a reduced “stickiness” between the cells and blood vessel walls. The increase in white cell count is also seen with drugs that support blood pressure, such as epinephrine, also known as adrenaline.
“The biological explanation for this seemed to fall short, so we thought maybe some of what was happening could be attributed to other factors–such as physical and mechanical issues,” says Lam, whose team reported findings in the Proceedings of the National Academy of Sciences.
From the edge to the center
To examine the theory, graduate student Meredith Fay and postdoctoral researcher David Myers fabricated model blood vessel systems that include artificial blood vessels with diameters as narrow as the smallest capillaries in the body. To isolate effects attributable only to physics, the systems did not include the endothelial cells that normally line blood vessels in the body.
Using blood samples taken from a healthy human volunteer, they studied the behavior of white blood cells in the presence and absence of the drugs dexamethasone–a glucocorticoid drug–and epinephrine. They also used atomic force microscopy to characterize the stiffness of individual white blood cells before and after they had been exposed to the drugs, and determined that the drugs cause the cells to become significantly softer than before exposure.
“When we fluorescently label the white blood cells and perfuse them into the artificial vessels, the white blood cells are always flowing along the edge, on the walls of these artificial blood vessels,” says Lam. “But when they are exposed to the drugs, they go to the center of the channel and enter the main blood flow. Then, we discovered that the drugs cause the cells to remodel actin, which comprises the ‘skeleton’ of all mammalian cells.”
The group’s overall hypothesis is that the body uses the mechanical properties of these cells to help control their activity and where they are located within the circulation.
The relative softness or stiffness of the cells, which collide constantly with billions of other cells in the bloodstream, including red and white blood cells, causes the cells to self-sort and determines where they end up physically within both the model blood vessels and in the human body.
“The soft cells are always flowing in the middle of the bloodstream, while the stiff ones are sequestered on the edges,” Lam says. “We believe this is how white blood cells traffic in the body and get to the site of an infection. This may be a way that the body very efficiently sorts and directs its white blood cells to get them where they’re needed.”
As a next step, Lam hopes to study how physical properties affect the movement of hematopoietic stem cells used in bone marrow transplants. Once injected intravenously into the body, the cells quickly move from the circulation to bone marrow sites where they belong, and he believes mechanical properties may also play a role in this homing process.
“Whenever there is a change in some cellular activity or physiological activity, we tend to try to explain everything at the genetic level–which genes turn off and which genes turn on,” he adds. “Gene expression is a relatively complex process, and our hypothesis is that there are probably a lot of cellular processes that are much simpler and more efficient than the typical paradigm of DNA expression, then RNA translation, and then protein production.
“A little tweak of a white blood cell’s actin will allow it to change from stiff to soft, and that small change, in and of itself, may have profound physiologic consequences and enable it to be transported from one part of the body to another.”
The team included researchers from the University of Wisconsin-Madison; Emory University; and Evergreen State College.
The National Institutes of Health, the National Science Foundation, and the American Heart Association funded the work.
Source: Georgia Tech