Clogging
of pipes leading to the heart is the planet's number one killer. Surgeons can
act as medical plumbers to repair some blockages, but we don't fully understand
how this living organ deteriorates or repairs itself over time.
Researchers at the University of Washington have
studied vessel walls and found the cells pull more tightly together, reducing
vascular leakage, in areas of fast-flowing blood. The finding could influence
how doctors design drugs to treat high cholesterol, or how cardiac surgeons
plan their procedures.
Their paper will be published in an upcoming issue
of the American Journal of Physiology -- Heart and Circulatory Physiology.
"Our results indicate that these cells can
sense the kind of flow that they're in, and structurally change how they hold
themselves together," said lead author Nathan Sniadecki, a UW assistant
professor of mechanical engineering. "This highlights the role that
cellular forces play in the progression of cardiovascular disease."
It's known that the arteries carrying blood are
leakier in areas of slow flow, promoting cholesterol buildup in those areas.
But medical researchers believed this leakage was mostly biochemical -- that
cells would sense the slower flow and modify how proteins and enzymes function
inside the cell to allow for more exchange.
The new results show that, like a group of
schoolchildren huddling closer in a gust of wind, the cells also pull more
tightly together when the blood is flowing past.
"The mechanical tugging force leads to a
biochemical change that allows more and more proteins at the membrane to glue
together," Sniadecki said. "We're still trying to understand what's
happening here, and how mechanical tugging leads more proteins to localize and
glue at the interface."
Sniadecki's group looks at the biomechanics of
individual cells. For this experiment, they grew a patch of human endothelial
cells, the thin layer of cells that line the inner walls of arteries and veins
and act as a sort of nonstick coating for the vessels' walls. They grew the
patch on an area about the width of a human hair, manufactured with 25 by 25
tiny flexible silicon posts.
The researchers then looked at how much the cells
bent the posts under different flow conditions in order to calculate how
strongly the cells were tugging on their neighbors. When the flow was fast, the
force between the cells increased, while the gaps between cells shrank.
Knowing how cells respond to blood flow could help
find new drugs to promote this tugging between cells. Better understanding of
the interaction between blood flow and heart health could also guide surgeries.
"People could do simulations so a surgeon goes,
'Ah, I should cut here versus over here, because that reconstruction will be a
smoother vessel and will lead to fewer complications down the line, or as I put
this stent in, put it here and make it more aerodynamic in design,'"
Sniadecki said.
Co-authors are Lucas Ting, Joon Jung, Benjamin
Shuman, Shirin Feghhi, Sangyoon Han, Marita Rodriguez in the UW's department of
mechanical engineering, and Jessica Jahn at UW Medicine.
The research was funded by the National Institutes
of Health, the National Science Foundation, the UW Medical Student Research
Training Program and the UW Royalty Research Fund.
ScienceDaily
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