Thanks to an interdisciplinary team of researchers, scientists now have a more complete understanding of one of the human body's most vital structures: the red blood cell.
Led by University of Illinois electrical and computer engineering professor Gabriel Popescu, the team developed a model that could lead to breakthroughs in screening and treatment of blood-cell-morphology diseases, such as malaria and sickle-cell disease. The group published its findings in the Proceedings of the National Academy of Sciences.
Red blood cells (RBCs) are unique in structure a doughnut-shaped disc full of the oxygen-carrying molecule hemoglobin but none of the intracellular structures of other cells, not even DNA. In circulation, RBCs must contort to squeeze through capillaries half their diameter. Their flexibility and resilience come from their membrane structure, which couples a typical lipid bilayer with an underlying matrix of protein. However, knowledge of the membrane's mechanics is very limited.
"The deformability of red blood cells is their most important property," said Popescu, also affiliated with the Beckman Institute for Advanced Science and Technology at U. of I. "What we wanted to find is, how does deformability relate to morphology?"
The research team used a novel measurement technique called diffraction phase microscopy, which uses two beams of light while other microscopes only use one.
"One beam goes through the specimen and one beam is used as a reference," Popescu said. "It is very, very sensitive to minute displacements in the membrane, down to the nanoscale."
RBC membrane movement can be observed through typical light microscopes, a phenomenon known as "flickering," but Popescu's team was able not only to see nanoscale membrane fluctuations in live cells, but also to measure them quantitatively a first.
In addition to normal cells, the team also measured two other morphologies: bumpy
|Contact: Liz Ahlberg|
University of Illinois at Urbana-Champaign