Source: Rensselaer Polytechnic Institute
Monday, March 01, 2010
New method decodes cell movements, accurately
predicts how cells will divide
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Researchers at Rensselaer Polytechnic Institute have
discovered a new method for predicting — with up to 99 percent
accuracy — the fate of stem cells.
Using advanced computer vision technology to detect subtle
cell movements that are impossible to discern with the human
eye, Professor Badri Roysam and his former student Andrew Cohen
‘89 can successfully forecast how a stem cell will split and
what key characteristics the daughter cells will exhibit.
By allowing the isolation of cells with specific
capabilities, this discovery could one day lead to effective
methods for growing stem cells on a large scale for therapeutic
use.
“If you have many cells in a culture, they all look the
same. But our new method senses all sorts of tiny differences
in the shapes and movements of the cells, and uses these cues
to predict what kind of cells it will divide into,” said Roysam, professor
of electrical, computer, and systems engineering at Rensselaer.
“We believe this method will be beneficial for one day taking
cells from a patient, and then growing large amounts of the
kind of cells that patient is in need of. This could enable
many new and exciting types of medical treatments using stem
cells.”
Results of the study, titled “Computational prediction of
neural progenitor cell fates,” were
published recently in the journal Nature
Methods.
In order to achieve successful stem cell-based therapies,
researchers require access to large amounts of specific cells.
This has proven difficult, as there are currently no methods
for controlling or manipulating the division of bulk quantities
of cells. When stem cells or progenitor cells divide via
mitosis, the resulting daughter cells can be self-renewing or
terminal. A self-renewing cell will go on to split into two
daughter cells, while a terminally differentiated cell is fated
to be a specific, specialized cell type. Researchers want the
ability to influence this division in order to produce large
volumes of the correct type of cells.
Roysam and Cohen tracked the development of rat retinal
progenitor cells cultured in their collaborator’s laboratory at
McGill University. The computer system they developed took
images of the cells every five minutes, and employed
algorithmic information theoretic prediction (AITP) to observe
the behavior of the cells, analyze the behavior, and discern
whether each individual cell is fated to split into
self-replicating or terminal daughter cells. This process
occurs in real time, so researchers know the fate of cells
before they actually divide.
The researchers predicted with 99 percent accuracy if the
rat retinal progenitor cells would split into self-renewing or
specialized cells, and predicted with 87 percent accuracy
certain characteristics of the specialized cells.
“Our results suggest that stem cells display subtle dynamic
patterns that can be sensed computationally to predict the
outcome of their next division using AITP,” Roysam said. “In
theory, AITP can be used to analyze nearly any type of cell,
and could lead to advances in many different fields.”
Roysam said prototyping and development of the system
leveraged the processing power of Rensselaer’s supercomputer,
the Computational Center
for Nanotechnology Innovations (CCNI).
Co-authors of the paper are Michel Cayouette and Francisco
Gomes of the Cellular Neurobiology Research Unit at the
Institut de Recherces Cliniques de Monteal; and Roysam’s former
student Cohen, now an assistant professor of electrical
engineering and computer science at the University of
Wisconsin, Milwaukee.
This project was supported in part by the U.S. National
Science Foundation Center for Subsurface Sensing and Imaging
Systems, the Canadian Institutes of Health Research, and the
Foundation Fighting Blindness-Canada.
For more information, visit Roysam’s Web site at: http://www.ecse.rpi.edu/~roysam.
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Published
March 1,
2010 |
Contact: Michael Mullaney
Phone: (518) 276-6161
E-mail: mullam@rpi.edu
from IMGENEX
from EMD Millipore
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