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ANN
ARBOR, Mich.---Picture a honeycomb and each compartment
in the honeycomb is coated with living cells from
a person's mouth, skin or a piece of bone.
University of Michigan associate professor Nicholas
Kotov believes that one day, the cells in those honeycombs
can be used to grow spare parts for our bodies, or
even an entire artificial immune system in a bottle.
An immune system in a bottle
would allow faster and easier production of a flu
vaccine, thus preventing another shortage, he said.
In addition, the immune system in a bottle will give
scientists clues how to design vaccines that activate
an immune response to the unchanging part of a flu
virus, making yearly vaccinations, quite possibly,
unnecessary, Kotov said.
In the paper "Inverted
Colloidal Crystals as 3-D Cell Scaffolds," published
last month in the journal Langmuir, Kotov's lab in
the chemical engineering department and other collaborators
introduced a way to build those cell-incubating honeycombs---called
scaffolds---so that even though the cells occupy different
compartments in the honeycomb, they share the same
conditions, just as they would share the same conditions
if growing in the body.
Collaborators on the paper
include researchers from Oklahoma State University,
University of Texas Medial Branch and Stillwater Oklahoma-based
Nomadics Inc. Kotov has appointments in the biomedical,
materials science and chemical engineering departments.
The research is so important
that the Defense Advanced Research Projects Agency
(DARPA) has funded a consortium of research institutions
for $10 million to grow the immune system in a bottle.
Scientists can study the artificial
immune system to see how it reacts to biological hazards
and their countermeasures, and use the data to make
more effective countermeasures, said Jan Walker, DARPA
spokesman.
The birthplace of this artificial
immune system is Kotov's three dimensional scaffold,
which is comprised of inverted colloidal crystals,
also called photonic crystals. Colloidal crystals
are hexagonally ordered lattices of highly uniform
spherical particles that are packed together. They
have a wide range of diameters, from nanometers to
micrometers and this versatility is critical for controlling
the life cycle of cells and how they change (i.e.
differentiation).
Kotov's team didn't use robotics
or complicated computer set-ups to make the scaffolds.
Instead, they used heat and gel to make a simple mold.
First, they infiltrated the
crystal with sol gel. When the gel hardened in the
channels between the spheres, scientists heated the
crystal to burn away all but the walls left by the
hardened gel. What's left is an inverted replica,
or a mold, of the crystal.
Historically, scientists cultured
cells in plates or dishes where they grow in two-dimensional
colonies. But because cells proliferate three dimensionally
in the body, it's critical that scientists develop
a three-dimensional scaffold for cell cultures so
the cells' development can mimic what happens inside
us. This is particularly important for differentiation
of stem cells into different lineages of immune cells.
The inverted colloidal crystal scaffold could stimulate
differentiation of human stem cells from blood of
adults to functional T and B cells. T and B cells
help target and kill foreign invaders.
"The uniformity of the
environment affects the way the cells are developing,"
Kotov said. "This is particularly relevant for
stem cells and other cells that can differentiate.
These scaffolds offer a very good control over the
environment."
The final goal of the DARPA
project will be replication of the function of the
human bone marrow and thymus. Besides University of
Texas Medical Branch and Nomadics Inc., it also includes
Harvard University, Massachusetts General Hospital,
Scientific Research Laboratory Inc, and Fred Hutchinson
Cancer Center. Later, the artificial bone marrow and
thymus will be integrated with other elements of the
human immune system being developed in the multiuniversity
team lead by VaxDesign Inc. The ability of the inverted
colloidal crystal scaffolds to control the differentiation
process of the cells also opens possibilities in using
for treatment of leukemia and other forms of cancer.
For information on Kotov: http://www.engin.umich.edu/dept/cheme/people/kotov.html
The Kotov research group: http://www.engin.umich.edu/dept/che/research/kotov/
The Defense Advanced Research
Projects Agency: http://www.darpa.mil/
The University of Michigan
College of Engineering is ranked among the top engineering
schools in the country. Michigan Engineering boasts
one of the largest research budgets of any public
university, at $139 million for 2003. Michigan Engineering
has 11 departments and two NSF Engineering Research
Centers. Within those departments and centers, there
is a special emphasis on research in three emerging
industries: Nanotechnology and integrated microsystems;
cellular and molecular biotechnology; and information
technology. The College is seeking to raise $110 million
for capital building projects and program support
in these areas to further research discovery. The
CoE's goal is to advance academic scholarship and
market cutting edge research to improve public heath
and well-being. For more information see the CoE home
page: http://www.engin.umich.edu/index.html
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