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Tuesday, November 15, 2016'Minibrains' Could Help Drug Discovery For Zika And For Alzheimer's
This image is
from lab-grown brain tissue — a — infected by Zika
virus (white) with neural stem cells in red and neuronal nuclei in
green.
Courtesy of
Xuyu Qian and Guo-li Ming
Some tiny
clusters of brain cells grown in a lab dish are making big news at
this week's Society for Neuroscience meeting in San Diego.
Known as ","
these rudimentary networks of cells are small enough to fit on the
head of a pin, but already are providing researchers with insights
into everything from early brain development to Down syndrome,
Alzheimer's and Zika.
At a Sunday
press conference at the neuroscience meeting, researchers said are
helping them figure out how the Zika virus can disrupt human brain
formation in the early stages of fetal development.
Minibrains
are highly organized structures that actually start out as human skin
cells. They are then coaxed in the lab to become neural stem cells,
then to differentiate into some of the different types of cells found
in a real brain.
What makes
these lab-grown structures so useful is that they replicate part of
the cell diversity and connectivity of the human brain, said Dr.
Thomas Hartung, a researcher and experimental toxicologist at the
Johns Hopkins Bloomberg School of Public Health in Baltimore.
"These
cells are communicating," Hartung said. "These neurons are
talking to each other."
As a result,
the can help researchers answer questions that couldn't be
answered by studying animal brain tissue. "We need human systems
to tell us about humans, and that's why this is such a big step
forward," Hartung said.
The
first were developed a few years ago by scientists in
Europe. Since then, researchers at a handful of institutions around
the world have begun cranking out these experimental structures.
At Johns
Hopkins, Hongjun Song has been working to streamline the process and
make that are closer to the real thing in the way they
respond to viruses, for example.
When I
visited Song's lab recently, he took me to a small, windowless room
at Hopkins that has a powerful air filtration system, to show me the
result of his team's effort. He opened an incubator the size of a
dorm fridge and pointed to a device inside that was only slightly
larger than a cell phone.
The device
contains a complete factory for these organoids, he said; the system
was built by three high school interns using a 3-D printer.
The lower
half looks like a miniature muffin pan with a dozen separate
compartments. "We can grow up to 10 in each one,"
Song said.
The top half
resembles a mechanized Lego project. connected to a
dozen plastic shafts. They gently stir a precise mixture of cells,
nutrients, and growth factors in each compartment.
The that
emerge after several months in the incubator are barely big enough to
see with the naked eye, said Dr. Guo-Li Ming, a professor of
neurology at Hopkins who is married to Song and collaborates with him
on this research.
"It's
basically like a ball of cells clustering together," she said.
"But if you open it you really see something very
similar to the early embryonic brain."
Though it has
only a tiny fraction of the number of cells of an actual brain,
a grows much the way a real brain does during early
pregnancy. And that has helped researchers solve a medical mystery
involving the Zika virus.
When Zika
began making headlines last year, scientists suspected the virus
could interfere with brain development in the womb. "But you
can't study that in a mouse," Ming because mice have
very few of the developing brain cells that are most vulnerable to
Zika infection.
A student
suggested that Ming and Song use to figure out what was
happening. So the couple contacted Hengli Tang, a research biologist
they knew at Florida State University, who was studying the Zika
virus.
That call led
to studies of that showed precisely how the infection was
attacking certain neural cells, especially at a point in development
equivalent to the first trimester of pregnancy. "It was turning
[these cells] into a viral factory," Song said.
As a result,
the infected with the virus early in their development
actually decreased in size, which may help explain why a human fetus
infected with the Zika virus early in pregnancy sometimes develops
into a baby with a very small brain.
Members of
the Hopkins team are presenting details of their Zika findings this
week at the neuroscience meeting, and are already planning studies
of other disorders, including autism, schizophrenia and Alzheimer's.
Elsewhere
during the neuroscience meeting, scientists are presenting research
as a model in brain cancer and in developmental disorders, including
Down syndrome and Rett syndrome.
Minibrains'
greatest potential, though, may be for testing new drugs for brain
disorders, Hartung said. Drug testing with animals has often proved
misleading because animal brains just aren't like human brains, he
explained.
"One
company after the other failed on things like stroke, multiple
sclerosis, [and] also neurodegenerative diseases like Alzheimer's and
Parkinson's," Hartung said.
Those
failures involved drugs that worked when tested in animals, but
failed on people, Hartung said. So he has begun working with
pharmaceutical companies to see whether might offer a
better model.
One obstacle
to the widespread use of in research may be public
acceptance of the idea that scientists should be growing "brains"
in the lab. But people would be less concerned, Hartung said, if they
understood the differences between these very small, lab-grown
structures and a real brain.
For one
thing, stop growing when they still have only about 20,000
cells. A human brain has many billions. And these clumps of cells, he
explained, have no way of learning or becoming conscious.
Story
Source: The above story is based on materials provided by NATIONALPUBLICRADIO
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Materials may be edited for content and length
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