A report on the research appears online April 22 in the journal Cell.
"We have been working for three years to develop a better research
model of brain development, and it's fortunate we can now use this one
to shed light on the major public health crisis posed by Zika
infections," says Hongjun Song, Ph.D., professor of neurology and
neuroscience at the Johns Hopkins University School of Medicine's
Institute for Cell Engineering. "This more realistic, 3-D model confirms
what we suspected based on what we saw in a two-dimensional cell
culture: that Zika causes microcephaly—abnormally small brains and
heads—mainly by attacking the neural progenitor cells that build the brain and turning them into virus factories."
Song and his wife and research partner, Guo-li Ming, M.D.,
Ph.D., professor of neurology, neuroscience, and psychiatry and
behavioral sciences, found a way to improve the bioreactors from an
unexpected source: their son and two other high school students,
from New York and Texas, who spent a summer working in the lab. The
students had worked with 3-D printers and thought they could be the key
to producing a better bioreactor, one that would fit over commonly used
12-well laboratory plates and spin the liquid and cells inside at just
the right speed to allow the cells to form brains.
Of course, it wasn't that simple, Song says. Graduate
student Xuyu Qian and postdoctoral fellow Ha Nam Nguyen, Ph.D., spent
years determining factors such as what that optimum speed was, as well
as which chemicals and growth factors should be added at what times to
yield the desired result.
The group has so far used the new bioreactor, dubbed SpinΩ,
to make three types of mini-brains mimicking the front, middle and back
of a human brain. They used the forebrain, the first mini-brain with the
six layers of brain cell types found in the human cortex, for the
current study on Zika.
"One thing the mini-brains allowed us
to do was to model the effects of Zika virus exposure during different
stages of pregnancy," says Ming. "If infection occurred very early in
development, the virus mostly infected the mini-brains' neural
progenitor cells, and the effects were very severe. After a while, the
mini-brains would stop growing and disintegrate. At a later stage,
mimicking the second trimester, Zika still preferentially infected
neural progenitor cells, but it also affected some neurons. Growth was slower, and the cortex was thinner than in noninfected brains."
These different effects correspond to what clinicians have
seen in infants born to women who contracted Zika during pregnancy, as
well as miscarriages, she notes, namely that the earlier in pregnancy
Zika infection occurs, the more severe its effects.
The research group's next step will be to test drugs already
FDA-approved for other conditions on the mini-brains to see whether one
might provide some protection against Zika. And they included 3-D
printing files for SpinΩ in the new paper so that researchers anywhere
can print their own bioreactors with just a few hundred dollars in
materials. Song says one possible future use could be to grow so-called
dopaminergic neurons for transplant, to replace those that die off in
Parkinson's disease. "This is the next frontier of stem cell biology,"
he says.
Explore further:
Evidence grows for Zika role in brain damage
More information:
Brain-Region-Specific Organoids Using Mini-bioreactors for Modeling ZIKV Exposure, Cell, www.cell.com/cell/fulltext/S0092-8674(16)30467-6 , dx.doi.org/10.1016/j.cell.2016.04.032
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