Essential
features of the cortex, an important part of the human brain and its
development, are more accurately captured in organoids generated by researchers
of the Princess Máxima Center for pediatric oncology and the Hubrecht
Institute. The scientists developed mini-organs with features like cell
organization, stem cell expansion and cell identity that more closely mimic the
real-life situation. These novel organoids can be used as a basis to model
pediatric brain tumors.
Multiple childhood brain tumors,
like cortical gliomas, arise from the cortex, the outer layer of the largest
part of the brain and the brain's most expanded structure. Currently, around 6
in 10 children are still alive five years after they were diagnosed with a
malignant tumor of the central nervous system. Research into a better
understanding of how brain tumors arise and develop could help researchers in
finding possible targets for treatment.
To study the development of the brain and brain
tumors, scientists use organoids: 3D mini-organs or mini-tumors grown in the
lab. Scientists at the Princess Máxima Center and the Hubrecht Institute
created a new cortex organoid that better represents the human brain.
The new study led by dr. Benedetta Artegiani, research
group leader at the Máxima Center and Delilah Hendriks, Oncode-researcher at
the Hubrecht Institute and affiliated group leader at the Máxima Center, is published in Nature Communications.
The new cortex organoid that they generated more closely represents the human
brain in multiple aspects: their shape, their architectural organization and
several properties of their cells.
3D video of brain organoid showing in yellow the
stem cells and in magenta neurons. Credit: Benedetta Artegiani, Delilah
Hendriks, Anna Pagliaro
Recapitulate aspects of the developing human brain.
The formation of the human brain starts with a single structure, called the
neural tube, which is composed of a specific tissue, called the
neuroepithelium. The cells in this structure are then slowly 'instructed' to
generate all the different cells that are present in the various parts of the
brain.
Artegiani said, "The current brain organoid models generally have
several developmental structures acting like an 'independent' small developing
brain, within one organoid. Researchers have tried for a long time to mitigate
the formation of these multiple structures. To diminish variability, increase
reproducibility, better recreate the brain's different cellular identities, and
ultimately to recapitulate brain development more closely. Now in this
research, the new organoid model is composed of this self-organizing, single
developing neuroepithelium."
Anna Pagliaro, Ph.D., student and first author of the study, said, "We tried to mimic, in a dish, gradients of molecules that are present during brain development over time. This resulted in mini-brains that are very different in shape and structure than we used to work with. These organoids overall better resemble the early stages of brain development. It is quite impressive to see how much the shape of these organoids can influence all the different cells that form them, both in terms of their shape, architecture but also identity."
Image of novel
brain organoid model showing its characteristic convoluted shaped and extended
neuroepithelium. The neurons present in the organoid are shown in different
colors depending on their location within the tissue. Credit: Benedetta
Artegiani, Delilah Hendriks, Anna Pagliaro
Mimicking mechanisms of the human brain
The researchers named the new mini-brains expanded neuroepithelium
organoids (ENOs) for the developmental tissue used to grow them. To generate
them, they made a small but important change.
Hendriks said, "Cells in the brain are instructed to acquire their
identity through molecules that act slowly in time, the so-called temporal
gradients. This is exactly what we tried to mimic. To our surprise, it was
enough to just provide one of the molecules (TGF-b) slowly step-by-step to
generate brain organoids. This tiny change had an enormous impact and allowed
us to generate organoids with a shape and an identity more similar to the human
brain."
The next steps
Pediatric brain tumors may derive from unusual or mistaken developmental
processes and their study could benefit from these new models that better
recapitulate early embryonic developmental mechanisms. The signaling molecule
that the researchers used to make the organoids is often altered in childhood
brain tumors, also suggesting that the onset of cancer in young children could be
linked with changes in brain development.
Now that the researchers understand that temporal gradients are of great
importance in generating more accurate organoids, this study paves the way to
developing brain organoids more and more similar to the developing human brain.
3D imaging of
novel brain organoid viewed from different angles. The different colors
represent different cell types present in the organoid. Credit: Benedetta
Artegiani, Delilah Hendriks, Anna Pagliaro
Artegiani said, "We can use these novel organoids as a basis to model pediatric brain tumors, and study more in depth the role of TFG-b signaling in this process. Our research marks an essential step to create proper models to study pediatric brain cancer. If such a small change of a signaling molecule has such a great impact on brain organoid models, we can only start to imagine which effects small alterations during development can have for how pediatric brain tumors can develop."
by
Princess Máxima Center for Pediatric Oncology
Source: New strategies generate more accurate pediatric brain organoids (medicalxpress.com)
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