Credit:
Pixabay/CC0 Public Domain
Researchers at
the Francis Crick Institute and AlveoliX have developed the first human
lung-on-chip model using stem cells taken from only one person. These chips
simulate breathing motions and lung disease in an individual, holding promise
for testing treatments for infections like tuberculosis (TB) and delivering
personalized medicine.
The research is published in the journal Science
Advances.
Air sacs in the lungs called alveoli are the essential
site of gas exchange and also an important barrier against inhaled viruses and
bacteria that cause respiratory diseases like flu or TB.
Researchers have been working to recreate the battle
between human cells and bacteria in the lab by building a lung-on-a-chip: small
units of human lung on a plastic chip containing tiny channels and
compartments. In this case, they aimed to recreate air sacs to understand how
they respond to infection.
Until now, these lung-on-chip devices have been made
of a mixture of patient-derived and commercially available cells, meaning they
can't fully replicate the lung function or disease progression of a single
individual.
In the study, the team at the Crick developed a new lung-on-chip model that contains only genetically identical cells derived from stem
cells from a single donor.
Based on a protocol developed previously by the lab,
the team produced type I and II alveolar epithelial cells and vascular
endothelial cells from human-induced pluripotent stem cells, cells that can
virtually become any cell in the body. These epithelial and endothelial cells
are separately grown on the top and bottom of a very thin membrane in a device
manufactured by biotechnology company AlveoliX to recreate an air sac barrier.
To further simulate the human lung, AlveoliX has designed specialized machines to impose rhythmic
three-dimensional stretching forces on the recreated air sac barrier, mimicking
the motion of breathing. This stimulates the formation of microvilli, a key
feature of alveolar epithelial cells, to increase surface area for lung
functions (image).
Next, the scientists added immune cells called
macrophages into the chip, again produced from the stem cells of the same
donor, before adding TB bacteria to simulate the early stages of the disease.
In the chips infected with TB, the team reported large macrophage clusters containing necrotic cores, a group of dead macrophages in the
center, surrounded by live macrophages. Eventually, five days after infection,
the endothelial and epithelial cell barriers collapsed, showing that the air
sac function had broken down.
Max Gutierrez, Principal Group Leader of the
Host-Pathogen Interactions in Tuberculosis Laboratory at the Crick and senior
author, said, "Given the increasing need for non-animal technologies, organ-on-chip approaches are becoming ever more important to recreate
human systems, avoiding differences in lung anatomy, makeup of immune cells and
disease development between animals and humans.
"Composed of entirely genetically identical
cells, the chips could be built from stem cells from people with particular
genetic mutations. This would allow us to understand how infections like TB
will impact an individual and test the effectiveness of treatments like
antibiotics."
Jakson Luk, Postdoctoral Fellow in the Host-Pathogen
Interactions in Tuberculosis Laboratory and first author, said, "TB is a
slow-moving disease, with months between infection and the development of
symptoms, so there's an increasing need to understand what's happening in the
unseen early stages.
"We were successfully able to mimic these initial events in TB progression, giving a holistic picture of how different lung cells respond to infections. We're excited that the new model could be applied to a huge range of research, such as other respiratory infections or lung cancer, and we're now looking at refining the chip by incorporating other important cell types."
Source: First breathing 'lung-on-chip' developed using genetically identical cells

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