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Saturday, April 13, 2024

Scientists Grew Mini Human Guts Inside Mice

Your gut has an obvious job: It processes the food you eat. But it has another important function: It protects you from the bacteria, viruses, or allergens you ingest along with that food. “The largest part of the immune system in humans is the GI tract, and our biggest exposure to the world is what we put in our mouth,” says Michael Helmrath, a pediatric surgeon at Cincinnati Children’s Hospital Medical Center who treats patients with intestinal diseases. 

Sometimes this system malfunctions or doesn’t develop properly, which can lead to gastrointestinal conditions like ulcerative colitis, Crohn’s disease, and celiac—all of which are on the rise worldwide. Studying these conditions in animals can only tell us so much, since their diets and immune systems are very different from ours.

In search of a better method, last week Helmrath and his colleagues announced in the journal Nature Biotechnology that they had transplanted tiny, three-dimensional balls of human intestinal tissue into mice. After several weeks, these spheres—known as  organoids—developed key features of the human immune system. The model could be used to mimic the human intestinal system without having to experiment on sick patients.

The experiment is a dramatic follow-up from 2010, when researchers at Cincinnati Children’s became the first in the world to create a working intestine organoid—but their initial model was a simpler version in a lab dish. A few years later, Helmrath says, they realized “we needed it to become more like human tissue.” Scientists elsewhere are growing similar miniature replicas of other human organs—including the brain, lung, and liver—to better understand how they develop normally and how things go awry to give rise to disease. Organoids are also being used as human avatars for drug testing. Since they contain human cells and display some of the same structures and functions as real organs, some researchers think they’re a better stand-in than lab animals.

“It’s incredibly important that when we are trying to create these platforms for testing drug efficacy and drug side effects in human tissue models that we actually make sure that we are as close to, and as complete as, the tissue in which the drug will work eventually in our human body. So, adding the immune system is an important part of that,” says Pradipta Ghosh, director of the Humanoid Center of Research Excellence at the University of California San Diego School, which is developing human organoids to screen and test drugs. Ghosh was not involved in the study.

To grow the organoid, the scientists started with induced pluripotent stem cells, which are created from mature human cells drawn from blood or skin. These have the ability to turn into any type of body tissue. By feeding the stem cells a specific molecular cocktail, the team coaxed them into intestinal cells. After growing for 28 days in a dish, the cells formed spheres of tissue just a few millimeters in diameter. 

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The team carefully transplanted these spheres into mice that had been genetically engineered to suppress their own immune systems so that the organoid tissue would not be rejected. (The researchers transplanted the intestinal organoid next to each mouse’s kidneys, so it wasn’t actually connected to the animals’ digestive tracts.) To stimulate the organoids into producing human immune cells, they had previously given the mice human cord blood—a source of stem cells that could transform into the desired cells. 

After 20 weeks, the organoids had each grown to the size of a pea and contained around 20 types of human immune cells. “That is very similar to the populations we see in the human gut,” says Helmrath. At that point, the organoids had also formed human lymphoid follicles, or Peyer’s patches, important structures in the intestine that keep pathogens at bay by maintaining levels of healthy bacteria. 

These structures, Ghosh says, are like tonsils for the gut: They stop germs from making us sick. Other researchers have added immune cells to organoids made in a lab dish, but Ghosh says the Cincinnati team is unique in taking the extra steps of transplanting them into an animal so they develop working parts of a human immune system, including versions of these follicles. 

To test whether the immune cells were functional, the researchers exposed the organoids to E. Coli bacteria, which is commonly found in the human intestine. Afterward, they found that the Peyer’s patches produced M cells, immune signaling cells found in the lining of the gut. Helmrath says this indicates that the organoids’ immune system could respond to the presence of bacteria. Previous studies have shown that infection and inflammation spur the production of M cells. 

 Matthew Grisham, a gastroenterologist at Texas Tech University Health Sciences Center who wasn’t involved in the new study, says the findings are exciting because these structures have a “human immune cell composition very similar to that of the developing human gut.” He says the organoid model will help researchers investigate the mechanisms responsible for intestinal infection, inflammation, and food allergies.

The Cincinnati researchers also hope their organoids could one day be used to treat people born with genetic defects that affect their digestive systems, or those who have lost intestinal function to cancer or inflammatory bowel diseases. 

That these organoids can flourish in a mouse is an encouraging sign that they might be able to grow on their own if transplanted into a person. Using induced pluripotent stem cells taken from patients, scientists could perhaps one day make customized tissue patches to help heal damaged organs. 

In the near-term, Helmrath says his team plans on making organoids from patients’ own cells to test out possible individualized therapies. “This is right around the corner,” he says.

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