Organoids validated as tool for studying fetal intestine development

(Press-News.org) Developmental biologists have learned a great deal about how the human digestive tract functions through many years of studies involving fish, frogs, and rodents along with detailed explorations of individual human cells. But nothing quite matches the learning that could be achieved from studying actual human organ systems as they form.

Yet for obvious reasons, running experiments on growing human fetuses is both unethical and illegal.

Now a study led by researchers at Cincinnati Children’s, published online April 18, 2023, in the journal Development, reports that lab-grown tissues called organoids accurately mimic key development stages of the human intestine.

“Achieving this step is important because we know that many human conditions cannot be duplicated in animal models, nor can we learn everything we want to know from studying human cells that are not functioning together as a system. Now we have a source of functioning tissue that can be interrogated in many ways without involving any fetal tissue,” says the study’s corresponding author, Michael Helmrath, MD.

Helmrath is the director of surgical research at Cincinnati Children’s and co-director of the Center for Stem Cell and Organoid Medicine (CuSTOM). He has been working for more than a decade to study and improve intestine organoids for use in research and potentially for human transplantation.

In 2010, a team led by James Wells, PhD, at Cincinnati Children’s successfully used induced pluripotent stem cells to develop the world’s first functional human intestinal organoid. Wells, Helmrath and colleagues have been improving upon the model ever since, adding complexity by incorporating both the enteric nervous system and immune cells to reproduce the human intestine.

In their latest study, Helmrath, first author Akaljot Singh, an MD/PhD student, and 11 co-authors show that organoids transplanted into mice (to provide a blood supply and room to grow) follow the same temporal and spatial developmental steps that occur as intestines growing in a human fetus.

The team used RNA sequencing and other technologies to track the formation of specific cell types and key tissue structures grown for four weeks in a dish and then harvested at two, four, six, and eight weeks post-transplant. They show that the organoids in mice mimic human development that occurs from eight to 18 gestational weeks.

“Our findings suggest that tHIOs (transplanted human intestinal organoids) are a proxy for studying the development of the human fetal intestine. They mimic human fetal intestinal development on a morphological level, transcriptional level, and proteomic level,” the study states.

Why are intestine organoids important?

Our intestines do more than help digest our food. They play a central role in our immune response to harmful invaders. They also host populations of commensal (friendly) bacteria and fungi that influence our immune responses and our metabolisms.

Understanding more precisely how and when intestine development goes off-track could shed new light on many conditions, including birth defects, digestive disorders, obesity, and allergy risk. Both healthy intestinal organoids and versions exhibiting disease conditions can serve as improved test platforms to evaluate the safety and effectiveness of virtually any oral medication for any health problem.

Next steps

More research is needed to validate the organoid development model for certain subpopulations of cell types that were difficult to analyze in this study, Helmrath says.

But with the concept established that human organoids growing in mice can serve as a proxy for fetal development, Helmrath predicts a wave of studies to begin using them.

“This study has already identified several cell populations of interest that appear to play roles we did not recognize previously, including cells that appear to help guide muscle contraction, villi formation, and vascular development,” Helmrath says. “In the years to come, we expect tHIOs to support many more discoveries from many labs around the world.”

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