CINCINNATI—Scientists have successfully bioengineered human liver organoids that mimic key features of fatal liver disease in the laboratory, allowing them to uncover underlying disease biology in the organoids and test a potential therapy that in preclinical lab tests reversed an often-fatal childhood condition called Wolman disease.
In an article entitled “Modeling Steatohepatitis in Humans with Pluripotent Stem Cell-Derived Organoids,” published today in Cell Metabolism, researchers at Cincinnati Children’s Hospital Medical Center say their study overcomes major hurdles to understanding the molecular mysteries of liver diseases and finding much-needed new therapies. The research also leads to personalized methods to study inflammation and fibrosis in liver disease that match the unique genetics and biology of individual patients, according to the study authors.
“Although current human organoid systems can recreate organ architecture in living lab organisms like mice, they fail to capture the complex pathologies of inflammation and fibrosis in liver diseases,” said Takanori Takebe, M.D., lead study investigator and a physician at the Cincinnati Children’s Center for Stem Cell and Organoid Medicine (CuSTOM). “We developed a reproducible method to bioengineer complex, multicellular human liver organoids using pluripotent stem cells derived from healthy human donors and those with liver disease. These organoids generate different types of liver cells like hepatocytes, stellate and Kupffer-like cells, and they accurately recreate in the lab inflammation, fibrosis and other features of liver disease.”
This breakthrough is significant because years of attempted drug development for conditions like fatty liver disease (NASH, NAFLD, etc.) and Wolman have been hindered by a lack of human disease models that accurately mimic the diseases, noted Takebe. Although certain animal models like mice are available, they aren’t always reliable for studying human diseases.
The study is a collaboration of scientists at Cincinnati Children’s, the Institute of Research at Tokyo Medical and Dental University (TMDU) in Japan (where Takebe is also a member of the medical staff), and researchers at four other institutions in Japan and the United States.
One challenge of battling liver diseases is that they produce few initial symptoms that might prompt early, proactive medical treatment. Wolman disease is a genetic disorder that results in deficiency of an enzyme called lysosomal acid lipase (LAL) which breaks down fats in the body, according to the National Institutes of Health. Without the enzyme, fats over-accumulate in liver tissues and cause bloating, swelling of the stomach, vomiting and an enlarged liver or spleen, leading to life-threatening complications.
In nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH), fat accumulation, inflammation and fibrosis cause serious harm to the liver. The causes of NAFLD and NASH remain under investigation, although research points to certain health conditions that make fatty liver disease more likely, such as insulin resistance or obesity. Research also points to exposure to certain medications, toxins or diseases as potential but less common causes.
In this study, Takebe and his colleagues used 11 different lines of healthy and diseased pluripotent stem cells to generate complex multi-cellular human liver organoids. The diseased pluripotent cells included those grown from donors with a deficiency in the LAL protein. The researchers treated the organoids with free fatty acids — byproducts of fat metabolism in fatty tissue — which helped drive liver fat accumulation, inflammation and fibrosis. The organoids were able to recreate liver disease in the lab in a step-by-step, successive manner similar to Wolman disease in children.
As liver disease developed in the organoids, researchers used an extremely high-resolution imaging technology called atomic force microscopy. This allowed them to demonstrate and observe progressive levels of organ stiffening that they said confirms the increasing severity of accumulating liver fibrosis.
After concluding that Wolman disease in the human organoids was caused by LAL deficiency, researchers were able to reverse that deficiency by exposing the organoids to a recombinant LAL protein. Next, study authors leveraged earlier research that shows LAL deficiency causes over activation of a protein called mammalian target of rapamycin (mTOR), which is linked to liver fibrosis.
Previous research has shown that mTOR can be suppressed by a receptor protein called farnesoid X receptor (FXR), which functions in the nucleus of intestinal and liver cells. FXR is an acid that synthesizes a protein called fibroblast growth factor 19 (FGF19) in the ileum of the small intestine. FXR also upregulates and downregulates genes that control fat metabolism and bile acid processes. Takebe and his colleagues decided to treat the human liver organoids with Wolman disease with an FXR agonist called obeticholic acid.
FXR treatment suppressed fat accumulation in the human liver organoids and prolonged their survival. This opens the possibility of further preclinical testing to see whether or not FXR treatment might be an appropriate strategy for treating Wolman disease, the study investigators added. Because the study’s findings are preclinical and involve laboratory models, additional research is needed to show whether the findings will apply to clinical treatment in patients.