Breakthrough in Vascularized Organoids Promises Advances in Research and Regenerative Medicine

A breakthrough in growing blood vessel-containing organoids could revolutionize disease modeling, drug testing, and regenerative therapies, enabling larger and more mature tissue development.
Scientists at Stanford Medicine have achieved a significant milestone by cultivating organoids that contain functional blood vessel networks. These vascularized organoids, including models of the heart and liver, overcome previous size limitations that hindered their growth and maturation. Traditionally, organoids lack blood vessels, restricting their size to approximately the size of a sesame seed due to insufficient oxygen and nutrients reaching their core. This new approach employs optimized chemical recipes and biological techniques to generate organoids with branched, realistic blood vessels capable of supporting larger and more mature tissue development.
The research involved testing 34 different growth conditions based on combinations of growth factors and stem cell modifications to stimulate the formation of comprehensive cell types—including cardiomyocytes, endothelial cells, and smooth muscle cells—in cardiac organoids. The best recipe yielded organoids with organized internal structures resembling early-stage human hearts, containing up to 17 different cell types. Notably, these organoids demonstrate blood vessel systems that mirror the complexity of actual human tissues.
This advancement offers promising avenues for modeling early human development, drug testing, and regenerative therapies. For instance, vascularized cardiac organoids could be surgically implanted to repair damaged heart tissue, as they could connect seamlessly with the patient’s existing vasculature, improving survival and integration.
Furthermore, the techniques developed can be adapted to other organ models, like liver organoids with blood vessel networks, enhancing our ability to study organ development and disease more accurately. Future work aims to improve the maturity of these organoids and incorporate additional cell types such as immune and blood cells to better mimic adult tissues.
This pioneering work paves the way for more realistic and functional tissue models, advancing regenerative medicine and understanding of human development.
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