Back

In vitro cultivation techniques for modeling liver organogenesis, building assembloids, and designing synthetic tissues

Kumar, S.; Patel, H.; Parshurama, N.

2024-01-18 bioengineering
10.1101/2023.09.30.560154 bioRxiv
Show abstract

Chronic liver disease has reached epidemic proportions, affecting over 800 million people globally. The current treatment, orthotopic liver transplantation, has several limitations. Promising solutions have emerged in the field of liver regenerative medicine, with liver organogenesis holding significant potential. Early liver organogenesis, occurring between E8.5 and 11.5, involves the formation of epithelial-mesenchymal interactions leading to morphogenesis, hepatic cord formation, and collective migration. However, there is a lack of methods for in vitro modeling of this process. In this study, a detailed series of methods are presented enabling the modeling of various stages and aspects of liver organogenesis. In one method series, assembloid technology with hepatic and mesenchymal spheroids is utilized, replicating early structures found in liver organogenesis, modeling early morphogenesis, and demonstrating interstitial cell migration as seen in vivo. These innovative assembloid systems help identify factors influencing assembloid formation and migration. Hepatic spheroid cultivation systems were also employed to model collective migration and branching morphogenesis. Fibroblast-conditioned media (MES-CM) plays a significant role in initiating dose-dependent branching migration. Future work will involve high temporal and spatial resolution imaging of hepatic and mesenchymal interactions to determine the cascade of cellular and molecular events involved in tissue formation, morphogenesis, and migration. SUMMARYOrganoids revolutionize personalized tissue modeling for organ development, drug discovery, and disease research. Organoid engineering advances into creating intricate synthetic tissues. The aim is to integrate morphogenesis, assembloid technology, and biomatrices to advance tissue engineering. The presented methods aid in modeling liver organogenesis and establishing guidelines for synthetic tissue construction.

Matching journals

The top 8 journals account for 50% of the predicted probability mass.

50% of probability mass above

"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.