How To Trigger and Control Liver Regeneration

This article is a repost which originally appeared on SciTechDaily

WELLCOME TRUST/ CANCER RESEARCH UK GURDON INSTITUTE – AUGUST 17, 2021

Edited for content and readability
Images sourced from Pexels

DOI: 10.1016/j.stem.2021.07.002

Dresden and Cambridge researchers identify cell type that regulates liver regeneration with touch.

The human liver has the greatest regenerative capacity of any organ in the body and is able to regrow. Even from a 70% amputation, the regrowth has enabled live-donor transplants. Although the liver regenerates fully upon injury, the mechanisms that regulate how to activate or stop the process, are still unknown.  Researchers have now found that a regulatory cell type – mesenchymal cell – can activate or stop liver regeneration. The mesenchymal cells do so by the number of contacts they establish with the regenerating cells (epithelial cells).

This study suggests that mistakes in the regeneration process, which can give rise to cancer or chronic liver diseases, are caused by the wrong number of contacts between both populations. The work is in a paper published in the journal Cell Stem Cell on August 2^nd, 2021.

Approximately 29 million people in Europe suffer from a chronic liver condition such as cirrhosis or liver cancer. They are a major cause of morbidity and mortality with liver diseases accounting for approximately two million deaths per year worldwide. Currently, there is no cure and liver transplants are the only treatment for liver failure. Scientists are therefore exploring new options for how to trigger the regenerative capacity of the liver as an alternative means to restore function.

Development of mini-livers

Researchers at the Max Planck Institute of Molecular Cell Biology and Genetics in Dresden together with colleagues at the University of Cambridge’s Gurdon Institute study the biological principles of adult liver regeneration. In 2013, Meritxell Huch together with Prof Hans Clevers, developed the first liver organoids – miniature liver tissues generated from mouse liver cells in a dish in the lab. The researchers were even successful in transplanting the organoid into a mouse, where it was able to perform liver functions. In 2015, they successfully transferred this liver organoid technology to grow human liver in a dish from human liver biopsies. In 2017 they developed a similar system from human liver cancer.

A surprising, exciting observation

Two main functional cells of the adult liver are hepatocytes, which perform many of the liver’s functions, and ductal cells, which form the network of tiny ducts delivering bile to the intestine. These work in conjunction with other supporting cells, like the blood vessels or the mesenchymal cells. For building liver organoids, in the beginning the researchers only used ductal cells of the bile duct. In order to improve this model and make it more similar to the real liver, doctoral student Lucía Cordero-Espinoza and postdoctoral researcher Anna Dowbaj planned to build a more complex liver organoid that better mimics the cellular interactions and architecture of the adult liver tissue.

For that they added liver mesenchyme – a type of regulatory cell of the connective tissue, which support the tubular structure of the bile duct. “We put the mesenchymal cells next to the organoid, made out of the ductal cells, in a petri dish and saw that they were not touching or connecting, as they do in the native tissue” says Anna Dowbaj. The researchers contacted Florian Hollfelder at the University of Cambridge, who knew a method that enables combining the cells in tiny gels that allow them to meet and establish contact.

Anna continues: “We were excited to see how our new and more complex organoid was recapitulating the tissue architecture in a dish, so we decided to study how the cells behave and filmed them under a microscope. To our surprise, we saw a totally unexpected behavior: the tissue (organoid) shrunk on touch with the mesenchymal cells but grew in the absence of contacts. This contradicting behavior was very striking, but could help us explain why the tissue proliferated or stopped to do so during the regeneration process.”

Less is more and more is less

In a healthy liver, there is a defined number of contacts between the ductal cells and the mesenchymal cells, which tells the ductal cells not to make more of themselves and just stay as they are. Once the tissue experiences damage, the mesenchymal cells decrease their number of contacts with the ductal cells, so they can multiply to repair the damage. From their observation, the researchers concluded that rather than the absolute number of both cell types, it is the number of cellular contacts that controls how many cells are being produced to repair damaged tissue.

Too many touches by mesenchymal cells means that fewer or no new ductal cells are being produced, and fewer touches means that more cells are being produced. This regulation is very important because when there is no signal for ductal cells to stop reproducing themselves to repair tissue, there could be over-production, which could lead to cancer.

Meritxell Huch, who oversaw the study, concludes: “This is the first time that we were able to make those contacts visible and we have proven for the first time that they exist. We were able to do this because of our organoid systems. Even though we performed our experiments in a dish, outside of the living body, we think that the same process is taking place in the living organism. We have seen this in fixed points of time during the damage-regenerative process, but so far, we couldn’t observe this in the living organism because the technology is not available. While our study focuses on the ductal-mesenchymal interactions in the liver, we can imagine that similar mechanisms take place in any other system where cell numbers dynamically change, such as the lung or breast tissue. Of course, in the far future, we would like to create a liver organoid with all cell types. With such an organoid you could test drugs and see if these not only impact the regenerating cells but also their supportive environment. But for that, we need to wait until the technology is available.”