Interdisciplinary approach uncovers new clues to triggers of gut inflammation
28 February 2019
New details about what happens when a key cellular process is impaired in cells that are vital for a healthy gut have been uncovered by a wide-ranging analysis.
Paneth cells are found at the bottom of crypts in the lining of the gut. They help defend against pathogenic microbes, as well as protecting the integrity of the lining of the gut. Carrying out these functions relies on them being able to secrete antimicrobial factors and other molecules that ensure a balanced gut microbiome and functioning stem cells that regenerate the gut lining. Given their vital role, it’s not surprising that abnormalities in Paneth cells are associated with gut conditions such as Crohn’s disease.
Similar symptoms are seen when a cellular process called autophagy is dysfunctional. Cells use autophagy to remove defective and potentially harmful proteins within themselves by surrounding the offending object in a membrane “bag” that is then tagged for destruction. Paneth cells also use this mechanism to bag up antimicrobial molecules for export from the cell in response to attack by pathogenic microbes.
This new study aimed to fill a gap in our understanding of the effects of autophagy impairment on Paneth cells, and was led by Dr Tamás Korcsmáros, a research fellow at the Earlham Institute and the Quadram Institute, which are strategically funded by the Biotechnology and Biological Sciences Research Council.
Tamas assembled an interdisciplinary team from across the Norwich Research Park to explore the molecular changes seen when autophagy in Paneth cells is blocked, and also what wider effects these changes might have. This involved integrating a number of different data sets and using network analysis and computational biology to interpret how these changes impact on different functions within cells.
Using cells from mice, the researchers grew organoid cultures in the lab. These are three dimensional collections of cells that grow and organise themselves into crypts, as they would in the lining of the gut. In some of these, a central gene needed for autophagy was knocked out. By comparison to organoids with the fully functioning gene, the team could then, for the first time, work out the molecular mechanisms and cellular processes affected by impaired autophagy in Paneth cells.
Firstly, the team measured the levels of all of the different proteins produced by the cells, and identified those proteins that changed in abundance depending on whether the autophagy gene was functional.
This identified over 280 proteins, which reflects the central importance of autophagy, but leads to the question of what functions these proteins have. To answer this, and find out what cellular functions are impaired when autophagy isn’t functioning, the researchers turned to network science and computational systems biology.
The scientific literature contains lots of data on the way individual proteins interact, their signalling pathways and their individual functions. Inside the cell, all of these processes are happening simultaneously, as part of complex networks of signals and instructions that maintain the cell and allow it to carry out its job. The researchers integrated a number of different networks and used the experimental data to link the proteins with altered abundances to their functions within these networks. This identified at least 18 cellular functions that are affected by autophagy.
Some of these were already known about, validating the approach, but others were previously unknown. Apoptosis, which allows damaged cells to kill themselves off, appears to be down-regulated in autophagy-impaired Paneth cells. As down-regulated apoptosis could keep damaged cells alive, this could explain the key mechanisms behind how chronic inflammatory diseases, such as Crohn’s Disease develop, so this could be an interesting area for further study. The system Paneth cells use to release antimicrobial compounds, exocytosis, is also down-regulated, which would affect the defence mechanism against microbial invasion.
Dr Tamás Korcsmáros at Earlham Institute, said, “To understand the causes of complex conditions like gut inflammation, we need to harness the power of network analysis in this way to integrate all of the available information. Using gut organoids and multi-omics analysis is an exciting and novel way to understand living systems. We hope that this study helps to shed new light on what triggers conditions like Crohn’s Disease, so we can find new ways of preventing or treating these conditions.”
Notes to editors
Further details appear in Disease Models and Mechanisms 2019.
For more information, please contact:
Dr Peter Bickerton
Scientific Communications & Outreach Manager, Earlham Institute (EI)
- +44 (0)1603 450 994
The Earlham Institute (EI) is a world-leading research Institute focusing on the development of genomics and computational biology. EI is based within the Norwich Research Park and is one of eight institutes that receive strategic funding from Biotechnology and Biological Science Research Council (BBSRC) - £5.43m in 2017/18 - as well as support from other research funders. EI operates a National Capability to promote the application of genomics and bioinformatics to advance bioscience research and innovation.
EI offers a state of the art DNA sequencing facility, unique by its operation of multiple complementary technologies for data generation. The Institute is a UK hub for innovative bioinformatics through research, analysis and interpretation of multiple, complex data sets. It hosts one of the largest computing hardware facilities dedicated to life science research in Europe. It is also actively involved in developing novel platforms to provide access to computational tools and processing capacity for multiple academic and industrial users and promoting applications of computational Bioscience. Additionally, the Institute offers a training programme through courses and workshops, and an outreach programme targeting key stakeholders, and wider public audiences through dialogue and science communication activities.
The Quadram Institute (quadram.ac.uk) is an interdisciplinary research centre at the forefront of a new era of food and health research. It brings together researchers and clinicians under one roof and houses one of Europe’s largest endoscopy units and a clinical trial facility. It focuses on lifelong health – from birth and throughout the lifecourse, increasing healthspan as well as lifespan. It undertakes both fundamental and translational research working with industry to accelerate innovation and bring novel therapeutics and new food products to patients and consumers.
Based on the Norwich Research Park, The Quadram Institute is a partnership between Quadram Institute Bioscience, the Norfolk and Norwich University Hospitals NHS Foundation Trust, the University of East Anglia and the Biotechnology and Biological Sciences Research Council (BBSRC).
Four interconnected interdisciplinary research themes in Quadram Institute Bioscience deliver a pipeline of research in plants, microbes, food and health: microbes in the food chain; the gut and the microbiome; food innovation and population health.