This newly discovered mechanism involves the molecules secreted by senescent liver cells – cells that have stopped multiplying – in liver disease patients. There was previous evidence that these secretions, known as senescence-associated secretory phenotype (SASP), drive recruitment of immune cells from the blood to the liver; but the molecular mechanisms of this were not clear. By studying samples of liver tissue from patients with liver disease and then setting up models in the laboratory to study immune cell recruitment, the research team have shown that these pathways involve an endothelial protein called plasmalemma vesicle-associated protein (PLVAP), which can support the recruitment of macrophages.
Birmingham researchers, including Professor Shishir Shetty, Alex Wilkinson and Daniel Patten, collaborated with international groups from the universities of Edinburgh, Cambridge, Minia (Egypt) and Turku (Finland), with funding from a Newton Prize, an annual award enabling international research partners to work together to address some of the world’s most pressing health and development issues.
Chronic liver disease is a global health burden accounting for approximately two million deaths each year worldwide. Ranking the second most common cause of premature death in the UK, chronic liver disease is also a major risk factor for developing hepatocellular carcinoma.
Study lead Shishir Shetty, Professor in Liver Tumour Immunology at the University of Birmingham’s Institute of Immunology and Immunotherapy, co-lead of the NIHR Birmingham Biomedical Research’s Inflammatory Liver Disease research theme, and Honorary Consultant Hepatologist at the Queen Elizabeth Hospital, commented: “Previous studies have shown that senescence in liver disease and liver cancer can be a double-edged sword. Our study highlights how we could potentially target blood vessels to prevent the detrimental consequences of senescence-driven inflammation whilst maintaining the protective effects of senescence, such as preventing malignant transformation of cells.”
