Every breath you take relies on a thin layer of cells inside your lungs that can be shredded by infections like COVID-19 or by inhaled toxins. When that lining—the epithelium—is badly damaged, the lung cannot repair itself properly, and no existing drug can fix it. This project aims to find out how the lung naturally rebuilds that lining, focusing on a type of immune cell called the interstitial macrophage. Researchers already know that macrophages flood into injured lungs and are essential for healing, but they do not know which specific subtype does the rebuilding or how it coordinates the process. Using human lung cells and laboratory models of injury, the team will map the signals that increase the number of these repair-promoting macrophages and the instructions they give to epithelial cells to regenerate. This is fundamental science. There is no immediate treatment to test. But understanding the precise cellular conversation between macrophages and lung lining cells could eventually lead to drugs that restart or accelerate regeneration after severe pneumonia, chemical inhalation, or ventilator-induced damage—conditions where current medicine can only support the patient and wait.
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Lungs are continually exposed to infections and toxins, which frequently damage the internal lining of the lungs, the epithelium. Widespread epithelial damage compromises lung function and occurs in fatal lung injury, including COVID-19 lung disease. It is therefore vital that the lung can regenerate and repair itself to ensure optimum functioning and protect against infections. But the regeneration process is very poorly understood and functions abnormally in several human lung conditions. No existing treatments promote lung regeneration. Understanding the process of how the lung naturally regenerates after injury may help develop new treatments that promote lung regeneration after serious infection or damage. It is known that following lung injury, cells from the body's immune system called macrophages increase in numbers and are critical to accelerate healing. But what sort of macrophage promotes epithelial regeneration and how they achieve this is not clear. This study will investigate which macrophages promote lung epithelial regeneration (focusing on 'interstitial macrophages'), how the numbers of these macrophages are increased after lung injury, and the methods these macrophages use to coordinate regeneration of the lung. This research will be achieved by laboratory-based investigation and involve using immune cells and epithelial cells isolated from human lungs and using models of lung injury and repair. The research will be carried out primarily by Dr Christopher Lucas, a consultant in respiratory medicine and researcher based at the University of Edinburgh. This work will be performed mainly at the newly formed Institute for Regeneration and Repair, the world's largest institute dedicated to tissue regeneration. The work will be supported by scientists at the University of Edinburgh, including Dr Jenkins, Dr Bain, Dr Gray and Prof. Walmsley who are world experts in macrophages and lung inflammation. Part of the work will also be delivered by national and international collaborations with the Carlin group at the Beatson UK, and the Perry Laboratory at Sloan Kettering in New York, USA, to benefit from those team's expertise in analysing immune cell responses. By using this unique combination of scientists, resources and novel research ideas we aim to identify new mechanisms of lung regeneration to help develop new treatments that will promote lung regeneration after serious infection or damage.
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