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Reference: https://app.jove.com/t/2757/a-simple-... A straightforward and effective approach has been developed for the isolation of macrophages from mixed primary cultures of adult liver cells. This method addresses the challenges often encountered in separating macrophages from other cell types present in the liver, which can complicate subsequent analyses and experiments. By utilizing specific techniques that enhance the purity and yield of macrophages, researchers can obtain a more homogeneous population, thereby facilitating a deeper understanding of their functions and roles within the hepatic environment. The process begins with the careful preparation of liver cell cultures, ensuring that the conditions are optimal for the growth and maintenance of the various cell types present. Following this, a series of selective isolation techniques are employed, which may include density gradient centrifugation or magnetic-activated cell sorting (MACS). These techniques leverage the unique surface markers expressed by macrophages, allowing for their effective separation from hepatocytes and other non-parenchymal cells. The result is a highly enriched population of macrophages that can be used for further study, including functional assays and gene expression analyses. In addition to enhancing the purity of isolated macrophages, this method also emphasizes the importance of maintaining cell viability throughout the isolation process. By minimizing stress and damage to the cells, researchers can ensure that the macrophages retain their functional characteristics, which is crucial for accurate experimental outcomes. This innovative approach not only streamlines the isolation process but also opens new avenues for research into liver immunology and the role of macrophages in liver diseases, ultimately contributing to the advancement of therapeutic strategies.