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Updated: Dec 28, 2025

Isolation, Characterization, and Purification of Macrophages from Tissues Affected by Obesity-related Inflammation
Published on: April 3, 2017
Macrophage Phenotype and Function in Liver Disorder
Lang Dou1,2,3, Xiaomin Shi1,2,3, Xiaoshun He1,2,3
1Organ Transplantation Center, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Abstract:
Hepatic macrophages are a remarkably heterogeneous population consisting of self-renewing tissue-resident phagocytes, termed Kupffer cells (KCs), and recruited macrophages derived from peritoneal cavity as well as the bone marrow. KCs are located in the liver sinusoid where they scavenge the microbe from the portal vein to maintain liver homeostasis. Liver injury may trigger hepatic recruitment of peritoneal macrophages and monocyte-derived macrophages. Studies describing macrophage accumulation have shown that hepatic macrophages are involved in the initiation and progression of various liver diseases. They act as tolerogenic antigen-presenting cells to inhibit T-cell activation by producing distinct sets of cytokines, chemokines, and mediators to maintain or resolve inflammation. Furthermore, by releasing regenerative growth factors, matrix metalloproteinase arginase, they promote tissue repair. Recent experiments found that KCs and recruited macrophages may play different roles in the development of liver disease. Given that hepatic macrophages are considerably plastic populations, their phenotypes and functions are likely switching along disease progression. In this review, we summarize current knowledge about the role of tissue-resident macrophages and recruited macrophages in pathogenesis of alcoholic liver disease (ALD), non-alcoholic steatohepatitis (NASH), viral hepatitis, and hepatocellular carcinoma (HCC).
Insights
Hepatic macrophages, including Kupffer cells (KCs) and recruited types, play diverse roles in liver diseases like ALD, NASH, viral hepatitis, and HCC. Their plasticity influences disease progression and outcomes.
Area of Science:
- Immunology
- Hepatology
- Cell Biology
Background:
- Hepatic macrophages are heterogeneous, comprising resident Kupffer cells (KCs) and recruited macrophages from the peritoneum and bone marrow.
- KCs maintain liver homeostasis by scavenging microbes, while recruited macrophages contribute to liver injury and disease progression.
- These macrophages exhibit plasticity, altering phenotypes and functions during disease development.
Purpose of the Study:
- To review the distinct roles of tissue-resident and recruited hepatic macrophages in liver disease pathogenesis.
- To explore the involvement of hepatic macrophages in Alcoholic Liver Disease (ALD), Non-Alcoholic Steatohepatitis (NASH), viral hepatitis, and Hepatocellular Carcinoma (HCC).
Main Methods:
- Literature review summarizing current knowledge on hepatic macrophage populations.
- Analysis of studies investigating macrophage accumulation and function in various liver pathologies.
Main Results:
- Hepatic macrophages are implicated in the initiation and progression of diverse liver diseases.
- They function as tolerogenic antigen-presenting cells, modulating T-cell responses and inflammation.
- Macrophages release factors promoting tissue repair and regeneration, but can also contribute to disease pathology.
Conclusions:
- Both Kupffer cells and recruited macrophages have distinct, yet crucial, roles in liver disease development.
- Understanding macrophage plasticity is key to comprehending their dynamic involvement in liver pathogenesis.
- Targeting hepatic macrophages may offer therapeutic strategies for liver diseases.
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