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Published on: April 3, 2017
Contribution of Macrophage Efferocytosis to Liver Homeostasis and Disease
Andrea Kristina Horst1, Gisa Tiegs1, Linda Diehl1
1Institute for Experimental Immunology and Hepatology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Abstract:
The clearance of apoptotic cells is pivotal for both maintaining tissue homeostasis and returning to homeostasis after tissue injury as part of the regenerative resolution response. The liver is known for its capacity to remove aged and damaged cells from the circulation and can serve as a graveyard for effector T cells. In particular Kupffer cells are active phagocytic cells, but during hepatic inflammatory responses incoming neutrophils and monocytes may contribute to pro-inflammatory damage. To stimulate resolution of such inflammation, myeloid cell function can change, via sensing of environmental changes in the inflammatory milieu. Also, the removal of apoptotic cells via efferocytosis and the signaling pathways that are activated in macrophages/phagocytes upon their engulfment of apoptotic cells are important for a return to tissue homeostasis. Here, we will discuss, how efferocytosis mechanisms in hepatic macrophages/phagocytes may regulate tissue homeostasis and be involved in tissue regeneration in liver disease.
Insights
Efficient clearance of apoptotic cells by liver macrophages is crucial for tissue homeostasis and regeneration. Efferocytosis, the process of engulfing dead cells, by hepatic phagocytes regulates these vital functions in liver disease.
Area of Science:
- Immunology
- Cell Biology
- Hepatology
Background:
- Apoptotic cell clearance is essential for tissue homeostasis and regeneration after injury.
- The liver removes aged and damaged cells, acting as a site for effector T cell clearance.
- While Kupffer cells are key phagocytes, inflammatory responses can involve neutrophils and monocytes, potentially causing damage.
Purpose of the Study:
- To discuss the role of efferocytosis mechanisms in hepatic macrophages and phagocytes.
- To explore how these mechanisms regulate tissue homeostasis in the liver.
- To investigate their involvement in liver disease and tissue regeneration.
Main Methods:
- Review of efferocytosis mechanisms in hepatic macrophages.
- Analysis of signaling pathways activated during efferocytosis.
- Discussion of environmental sensing by myeloid cells during inflammation.
Main Results:
- Efferocytosis by hepatic phagocytes is critical for resolving inflammation and restoring homeostasis.
- Changes in myeloid cell function, driven by inflammatory signals, promote resolution.
- Signaling pathways activated by apoptotic cell engulfment are key to tissue repair.
Conclusions:
- Efferocytosis mechanisms in liver phagocytes are central to maintaining tissue homeostasis.
- These mechanisms play a significant role in liver regeneration, particularly in the context of liver disease.
- Understanding efferocytosis is vital for developing strategies to promote liver repair.
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