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Updated: Feb 4, 2026

Experimental Analysis of Apoptotic Thymocyte Engulfment by Macrophages
Published on: May 24, 2019
Effect of efferocytosis of apoptotic mesenchymal stem cells (MSCs) on C57BL/6 peritoneal macrophages function
Maryam Ghahremani Piraghaj1, Sara Soudi2, Hossein Ghanbarian3
1Department of Immunology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Abstract:
Phagocytic clearance of apoptotic cells (Efferocytosis) could affect the polarization of macrophages and promote M2 anti-inflammatory and regulatory phenotype and function. Here we tested the hypothesis that efferocytosis of apoptotic Adipose-Derived Mesenchymal Stem Cells (AD-MSCs) promotes macrophage M2 polarization. In this study, Macrophages were incubated with apoptotic MSCs and after 48 h interleukin-10 (IL-10), transforming growth factor-alpha (TNFα), and nitric oxide (NO) production were measured. Furthermore, phagocytosis ability and arginase activity were analyzed. The results showed that apoptotic MSCs could reduce TNFα and NO production, and increase IL-10 levels. Moreover, arginase activity and phagocytosis ability were also increased in tested macrophages compared to controls. In Conclusion efferocytosis of AD-MSCs can alter the macrophages phenotype toward regulatory and anti-inflammatory phenotype.
Insights
Phagocytic clearance of apoptotic Adipose-Derived Mesenchymal Stem Cells (AD-MSCs) promotes macrophage M2 polarization. This process enhances anti-inflammatory functions and regulatory capacity in macrophages.
Area of Science:
- Immunology
- Cell Biology
- Stem Cell Research
Background:
- Phagocytosis of apoptotic cells, known as efferocytosis, influences macrophage polarization.
- Macrophages can adopt M2 phenotypes, characterized by anti-inflammatory and regulatory functions.
Purpose of the Study:
- To investigate whether efferocytosis of apoptotic Adipose-Derived Mesenchymal Stem Cells (AD-MSCs) induces M2 polarization in macrophages.
- To assess the impact of AD-MSC efferocytosis on macrophage cytokine production, phagocytic capacity, and arginase activity.
Main Methods:
- Macrophages were incubated with apoptotic AD-MSCs.
- Interleukin-10 (IL-10), transforming growth factor-alpha (TNFα), and nitric oxide (NO) production were measured after 48 hours.
- Phagocytosis ability and arginase activity were subsequently analyzed.
Main Results:
- Apoptotic AD-MSCs significantly reduced TNFα and NO production by macrophages.
- A notable increase in IL-10 levels was observed in macrophages after efferocytosis.
- Enhanced phagocytosis ability and increased arginase activity were detected in macrophages.
Conclusions:
- Efferocytosis of AD-MSCs effectively shifts macrophage phenotype towards a regulatory and anti-inflammatory profile.
- This interaction highlights a mechanism by which MSCs modulate the immune microenvironment.
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