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Published on: May 31, 2018
The scavenger receptor CD36 plays a role in cytokine-induced macrophage fusion
Laura Helming1, Julia Winter, Siamon Gordon
1Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.
Abstract:
Multinucleated giant cells, characteristic of granulomatous infections, originate from the fusion of macrophages. Using an antibody screening strategy we found that the scavenger receptor CD36 participates in macrophage fusion induced by the cytokines IL-4 and GM-CSF. Our results demonstrate that exposure of phosphatidylserine on the cell surface and lipid recognition by CD36 are required for cytokine-induced fusion of macrophages. We also show that CD36 acts in a heterotypic manner during giant-cell formation and that the formation of osteoclasts is independent of CD36. The discovery of molecules involved in the formation of multinucleated giant cells will enable us to determine their functional significance. Furthermore, our results suggest that lipid capture by cell surface receptors may be a general feature of cell fusion.
Insights
The scavenger receptor CD36 is crucial for cytokine-induced macrophage fusion, a process vital for forming multinucleated giant cells in infections. This fusion requires cell surface lipid exposure and CD36
Area of Science:
- Immunology
- Cell Biology
- Infectious Diseases
Background:
- Multinucleated giant cells are hallmarks of granulomatous infections.
- These cells form through the fusion of macrophages.
Purpose of the Study:
- To identify molecular mechanisms underlying cytokine-induced macrophage fusion.
- To investigate the role of scavenger receptor CD36 in giant cell formation.
Main Methods:
- Antibody screening strategy to identify key molecules.
- Analysis of phosphatidylserine exposure and lipid recognition.
- Assessment of CD36's role in heterotypic fusion and osteoclast formation.
Main Results:
- The scavenger receptor CD36 mediates macrophage fusion induced by IL-4 and GM-CSF.
- Cytokine-induced fusion necessitates phosphatidylserine exposure and CD36-mediated lipid recognition.
- CD36 functions heterotypically in giant cell formation, but not in osteoclast development.
Conclusions:
- CD36 is a key mediator of cytokine-induced macrophage fusion.
- Lipid capture by cell surface receptors may be a general mechanism for cell fusion.
- Understanding these pathways can elucidate the functional significance of multinucleated giant cells.
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