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Imaging G Protein-coupled Receptor-mediated Chemotaxis and its Signaling Events in Neutrophil-like HL60 Cells
Published on: September 14, 2016
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CAP37, a human neutrophil-derived chemotactic factor with monocyte specific activity
H A Pereira1, W M Shafer, J Pohl
1Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia 30322.
The Journal of Clinical Investigation
|May 1, 1990
Summary
Neutrophil antimicrobial protein CAP37 (calgranulin A) attracts monocytes during inflammation. Released during phagocytosis, CAP37 may recruit monocytes in the second inflammatory wave.
Area of Science:
- Immunology
- Biochemistry
Background:
- CAP37 is an antimicrobial protein found in human neutrophil granules.
- It plays a role in inflammatory processes.
Purpose of the Study:
- To investigate the chemotactic properties of CAP37 for different immune cells.
- To explore the potential role of CAP37 in inflammatory responses.
Main Methods:
- Purification of CAP37 using sequential chromatography (carboxymethyl Sephadex, G-75 Sephadex, hydrophobic interaction HPLC).
- Chemotaxis assays using human and rabbit mononuclear cells, neutrophils, and lymphocytes.
- Sequence analysis of the N-terminus of CAP37.
- Inhibition assays using diisopropyl fluorophosphate.
- Observation of CAP37 release during Staphylococcus aureus phagocytosis by neutrophils.
Main Results:
- Purified CAP37 is a potent chemoattractant for human monocytes at nanomolar concentrations, comparable to formyl-methionyl-leucyl-phenylalanine.
- CAP37 lacks chemotactic activity for neutrophils and lymphocytes but shows chemokinetic effects.
- CAP37 is also chemotactic for rabbit mononuclear cells, requiring higher concentrations.
- Sequence analysis suggests CAP37 lacks serine protease activity.
- Significant extracellular release of CAP37 from neutrophils occurs during Staphylococcus aureus phagocytosis.
Conclusions:
- CAP37 acts as a specific chemoattractant for monocytes.
- Neutrophil-derived CAP37 released during phagocytosis may orchestrate monocyte recruitment in inflammatory responses.
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