Characterization of cytoadhesion molecules on human monocytes and tissue macrophages
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Updated: Sep 14, 2026

Quantitation of Endothelial Cell Adhesiveness In Vitro
Published on: June 18, 2015
1Department of Pathology and Surgery, Ullevål University Hospital, Oslo, Norway.
Abstract:
The presence of proteins antigenically related to the GPIIb/IIIa complex expressed on platelets have been investigated on tissue macrophages recovered by bronchoalveolar lavage (lung alveolar macrophages, LAM) or peritoneal lavage (peritoneal macrophages, PM) as well as on monocytes. Polyclonal antibodies (pab) directed against human platelet GPIIb/IIIa and the vitronectin receptor (VnR), and mouse monoclonal antibodies (mab) against human GPIIb, GPIIIa or the GPIIb/IIIa-complex were used. Triton X-100 extracts of bronchoalveolar cells (BAC) (containing 94% LAM) and the ultrasedimentable fraction of cell-free bronchoalveolar lavage (US) reacted with the polyclonal antibodies against the GPIIb/IIIa-complex and the VnR, but only with one (P4) of the mabs. Cell microscopy after immunogold labelling and alkaline phosphatase immunostaining, as well as immunofluorescence using the P4 mab and the polyclonal anti-GPIIb/IIIa clearly demonstrated positive membrane staining of LAM, PM and monocytes. Both BAC and US extracts gave rise to immunoprecipitates in crossed and rocket immunoelectrophoresis using anti-GPIIb/IIIa and anti-VnR. Our data indicate that monocytes and their monocyte-derived tissue counterparts constitutively express GPIIb/IIIa-like antigen(s) on their membrane. The presence of such antigen(s) on tissue macrophages makes it unlikely that platelet contamination is responsible for these findings.
Insights
Monocytes and tissue macrophages, including lung alveolar macrophages (LAM) and peritoneal macrophages (PM), express proteins similar to platelet GPIIb/IIIa. This suggests these antigens are constitutively present on monocytes and their tissue-derived macrophages.
Area of Science:
- Immunology
- Cell Biology
- Hematology
Background:
- Platelets express the GPIIb/IIIa complex, crucial for aggregation.
- Tissue macrophages are derived from monocytes.
- The expression of platelet-related antigens on macrophages is not well understood.
Purpose of the Study:
- To investigate the presence of GPIIb/IIIa-like antigens on lung alveolar macrophages (LAM), peritoneal macrophages (PM), and monocytes.
- To determine if these antigens are expressed constitutively on monocytes and their tissue-derived macrophages.
Main Methods:
- Used polyclonal and monoclonal antibodies against human platelet GPIIb/IIIa and vitronectin receptor (VnR).
- Analyzed bronchoalveolar lavage cells (BAC) and ultrasedimentable fractions (US) using immunogold labeling, alkaline phosphatase immunostaining, immunofluorescence, and immunoprecipitation techniques.
- Examined LAM, PM, and monocytes.
Main Results:
- Bronchoalveolar cells (BAC) and ultrasedimentable fractions (US) reacted with anti-GPIIb/IIIa and anti-VnR antibodies.
- Positive membrane staining for GPIIb/IIIa-like antigens was observed on LAM, PM, and monocytes.
- Immunoprecipitation confirmed the presence of these antigens in BAC and US extracts.
Conclusions:
- Monocytes and their tissue-derived macrophages (LAM, PM) constitutively express GPIIb/IIIa-like antigens on their membranes.
- The findings suggest these antigens are intrinsic to monocytes and macrophages, not due to platelet contamination.
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