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Updated: Aug 8, 2026

Static Adhesion Assay for the Study of Integrin Activation in T Lymphocytes
Published on: June 13, 2014
CD73 mediates adhesion of B cells to follicular dendritic cells
1National Public Health Institute, Turku University, Finland.
Insights
CD73, also known as ecto-5'-nucleotidase, mediates B cell adhesion to follicular dendritic cells (FDC). This interaction is crucial for B cell maturation within germinal centers, highlighting CD73's role in immune responses.
Area of Science:
- Immunology
- Cell Biology
Background:
- CD73 (ecto-5'-nucleotidase) is a lymphocyte marker involved in signaling, proliferation, and activation.
- Lymphocyte-vascular adhesion protein-2 was identified as CD73.
- CD73 mediates lymphocyte binding to endothelial cells.
Purpose of the Study:
- To investigate the role of CD73 in B cell-follicular dendritic cell (FDC) interactions.
- To determine if CD73 mediates adhesion between B cells and FDC.
Main Methods:
- In vitro aggregation assays using isolated germinal center B cells and FDC.
- Monoclonal antibody (MoAb) inhibition assay against CD73.
- Cytocentrifuge preparations and two-color immunofluorescence staining of tonsillar B-cell populations.
Main Results:
- A MoAb against CD73 inhibited the in vitro aggregation of germinal center B cells and FDC.
- CD73 is expressed on FDC and small, recirculating IgD+ B cells.
- Limited CD73 expression was observed on B cells within the germinal center.
Conclusions:
- CD73 mediates B cell adhesion to FDC.
- CD73 expressed on FDC plays a significant role in regulating B cell-FDC interactions.
- CD73 is implicated in controlling B cell maturation within germinal centers.
Abstract:
Lymphocyte-vascular adhesion protein-2 was recently identified as CD73. The CD73 molecule, otherwise known as ecto-5'-nucleotidase, is a lymphocyte maturation marker that is involved in intracellular signaling, and lymphocyte proliferation and activation. We now show that CD73, in addition to mediating lymphocyte binding to endothelial cells, also mediates adhesion between B cells and follicular dendritic cells (FDC), as a monoclonal antibody (MoAb) against CD73 inhibited the aggregation of isolated germinal center B cells and FDC in vitro. Cytocentrifuge preparations of isolated germinal center cells and two-color immunofluorescence stainings of different tonsillar B-cell populations show that CD73 is expressed on FDC and on small, recirculating IgD+ B cells, but only on a few B cells inside the germinal center. Thus, we propose that CD73 on FDC has an important role in controlling B cell-FDC interactions and B-cell maturation in germinal centers.
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