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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
Adhesive bond dynamics in contacts between T lymphocytes and glass-supported planar bilayers reconstituted with the
1Center for Immunology and the Department of Pathology, Washington University School of Medicine, Box 8118, St. Louis, Missouri 63110, USA. dustin@pathbox.wustl.edu
Insights
The T cell glycoprotein CD2 and its ligand CD58 form transient bonds in cell contact areas, with rapid dissociation and partner exchange, similar to solution behavior. This contrasts with slower Fc receptor-IgG interactions.
Area of Science:
- Immunology
- Cell Biology
- Biophysics
Background:
- The T cell glycoprotein CD2 interacts with its ligand CD58, crucial for T cell interactions.
- Solution measurements indicate a low-affinity, fast off-rate for CD2-CD58 binding, but in vivo relevance is unclear.
Purpose of the Study:
- To investigate the transient nature of CD2-CD58 bonds within cell contact areas.
- To compare the CD2-CD58 interaction dynamics with Fc receptor-IgG interactions.
Main Methods:
- Utilized fluorescence photobleaching recovery and molecular accumulation in T cell-planar bilayer contact areas.
- Measured the replacement rate of bleached CD58 in the contact zone by fluorescent CD58 from surrounding regions.
Main Results:
- Rapid recovery of fluorescence in the contact area demonstrated transient CD2-CD58 bonds with rapid dissociation and partner exchange.
- CD2-CD58 bond dissociation dynamics in contact areas mirrored solution off-rate measurements.
- Fc receptor-IgG interactions showed a 10-fold slower recovery, indicating a longer bond lifetime compared to CD2-CD58.
Conclusions:
- CD2-CD58 bonds are transient in cell contact areas, supporting the validity of solution off-rate data.
- The transient nature of CD2-CD58 interactions has implications for T cell signaling and cell detachment mechanisms.
- Fc receptor-IgG interactions exhibit significantly longer bond lifetimes than CD2-CD58 interactions.
Abstract:
The interaction of the T cell glycoprotein CD2 and its ligand CD58 is important for T cell interaction with antigen-presenting and target cells. The binding interaction is of low affinity and has a fast off-rate (>5 s-1) in solution. However, solution measurements may not accurately predict the behavior of molecules in an adhesive contact area. Interaction between T cells that express CD2 and glass-supported planar bilayers containing purified and fluorescently labeled CD58 leads to accumulation of CD58 (fluorescence) in the cell/bilayer contact area. CD58 molecules accumulated within the contact area in excess of the CD58 density in the bilayer outside the contact area can be considered as bound by cell surface CD2. Here, this phenomena and fluorescence photobleaching recovery were utilized to determine whether CD2-CD58 bonds are transient in contact areas. Fluorescent CD58 molecules accumulated in the T cell-bilayer interface were completely bleached. The bleached CD58 molecules accumulated in the contact area were rapidly replaced by fluorescent CD58 that diffused into the contact area from adjacent bilayer regions outside the contact area. Rapid recovery of the accumulated fluorescence directly demonstrates that the CD2-CD58 bonds are dissociating and that the dissociation leads to partner exchange, rather than rebinding of the same CD2-CD58 pairs. This suggests that the solution off-rate provides an accurate description of CD2-CD58 interaction in contact areas. Accumulated fluorescent IgG in contacts between K562 cells expressing low affinity Fc receptors and planar bilayers with fluorescent IgG bound to hapten-derivitized phospholipids displayed slower recovery than CD58 by a factor of 10. This suggests that the Fc receptor-IgG interaction has a longer lifetime than the CD2-CD58 interaction. These findings have implications for the mechanism of signaling by CD2 and the mechanism of cell detachment from large numbers of transient interactions.
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