Adhesive bond dynamics in contacts between T lymphocytes and glass-supported planar bilayers reconstituted with the

M L Dustin1

  • 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.

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